CSS Tabs
References
Albumin
Depletion
AlbuSorb™
Albumin Depletion Kit
Intestinal Organoid Supernatants
Jordan, Christine KI, et al. "Symbiotic Firmicutes establish mutualism with the host via innate tolerance and resistance to control systemic immunity.."
Cell Host & Microbe
(2023).
Intestinal Organoid Supernatants
Matsuzawa-Ishimoto, Yu, et al. "The γδ IEL effector API5 masks genetic susceptibility to Paneth cell death.."
Nature
(2022): 1-8.
Human serum
High-throughput, Automated INTip™ SPE Combined with AlbuSorb™ Products for Efficient Albumin and Albumin/IgG Depletion Matthew Fitts 1; William E. Kemnitzer 1; Paul Meeh 1; Matt Kuruc 2; Swapan Roy 2; Sowmya Avadhani 2
1DPX Technologies, Columbia, SC; 2Biotech Support Group LLC, Monmouth Junction, NJ Corresponding Author: mkuruc@biotechsupportgroup.com
Clarified serum
A Preliminary Investigation Using Targeted LC-MS Proteomic Methods Demonstrates Unique Serum Profiles of Hospitalized SARS-CoV-2 Patients Douglas D Fraser 1; Haiyan Zheng 2; Swapan Roy 3; Matt Kuruc 3; Amenah Soherwardy 2; Devjit Roy 4; Sowmya Avadhani 3
1Lawson Research Institute, London, Ontario; 2Rutgers University Proteomics Center, Piscataway, New Jersey; 3Biotech Support Group LLC, Monmouth Junction, NJ; 4Nathan Littauer Hospital, Gloversville, New York Corresponding Author : mkuruc@biotechsupportgroup.com
Whole blood, serum and plasma samples
DPX Technologies and Biotech Support Group Announce In-Market Partnership for High Throughput Proteomic Sample Prep
Serum
Exosomes
Valladolid-Acebes, Ismael, et al."Lowering apolipoprotein CIII protects against
high-fat diet–induced metabolic derangements.."
Science Advances
7.11 (2021): eabc2931.
Serum
Exosomes
Chettimada,
Sukrutha, et al. "Exosome
markers associated with immune activation and oxidative stress in HIV
patients on antiretroviral therapy."
Scientific
Reports
8.1 (2018): 7227.
Cerebrospinal
Fluid
Gwenael
Pottiez, Pawel Ciborowski.
Proteomic
Profiling of Cerebrospinal Fluid Expression Profiling In
Neuroscience
Neuromethods.2012;64:245-270
Synovial
fluid
Happonen
KE, Fürst CM, Saxne T et al.
PRELP
protein inhibits the formation of the complement membrane attack
complex
.
Journal of Biological Chemistry.2012;287(11):8092-100
Serum
Vialaret, Jerome & Kadi, Sarah & Tiers, Laurent & O Flynn, Robin & Lehmann, Sylvain & Hirtz, Christophe. (2018).
"Albumin depletion of human serum to improve quantitative clinical proteomics."
Current Topics in Peptide & Protein Research 19. 53-62.
Roy, Swapan, and Matthew Kuruc.
"Methods to Monitor
the Functional Subproteomes of SERPIN Protease Inhibitors.
Functional Proteomics. Humana Press, New York, NY, 2019. 41-54
Berggren,
Per-olof, and Lisa Juntti-berggren.
"Methods
for treating and/or limiting development of diabetes." U.S.
Patent No. 20,170,037,118. 9 Feb. 2017
.MOJ
Proteomics Bioinform 2016, 3(6): 00106
Swapan
Roy, Matthew Kuruc.
The
Functional Subproteomes of Serpin Protease Inhibitors are Now Open
for LC-MS Biomarker Discovery
.MOJ
Proteomics Bioinform 2016, 3(6): 00106
Holmberg
R, Refai E, Höög A.
Lowering
apolipoprotein CIII delays onset of type 1 diabetes
.
Proceedings of the National Academy of Sciences.2011;108(26):10685-9.
Tang
MX, Ogawa K, Asamoto M.
Effects
of Nobiletin on PhIP-Induced Prostate and Colon Carcinogenesis in
F344 Rats
Nutrition
and Cancer.2011;63(2):227-33
Holmberg,
Rebecka
Apolipoprotein
CIII and Ljungan virus in diabetes
2010.
Doctoral Thesis
Lu
Q, Zheng X, McIntosh T
Development
of different analysis platforms with LC-MS for pharmacokinetic
studies of protein drugs
.
Analytical Chemistry.2009;81(21):8715-23
Urine
Zubiri,
Irene, et al. "
Diabetic
nephropathy induces changes in the proteome of human urinary exosomes
as revealed by label-free comparative analysis
."
Journal of proteomics 96 (2014): 92-102.
Patent
Berggren,
Per Olaf, Yang, Shao-Nian. 2012.
Methods
For Treating And/Or Limiting Development Of Diabetes
.
U.S. Patent 20120328630 Kind Code: A1, filed June 25, 2012, and
issued December 27, 2012.
AlbuTrial™
Kit - AlbuVoid™ and AlbuSorb™
Cerebrospinal
Fluid
Gwenael
Pottiez, Pawel Ciborowski.
Proteomic
Profiling of Cerebrospinal Fluid Expression Profiling In
Neuroscience
Neuromethods.2012;64:245-270
Synovial
fluid
Happonen
KE, Fürst CM, Saxne T et al.
PRELP
protein inhibits the formation of the complement membrane attack
complex
.
Journal of Biological Chemistry.2012;287(11):8092-100
Serum
Holmberg
R, Refai E, Höög A.
Lowering
apolipoprotein CIII delays onset of type 1 diabetes.
Proceedings
of the National Academy of Sciences.2011;108(26):10685-9.
Tang
MX, Ogawa K, Asamoto M.
Effects
of Nobiletin on PhIP-Induced Prostate and Colon Carcinogenesis in
F344 Rats
Nutrition
and Cancer.2011;63(2):227-33
Holmberg,
Rebecka
Apolipoprotein
CIII and Ljungan virus in diabetes
2010.
Doctoral Thesis
Lu
Q, Zheng X, McIntosh T
Development
of different analysis platforms with LC-MS for pharmacokinetic
studies of protein drugs
.
Analytical Chemistry.2009;81(21):8715-23
AlbuVoid™
References
Conditioned media
Paulsen, Bruna, et al."Reproducible differentiation of pure ovarian support cells from clinical-grade hiPSCs as a novel infertility treatment."
bioRxiv (2024): 2024-04.
Tumor-stroma ratio
Polack, M., et al. "Results from the UNITED study: a multicenter study validating the prognostic effect of the tumor–stroma ratio in colon cancer."
ESMO open 9.4 (2024): 102988.
Plasma
Sae-Lee, Wisath, et al. " The protein organization of a red blood cell ."
Cell Reports 40.3 (2022): 111103.
Culture
Supernatants Cell Secretome Proteome Analysis
Jenull,
Sabrina, et al. "The
histone chaperone HIR maintains chromatin states to control nitrogen
assimilation and fungal virulence." Cell Reports 36.3
(2021): 109406.
Osteogenic and Fibrogenic Blood Composites
Jing, Lun, et al. "PROTEOMIC ANALYSIS IDENTIFIED LBP AND CD14 AS KEY PROTEINS IN BLOOD/BIPHASIC CALCIUM PHOSPHATE MICROPARTICLE
INTERACTIONS."
Acta Biomaterialia, (2021).
Blood
Targeted
LC-MS Proteomic Methods to Monitor and Quantify Stromal Conditioning
in Cancer from Blood Matt
Kuruc1; Swapan Roy1; Wilma Mesker2; Rob Tollenaar2; 1Biotech
Support Group LLC, Monmouth Junction, NJ; 2Leiden University
Medical Center, Leiden, Netherlands
Blood
Kuruc M, Zheng H, Sowerhardy A, Avadhani S, Roy D, et al.(2020) "New Strategies to Categorize Blood for Proteomic Biomarker Discovery."
Proteomics Bioinformatics, 2(2): 90-107.
Biotech Support Group
to exhibit at the 67th ASMS Conference on Mass Spectrometry & Allied Topics
.
Application
Report
Haiyan
Zheng
1;
Swapan Roy
2;
Devjit Roy MD
2;
Amenah Soherwardy
1;
Seema Rathman
2;
Matthew Kuruc
2 1Rutgers
Center for Integrative Proteomics, Piscataway, NJ; 2Biotech Support
Group LLC, Monmouth Junction, NJ
Stroma
Liquid Biopsy – Pan-Cancer Dysregulation of the Serum Proteome
Serum
Vialaret, Jerome & Kadi, Sarah & Tiers, Laurent & O Flynn, Robin & Lehmann, Sylvain & Hirtz, Christophe."
Albumin depletion of human serum to improve quantitative clinical proteomics.
."Current Topics in Peptide & Protein Research 19. 53-62.
Roy, Swapan, and Matthew Kuruc.
"
Methods to Monitor the Functional Subproteomes of SERPIN
Protease Inhibitors.
."Functional Proteomics. Humana Press, New York, NY, 2019. 41-54
Vialaret, Jerome, et al.
"
Albumin depletion of human serum to improve quantitative clinical proteomics.
."
Poillet-Perez, Laura, et al.
"
Autophagy maintains
tumour growth through circulating arginine.
."
Nature (2018): 1.
David
L. Wang, Chuanguang Xiao, Guofeng Fu, Xing Wang and Liang Li.
"
Identification
of potential serum biomarkers for breast cancer using a functional
proteomics technology.
."
Biomarker Research (2017) 5:11.. DOI 10.1186/s40364-017-0092-9
Sun,
Zhenyu, Xiaofeng Chen, Gan Wang, Liang Li, Guofeng Fu, Matthew Kuruc,
and Xing Wang. "
Identification
of functional metabolic biomarkers from lung cancer patient serum
using PEP technology
."
Biomarker Research 4, no. 1 (2016): 1.
Haiyan
Zheng; Caifeng Zhao; Swapan Roy; Devjit Roy MD; Amenah Soherwardy;
Ravish Amin; Matthew Kuruc. Application Report -
The
Comparison of the Serum Proteome in Individuals with Cancers versus
those without Cancer, and its application to Wellness
Dr.Swapan
Roy; Amenah Soherwardy; Ravish Amin; Matthew Kuruc.Monmouth Junction,
NJ - Application Report.
AlbuSorb™
Product Extension combines Albumin and Immunoglobulin Depletion in a
Consumable Format
Xing
Wang, Michael Davies, Swapan Roy and Matthew Kuruc.
Bead
Based Proteome Enrichment Enhances Features of the Protein Elution
Plate (PEP) for Functional Proteomic Profiling
.
Proteomes 2015, 3(4), 454-466. doi: 10.3390/proteomes3040454
Grubbs,
J. K., et al. "
Investigation
of the efficacy of albumin removal procedures on porcine serum
proteome profile1
."
(2015).
Discovery
of Functional Serum Biomarkers Using AlbuVoid™ Enrichment and
the ArrayBridge PEP Profiling Platform
.
Personal communication, Xing Wang, Ph.D., ArrayBridge (St. Louis,
MO), manuscripts in process.
Serum
Profiling Making Mark on Predictive Medicine
Vicki
Glaser.Genetic Engineering & Biotechnology News. 2011;31(7):1-55.
Kuruc
Matt.
Application
Report - AlbuVoid™ & On-Bead Digestion - Tackling the
challenges of serum proteomics (LC-MS).
Kuruc
Matt, Dr.Roy.
Application
Report - AlbuVoid™ LC-MS On-Bead – Differential
Expression of Cancer Sera Proteins Using Quantitative (iTRAQ)
Proteomics
Patents
Narain, Niven Rajin, Rangaprasad Sarangarajan, and Vivek K. Vishnudas.
"
"Interrogatory cell-
based assays for identifying drug-induced toxicity markers.
."
U.S. Patent Application No. 16/180,446.
Narain,
Niven Rajin, Rangaprasad Sarangarajan, and Vivek K. Vishnudas.
"
INTERROGATORY
CELL-BASED ASSAYS AND USES THEREOF
."
U.S. Patent No. 20,120,258,874. 11 Oct. 2012.
Plasma
Espes,
Daniel, Joey Lau, and Per-Ola Carlsson. "
Increased
circulating levels of betatrophin in individuals with long-standing
type 1 diabetes
."
Diabetologia(2013): 1-4.
Patent
- Secretome Sample Preparation
Narain,
Niven Rajin, and Paula Patricia Narain. "
COMPOSITIONS
AND METHODS FOR DIAGNOSIS AND TREATMENT OF PERVASIVE DEVELOPMENTAL
DISORDER
."
U.S. Patent No. 20,150,023,949. 22 Jan. 2015.
Narain,
Niven Rajin, Rangaprasad Sarangarajan, and Vivek K. Vishnudas.
"
INTERROGATORY
CELL-BASED ASSAYS AND USES THEREOF
."
U.S. Patent No. 20,120,258,874. 11 Oct. 2012.
Cell
Culture
Narain,
Niven Rajin, Rangaprasad Sarangarajan, Vivek K. Vishnudas, and
Michael Andrew Kiebish. "
USE
OF MARKERS IN THE IDENTIFICATION OF CARDIOTOXIC AGENTS AND IN THE
DIAGNOSIS AND MONITORING OF CARDIOMYOPATHY AND CARDIOVASCULAR
DISEASE
."
U.S. Patent 20,140,100,128, issued April 10, 2014.
On-Bead
Digestion Protocols For LC-MS Proteomic Workflows
New
on-bead digestion for LC-MS
applications
for proteomic studies
US
HUPO 2014. Frontiers in Proteomics: Advancing Biology through
Technology and Computation.
AlbuVoid™
poster, entitled "
Improved
proteomic enrichment and workflow strategies
",
poster board 089 presented at US HUPO 2014
AlbuSorb™ PLUS
Plasma samples
Grantz, Jillian M., et al.""The platelet and plasma proteome and targeted lipidome in postpartum dairy cows with elevated systemic inflammation."" Scientific Reports 14.1 (2024): 31240.
Whole blood, serum and plasma samples
DPX Technologies and Biotech Support Group Announce In-Market Partnership for High Throughput Proteomic Sample Prep
Serum/Plasma
Samples
Biotech
Support Group & Lawson Health Research
Institute Enter Collaborative Research Agreement to Monitor Protease
Inhibitor Function During Covid-19 Infections
Serum
Thangavelu,
Bharani, et al. "Dataset
of Rat and Human Serum Proteomes Derived from Differential Depletion
Strategies prior to Mass Spectrometry." Data in Brief
(2020): 105657.
Application
Report
AlbuVoid™ PLUS & AlbuSorb™ PLUS - Evaluating Different Windows of Observation Solves The Many Challenges of Serum Proteomics
AlbuSorb™
Product Extension combines Albumin and Immunoglobulin Depletion in a
Consumable Format
AlbuVoid™
PLUS - Albumin and IgG Depletion From Serum/Plasma for Proteomics
References
AlbuVoid™ PLUS & AlbuSorb™ PLUS - Evaluating Different Windows of Observation Solves The Many Challenges of Serum Proteomics
Zheng
H, Soherwardy A, Roy S, Kuruc M, Avadhani S. AlbuVoid™
Enrichment & Antibody Depletion – Tackling
the Challenges of Serum Proteomics Part II. Poster reprint first
presented at 26th International Molecular Med TRI-CON,
March
10-15, 2019, San Francisco, CA USA
Vialaret,
Jerome & Kadi, Sarah & Tiers, Laurent & O Flynn, Robin &
Lehmann, Sylvain & Hirtz, Christophe. (2018). Albumin
depletion of human serum to improve quantitative clinical proteomics.
Current
Topics in Peptide & Protein Research 19. 53-62.
Poillet-Perez,
Laura, et al. "Autophagy
maintains tumour growth through circulating arginine."
Nature
(2018): 1.
Roy,
Swapan, and Matthew Kuruc. "Methods
to Monitor the Functional Subproteomes of SERPIN Protease
Inhibitors."
Functional Proteomics. Humana Press, New York, NY, 2019. 41-54.
Mihara,
Keisuke, et al. "Identification
of Specific Protein Markers of Rheumatoid Arthritis in Synovial Fluid
and Serum."
Journal of Hard Tissue Biology 27.1 (2018): 55-58.
David
L. Wang, Chuanguang Xiao, Guofeng Fu, Xing Wang and Liang
Li. Identification
of potential serum biomarkers for breast cancer using a functional
proteomics technology.
Biomarker
Research (2017) 5:11. DOI 10.1186/s40364-017-0092-9
Zheng,
H., et al. "AlbuVoid™
coupled to on-bead digestion-tackling the challenges of serum
proteomics."
J
Proteom Bioinformatics 8.9 (2015): 225.
Zheng,
H., et al. Poster reprint first presented at 14th Human Proteome
Organization World Congress (HUPO 2015), held on September 27 –
30, 2015 entitled “New
Proteomic Workflows Combine Albumin Depletion and On Bead Digestion,
for Quantitative Cancer Serum”.
AlbuVoid™
LC-MS On-Bead For Serum Proteomics
Serum
Haiyan
Zheng, Caifeng Zhao, Meiqian Qian, Swapan Roy, Absari Arpa, Amenah
Soherwardy and Matthew Kuruc. AlbuVoid™
Coupled to On-Bead Digestion - Tackling the Challenges of Serum
Proteomics. J
Proteomics Bioinform 2015, 8:9.
Grubbs,
J. K., et al. " Investigation
of the efficacy of albumin removal procedures on porcine serum
proteome profile1."
(2015).
Discovery
of Functional Serum Biomarkers Using AlbuVoid™ Enrichment and
the ArrayBridge PEP Profiling Platform.Personal
communication, Xing Wang, Ph.D., ArrayBridge (St. Louis, MO),
manuscripts in process.
Serum
Profiling Making Mark on Predictive Medicine Vicki
Glaser.Genetic Engineering & Biotechnology News. 2011;31(7):1-55.
Kuruc
Matt, Dr.Roy. Application Report - AlbuVoid™
LC-MS On-Bead – Differential Expression of Cancer Sera Proteins
Using Quantitative (iTRAQ) Proteomics
Plasma Espes,
Daniel, Joey Lau, and Per-Ola Carlsson. "Increased
circulating levels of betatrophin in individuals with long-standing
type 1 diabetes."
Diabetologia(2013):
1-4.
Patent
- Secretome Sample Preparation Narain,
Niven Rajin, and Paula Patricia Narain. "COMPOSITIONS
AND METHODS FOR DIAGNOSIS AND TREATMENT OF PERVASIVE DEVELOPMENTAL
DISORDER."
U.S.
Patent No. 20,150,023,949. 22 Jan. 2015.
Narain,
Niven Rajin, Rangaprasad Sarangarajan, and Vivek K. Vishnudas.
" INTERROGATORY
CELL-BASED ASSAYS AND USES THEREOF."
U.S. Patent No. 20,120,258,874. 11 Oct. 2012.
Cell
Culture Narain,
Niven Rajin, Rangaprasad Sarangarajan, Vivek K. Vishnudas, and
Michael Andrew Kiebish.
"USE
OF MARKERS IN THE IDENTIFICATION OF CARDIOTOXIC AGENTS AND IN THE
DIAGNOSIS AND MONITORING OF CARDIOMYOPATHY AND CARDIOVASCULAR
DISEASE."
U.S. Patent 20,140,100,128, issued April 10, 2014.
On-Bead
Digestion Protocols For LC-MS Proteomic Workflows New
on-bead digestion for LC-MS applications for proteomic studies
US
HUPO 2014. Frontiers in Proteomics: Advancing Biology through
Technology and Computation.
AlbuVoid™ abstract
entitled "Improved
proteomic enrichment and workflow strategies",
poster
board 089 presented at US HUPO 2014
AlbuTrial™
PLUS Kit
Hemoglobin Depletion
NuGel-HemogloBind™ - Hemoglobin Capture Reagent From Blood and Hemolyzed Serum
Tumor Interstitial Fluid
Zhang, X., Li, S., Malik, I. et al. "Reprogramming tumour-associated macrophages to outcompete cancer cells."
Nature (2023).
Whole blood, serum and plasma samples
DPX Technologies and Biotech Support Group Announce In-Market Partnership for High Throughput Proteomic Sample Prep
Whole blood
Leitner, Dominique F., et al."Metabolomic, Proteomic, and Transcriptomic Changes in Adults with Epilepsy on Modified Atkins Diet."
Epilepsia (2023).
HemogloBind™ - Hemoglobin
Depletion From Hemolyzed Serum/Plasma
Fresh frozen human EDTA-whole Blood
de Boni, Laura, et al. "Aggregation-resistant alpha-synuclein tetramers are reduced in the blood of Parkinson’s patients."
EMBO Molecular Medicine (2024): 1-18.
EDTA Whole Blood (EWB)
Das, Amaresh, et al."Enhanced Recovery and Detection of Highly Infectious Animal Disease Viruses by Virus Capture Using Nanotrap® Microbiome a Particles."
(2024).
Hemolyzed Samples
Neil Adrian P. Ondevilla, Peng-Wen Liu, Wan-Ting Huang, Tzu-Ping Weng, Nan-Yao Lee, Syu-Cing Ma, Jian-Jang Huang, Tak-Wah Wong, Hsien-Chang Chang,"A point-of-care electrochemical biosensor for the rapid and sensitive detection of biomarkers in murine models with LPS-induced sepsis"
Biosensors and Bioelectronics, Volume 254, 2024, 116202, ISSN 0956-5663,
Pooled Blood Samples
Igoh, Akihisa, Masanobu Miura, and Satoru Miyaishi."Animal Species and Blood Identification with Peptide Mass Fingerprinting."
Analytical Chemistry (2024).
RBC lysates
Chen, Yaozhen, et al."Noncanonical NLRP3 Inflammasome Activation Elicits the Programmed Death of Red Blood Cells."
Available at SSRN 4626203.
Abdominal Aneurysm Samples
Jara, Zaira Palomino, et al."Distinct Mechanisms of β-Arrestin–Biased Agonist and Blocker of AT1R in Preventing Aortic Aneurysm and Associated Mortality."
Hypertension 80.2 (2023): 385-402.
Peripheral blood mononuclear cell (PBMC) whole cell lysate samples
Kaneko, Tomonori, et al."Kinome and phosphoproteome reprogramming underlies the aberrant immune responses in critically ill COVID-19 patients."
(2023).
Red blood cells
Barakat, Amey, et al."Effects of 2,3-DPG knockout on SCD phenotype in Townes SCD model mice"
American Journal of Hematology (2023).
Mouse Red Blood Cells
Zhan, Jing, et al."Silica nanoparticles trigger phosphatidylserine exposure in red blood cells and induce thrombosis risk."
Environmental Pollution (2023): 121591.
Hemolysate
Dasauni, Pushpanjali, et al."Optimization and Identification of Single Mutation in Hemoglobin Variants with 2, 2, 2 Trifluoroethanol Modified Digestion Method and Nano− LC Coupled MALDI MS/MS."
Molecules 27.19 (2022): 6357.
Whole Blood Sample
Witchey, Shannah K., et al. ""Reproductive and developmental toxicity following exposure to organophosphate ester flame retardants and plasticizers, triphenyl phosphate and isopropylated phenyl phosphate, in Sprague Dawley rats.""
Toxicological Sciences (2022).
Hemolysate Preparations Remnant White Ghosts
Sae-Lee, Wisath, et al. " The protein organization of a red blood cell ." Cell Reports
40.3 (2022): 111103.
Plasma Samples
Phillippi, Danielle T., et al. "Inhaled diesel exhaust particles result in microbiome-related systemic inflammation and altered cardiovascular disease biomarkers in C57Bl/6 male mice." Particle and fibre toxicology 19.1 (2022): 1-29.
Human serum
High-throughput, Automated INTip™ SPE Combined with AlbuSorb™ Products for Efficient Albumin and Albumin/IgG Depletion
Matthew Fitts 1; William E. Kemnitzer 1; Paul Meeh 1; Matt Kuruc 2; Swapan Roy 2; Sowmya Avadhani 2
1DPX Technologies, Columbia, SC; 2Biotech Support Group LLC, Monmouth Junction, NJ Corresponding Author: mkuruc@biotechsupportgroup.com
Urine
Samples
Juriasingani,
Smriti, et al. "Evaluating
the Effects of Subnormothermic Perfusion with AP39 in a Novel
Blood-Free Model of Ex Vivo Kidney Preservation and
Reperfusion." International
Journal of Molecular Sciences 22.13
(2021): 7180.
Lysed
RBCs
D'Alessandro,
Angelo, et al. "Hematologic
and systemic metabolic alterations due to Mediterranean type II G6PD
deficiency in a novel murine model." bioRxiv (2021).
Hemolyzed
Red Blood Cells Biological Fluids
Heather
E. McKiernan, Phillip B. Danielson, Catherine O. Brown, Masha
Signaevsky, Christian G. Westring and Kevin M. Legg, Developmental
Validation of a Multiplex Proteomic Assay for the Identification of
Forensically Relevant Biological Fluids, Forensic Science
International, (2021)
Peripheral blood derived mononuclear cells whole
cell lysate samples
Kaneko, Tomonori, et
al."System-wide hematopoietic and immune signaling aberrations in COVID-19 revealed by deep proteome and phosphoproteome analysis."
Research Square preprint (2021).
Blood cell
lysates
Yamagishi, Yoshikazu, Hirotaro Iwase, and Yasumitsu
Ogra."Post-Mortem Changes of Methomyl in Blood with Hemoglobin."
Chemical Research in Toxicology.
Reticulocytes (Retics)
lysates
Hojo-Souza NS, de Azevedo PO, de Castro JT, Teixeira-
Carvalho A, Lieberman J, et al "Contributions of IFN-γ and granulysin to the clearance of Plasmodium yoelii blood stage."
PLOS Pathogens 16(9): e1008840.
Blood
Southwell,
Rebecca Marie, Kenneth Sherlock, and Matthew Baylis. "Cross-sectional
study of British wild deer for evidence of Schmallenberg virus
infection."
Veterinary Record (2020).
Application
Reports
Hemoglobin
Removal Whitepaper Describes a Range of Depletion Strategies and
Their Successful Uses
“Hemoglobin
Removal - The Gold Standard Products”,
April 28, 2020
ebook
Describes the Role of the Innate Immunity Proteome As a Central
Modulator of Disease from Pandemic Infections to
Cancer “Categorization
of Blood Based Biomarkers – Unleashing the Power of Proteomics
To Better Understand the Innate Immune Response to Infectious and
Non-infectious Inflammatory Stimuli”,
April 17, 2020
Host red blood cells
Dziekan, Jerzy Michal, et al.
"Cellular thermal shift assay for the identification of
drug–target interactions in the Plasmodium falciparum proteome."
Nature Protocols(2020): 1-41.
Hemolyzed Serum
Craig, J. R., et al.
"A comparison of the anatomical and gastrointestinal functional development between gilt and sow progeny around birth and weaning."
Journal of animal science (2019).
Reticulocytes
Nguyen, Anthony T., et al.
"UBE2O remodels the proteome during
terminal erythroid differentiation."
Science 357.6350 (2017): eaan0218.
Perfusates
Laing, Richard W., et al.
"The use of an acellular oxygen carrier in
a human liver model of normothermic machine perfusion."
Transplantation 101.11 (2017): 2746.
Hemocyte fractions
O’Connell, Grant C., et al.
"Monocyte-lymphocyte cross-communication via soluble
CD163 directly links innate immune system activation and adaptive immune system suppression following ischemic stroke."
Scientific reports 7.1 (2017): 12940.
Hemolysate
Dasauni, Pushpanjali, et al.
"Refractive index of blood is a potential qualitative
indicator of hemoglobin disorder in humans."
Journal of Proteins & Proteomics 9.3 (2018).
Cell Lysates Of
Reticulocytes
Junqueira, Caroline, et al.
"Cytotoxic CD8+ T cells recognize and kill Plasmodium
vivax–infected reticulocytes."
Nature medicine (2018): 1.
Whole Blood Aliquots
Pácal, Lukáš, et al.
"Deleterious Effect of Advanced CKD on Glyoxalase System
Activity not Limited to Diabetes Aetiology."
.
International Journal of Molecular Sciences 19.5 (2018): 1517.
Bronchoalveolar
lavage fluid (BALF)
Maneesh
Bhargava, Kevin J. Viken, Sanjoy Dey, Michael S. Steinbach, Baolin
Wu, Pratik D. Jagtap, LeeAnn Higgins, Angela Panoskaltsis-Mortari,
Daniel J. Weisdorf, Vipin Kumar, Mukta Arora, Peter B. Bitterman,
David H. Ingbar, Chris H. Wendt.
Proteome
Profiling in Lung Injury after Hematopoietic Stem Cell
Transplantation
.
Biology of Blood and Marrow Transplantation 22 (2016)
1383-1390.
Cell
Lines
Phanse,
Sadhna, Cuihong Wan, Blake Borgeson, Fan Tu, Kevin Drew, Greg Clark,
Xuejian Xiong et al. "
Proteome-wide
dataset supporting the study of ancient metazoan macromolecular
complexes
." Data
in brief
6
(2016): 715-721.
Dried
Blood Spot(DBS)/Whole Blood
Hakuna,
Lovemore, et al.
" A
simple assay for glutathione in whole blood
."Analyst (2015).
Whole
Blood
Chalásová,
Katarína, et al.
"Transketolase
Activity but not Thiamine Membrane Transport Change in Response to
Hyperglycaemia and Kidney Dysfunction
."
Experimental and Clinical Endocrinology & Diabetes
(2017).
Chalásová, Katarína. Functional
analysis of genetic variants in genes associated with the development
of glycotoxic damage
.
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“Hemoglobin
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April 28, 2020
ebook
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HemoVoid™
Blood Card Kit The HemoVoid™ Blood Card kit
substantially reduces hemoglobin interference from dried blood spot
protein analytes
Red
Blood Cells
Dried
blood spots for detection of autologous blood doping with targeted
LC-MS/MS Matt
Kuruc1; Swapan Roy1; Johan Jakobsson2; Raik Wagner2; Christer
Malm2; 1Biotech Support Group (BSG) LLC, Monmouth Junction,
NJ; 2Pro Test Diagnostics AB (PTD), Umeå, Sweden
HemogloBind™
Blood Card Kit Hemoglobin Depletion and Protein
Enrichment From Dried Blood Spots
Red
Blood Cells
Dried
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LC-MS/MS Matt
Kuruc1; Swapan Roy1; Johan Jakobsson2; Raik Wagner2; Christer
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For
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LC-MS On-Bead
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Commonality of the Cancer Serum Proteome Phenotype as analyzed by
LC-MS/MS, and Its Application to Monitor Dysregulated Wellness
Haiyan
Zheng1; Caifeng Zhao1; Swapan Roy2; Devjit Roy MD; Amenah
Soherwardy2; Ravish Amin2; Matthew Kuruc21Rutgers Center for
Integrative Proteomics, Piscataway, NJ; 2Biotech Support Group LLC,
Monmouth Junction, NJ.
Variant
sub-populations (also known as proteoforms) of a common blood protein
– Alpha-1-Antitrypsin, with functional reporting features
severely distinguishable between cancer patients and normal/healthy
individuals. A measurable serum cancer profile that can be modeled
with categorical biomarker proteins taken from inflammation, blood
coagulation, tissue remodeling, and glycolysis, as well as new
markers of unknown function.
Cancer
Biomarker And Wellness Protein Discovery Application Report
Haiyan
Zheng1; Caifeng Zhao1; Swapan Roy2; Devjit Roy MD; Amenah
Soherwardy2; Ravish Amin2; Matthew Kuruc2 1Rutgers Center for
Integrative Proteomics, Piscataway, NJ; 2Biotech Support Group LLC,
Monmouth Junction, NJ. Application Report -
The
Comparison of the Serum Proteome in Individuals with Cancers versus
those without Cancer, and its application to Wellness
Biomarker
discovery from genomic analysis of singlular biomarkers or protein
panels can be enhanced by doing albumin depletion experiments and on
bead digestion. A wellness proteome strategy of over 200 spectrally
quantified proteins from healthy/normal or disease cancerous sera of
pancreatic, breast, lung patients are obtained. Individuals from
pancreatic, breast and lung cancer sera are analyzed by adding a
binding buffer. The bead retains serum proteome and albumin is
depleted. Subsequently the serum proteins on bead are analyzed by
wash, reduction, alkylation, trypsin digestion and are labelled.
Spectra from liquid chromatography mass spectrometry (LC-MS/MS) runs
and proteins analyzed by Xtandem with protein filters are obtained.
An example of a protein is the SERPIN family protease inhibitor. It
allows validating quantitative proteomics data, discovering newly
annotated serum proteome.
Zheng
et al. AlbuVoid™
Coupled to On-Bead Digestion - Tackling the Challenges of Serum
Proteomics.
J Proteomics Bioinform 2015, 8:9
For
cancer research, serum and plasma are especially attractive sample
types as collection of blood is common, simple and only minimally
invasive. Yet serum samples can offer unique challenges in LC-MS
proteomic analyses. The two biggest challenges being: 1) the high
abundance of Albumin accounting for about 50% of the total protein
mass and, 2) proteolytic resistance, in large part due to substantial
amount of glycoprotein, a modification that manifests proteolytic
resistance. In this short report, we describe new methods using a
surface/bead based product, AlbuVoid™, which depletes Albumin
through a negative selection or voidance strategy, retaining the vast
amount of the remaining serum proteome on the bead. We then combine
this novel enrichment, with a direct and seamless integration with
Trypsin digestion, a method conventionally referred to as on-bead
digestion. We evaluated the digestion time as a parameter to identify
whether different sub-populations of peptides and
proteins can be observed by LC-MS analyses. Using 2 different
allotted digestion times - 4 hours, and overnight, each with a
singular 3 hour gradient LC-MS run, between 400-500 total proteins
were observed for both human and rat sera, with overlapping and
distinct sub-populations observable at each digest time. These
results support that the described methods gain efficiencies over
other high abundance depletion and in-solution digestion workflows.
We solicit that such workflows will minimize many of the
inconsistencies of proteolytic hydrolysis for both discovery and
quantitative serum proteomic applications.
For
HemoVoid™ LC-MS On-Bead
HemoVoid™
LC-MS On-Bead Digest Application Report
The
data shows a comparison of Trypsin digestion of the HemoVoid™
bead-bound
sub-proteome compared a more conventional solution digest.
For
HemogloBind™
C
Wan, B Borgeson, S Phanse, F Tu, K Drew, G Clark, et al. Panorama
of ancient metazoan macromolecular complexes.
Nature Volume:525, Pages:339–344 Date published:(17 September
2015). doi:10.1038/nature14877
Two
of BSG products, NRicher™ 6 and HemogloBind™, were able
to contribute to this rigorous examination of protein complexes. When
our products were used as a pretreatment step in the overall
workflow, about twice the number of observations and annotations
became possible. This further validates that the sub-proteome bias
characteristics of NRicher™ 6 can simplify complex proteomes
into less complex sub-proteomes with efficiencies suitable for deep
functional proteome characterization. Furthermore, this study
demonstrated the importance of a key feature implicit to all of our
products; that is the maintenance of functional and structural
integrity after separations. Without that particular feature, these
additional observations would not have been possible.
Maneesh
Bhargava, Kevin J. Viken, Sanjoy Dey, Michael S. Steinbach, Baolin
Wu, Pratik D. Jagtap, LeeAnn Higgins, Angela Panoskaltsis-Mortari,
Daniel J. Weisdorf, Vipin Kumar, Mukta Arora, Peter B. Bitterman,
David H. Ingbar, Chris H. Wendt. Proteome
Profiling in Lung Injury after Hematopoietic Stem Cell
Transplantation.
Biology of Blood and Marrow Transplantation 22 (2016) 1383-1390.
The
authors consider pulmonary complications due to infection and
idiopathic pneumonia syndrome (IPS) in hematopoietic stem cell
transplant (HSCT) recipients. For this, a proteomic characterization
of global bronchoalveolar lavage fluid (BALF) was studied to identify
proteins and pathways that differentiate IPS from infectious lung
injury after HSCT. Because the BALF samples appeared tinged with
blood, the authors tested HemogloBind™ to determine whether the
removal of hemoglobin (in addition to high-abundance proteins) would
improve the depth of coverage. The article states “Hemoglobin
removal improved protein identification to 845 proteins at 1% global
FDR compared with 496 proteins with high-abundance protein depletion
alone”. The authors conclude that the protein expression
differences provide insights into mechanisms activated in lung injury
and suggest potential therapeutic targets to augment lung repair.
Alvarez-Llamas,
G., de la Cuesta, F., Barderas, M. G., Darde, V. M., Zubiri, I.,
Caramelo, C., Vivanco, F. A
novel methodology for the analysis of membrane and cytosolic
sub-proteomes of erythrocytes by 2-DE.
Electrophoresis.2009;30:4095-4108
Authors
in this study focused on the analysis of human cytosolic and membrane
sub-proteomes. Hemoglobin from samples of red blood cells was studied
using different strategies for isolation of the membrane and
cytosolic fractions to determine the influence it has on proteome
profiling by 2-DE and hemoglobin removal. Biotech Support Group's
hemoglobin depletion reagent, HemogloBind™ was successfully
used to erythrocyte cells. The results showed that Hemoglobind™
does have a high degree of specificity for hemoglobin and minimal
interference. Particularly interesting is how authors developed a
novel combined strategy based on hypotonic lysis isolation for
identification of high molecular weight proteins (i.e. spectrin,
ankyrin) by nano-LC coupled to an LTQ-Orbitrap mass spectrometer.
For
Cleanascite™
Waldron,
Richard T., et al. "Ethanol
Induced Disordering of Pancreatic Acinar Cell Endoplasmic Reticulum:
an ER Stress/Defective Unfolded Protein Response Model."
Cellular and Molecular Gastroenterology and Hepatology(2018).
The
authors’ investigated the association of heavy alcohol
consumption with pancreas damage, with consideration of light
drinking that shows the opposite effects, reinforcing proteostasis
through the unfolded protein response orchestrated by X-box binding
protein 1. The article states that the endoplasmic reticulum “RER
fractions (100 mg) were extracted by shaking for 15 minutes at 37°C
in buffer comprising 100 mmol/L Tris pH 7.0, containing 25%
acetonitrile, 0.1% sodium dodecyl sulfate, and 0.05% sodium
deoxycholate (Buffer B), in 1.5 mL Eppendorf Protein LoBind tubes
flushed of air using N2 gas. Next, 75 mL of a 1:1 slurry of
Cleanascite delipidizing beads were added, and the tubes were flushed
with N2 gas and rotated end-over-end for 15 minutes at room
temperature. Slurries were spun at 10,000 rpm for 5 minutes at room
temperature, clarified extracts were transferred to clean tubes, and
pelleted beads were discarded.” The isolated ER proteome was
then analyzed by OXICAT LC-MS. The study concludes that
ethanol-induced changes in endoplasmic reticulum protein redox and
structure/function emerge from an unfolded protein response–deficient
genetic model.
Taylor,
Steven W., Nigel J. Clarke, Zhaohui Chen, and Michael J. McPhaul. "A
high-throughput mass spectrometry assay to simultaneously measure
intact insulin and C-peptide."
Clinica Chimica Acta 455 (2016): 202-208.
In
brief, the article’s authors aimed at simultaneously measuring
intact insulin and proinsulin derived C-peptide, to help predict
development of diabetes mellitus, as well as in differential
diagnosis in cases of hypoglycemia. The article states “…15
µl of internal standard were added to each well followed by 50
µl of Cleanascite™ delipidation reagent previously mixed
into a uniform suspension by a brief aspiration/dispense cycle within
its reagent reservoir.” The article further notes a key
component of the methodology as “…the use of a
delipidation reagent to enhance immunocapture…The result was
greatly enhanced recoveries and tighter CVs for the IS {internal
standard} throughout the
plate”.
Megger,
Dominik A., et al. "One
Sample, One Shot-Evaluation of sample preparation protocols for the
mass spectrometric proteome analysis of human bile fluid without
extensive fractionation."
Journal of Proteomics (2016).
In
brief, the article’s authors report methods to overcome the
biological variability of analyzing a high number of bile samples.
They advance that easy sample preparation protocols are demanded
representing a compromise between proteome coverage and simplicity in
this study. For this, they evaluated the performance of simple
workflows allowing for "one sample, one shot" experiments
to identify biomarker candidates for various diseases of the
hepatobiliary system. In detail, sixteen different protocols with
modifications at the stages of desalting, delipidation,
deglycosylation and tryptic digestion were examined. The article
states “For delipidation, the Cleanascite™ Lipid Removal
Reagent and Clarification Kit (BSG, NJ 08852, USA) was used following
manufacturer's instructions.”. The authors concluded that
delipidation yielded a considerable number of complementary protein
identifications and that Cleanascite™ treatment was
indispensable for in-solution digestion methods.
Laohaviroj,
Marut, et al. "A comparative proteomic analysis of bile for
biomarkers of cholangiocarcinoma." Tumor
Biology
39.6 (2017): 1010428317705764.
http://journals.sagepub.com/doi/abs/10.1177/1010428317705764
The
article’s authors used a quantitative proteomics approach to
identify potential tumor-associated proteins in the bile fluid of six
cholangiocarcinoma patients. Cholangiocarcinoma is a primary
malignant tumor of the bile duct epithelium and is usually detected
at an advanced stage when successful treatment is no longer possible.
As the tumor originates from the bile duct epithelium, bile is an
ideal source of tumor biomarkers for cholangiocarcinoma. In this
study, Isobaric labeling, coupled with Tandem mass spectrometry, was
used to quantify protein levels in the bile of cholangiocarcinoma and
control patients. The article states “Cleanascite™
(Biotech Support Group, USA), lipid removal reagent, was added to the
bile and the sample was vertically shaken for 1 h at 4°C before
centrifugation at 10,000 × g
for
1 min.”. The authors concluded that in all, 63 proteins were
significantly increased in cholangiocarcinoma bile compared to normal
bile. Alpha-1-antitrypsin was one of the overexpressed proteins that
increased in cholangiocarcinoma bile samples. Fecal enzyme-linked
immunosorbent assay showed that alpha-1-antitrypsin level was able to
distinguish cholangiocarcinoma patients from normal individuals,
thereby making Alpha-1-antitrypsin a potential marker for early
diagnosis of cholangiocarcinoma.
Farina
A, Dumonceau JM, Frossard JL. Proteomic
Analysis of Human Bile from Malignant Biliary Stenosis Induced by
Pancreatic Cancer Journal
of Proteome Research.2009; 8(1):159-69
Using
Cleanascite™ scientists isolated and identified hydrophobic
polypeptides in human bile and subsequently performed specialized
reversed-phase chromatography and gel-filtration, and MALDI-TOF mass
spectrometry, to identify a small subset of five proteins. Bile fluid
was obtained by endoscopic retrograde cholangiopancreatography (ERCP)
from a patient with cholangiocarcinoma. Unfractionated bile fluid was
centrifuged and partially cleared supernatant was then mixed with 250
μl of Cleanascite™ followed by rotation, centrifuged, clear
away the formed lipid-micelles.
Kristiansen
TZ, Bunkenborg J, Gronborg M et al A
Proteomic Analysis of Human Bile Molecular
and Cellular Proteomics.2004;3:715-728
Researchers
discovered large amounts of lipids, bile salts in bile fluid obtained
by ERCP from patients with cholangiocarcinoma. To identify proteins
in bile fractions researchers used Cleanascite™ to precipitate
lipids from “unfractionated bile” followed by
one-dimensional gel electrophoresis, lectin affinity chromatography
and liquid chromatography tandem mass spectrometry.
For
NRicher™ 6
C
Wan, B Borgeson, S Phanse, F Tu, K Drew, G Clark, et al. Panorama
of ancient metazoan macromolecular complexes.
Nature Volume:525, Pages:339–344 Date published:(17 September
2015).
doi:10.1038/nature14877
Two
of BSG products, NRicher™ 6 and HemogloBind™, were able
to contribute to this rigorous examination of protein complexes. When
our products were used as a pretreatment step in the overall
workflow, about twice the number of observations and annotations
became possible. This further validates that the sub-proteome bias
characteristics of NRicher™ 6 can simplify complex proteomes
into less complex sub-proteomes with efficiencies suitable for deep
functional proteome characterization. Furthermore, this study
demonstrated the importance of a key feature implicit to all of our
products; that is the maintenance of functional and structural
integrity after separations. Without that particular feature, these
additional observations would not have been possible. (Note
– NRicher™ was referred to by a earlier name, Prospector™
in the article)
For
NRicher™ Mx
Poster
reprint from US HUPO 2014 Conference, April 6-8, 2014. Improved
proteomic and enrichment strategies
Three
common goals prior to LC-MS are:
1.
To enrich specialized sub-proteomics or alternatively - deplete high
abundance protein(s)
2.
Get efficient and consistent trypsin digestion
3.
Streamline workflows to minimize handling, potential for variance and
decreased costs.
To
assist in all 3 aspects at once, we have developed a platform surface
chemistry with derivative products to support different applications.
The surface chemistry platform called NuGel™,
is based on porous silica, a chromatography industry standard and an
advantageous matrix suitable for proteome separations. With NuGel™,
non-specific sites have been virtually eliminated making it an ideal
support for proteome enrichment. While many methods claim to reduce
the dynamic range of protein concentrations within complex mixtures,
NRicher™
Mx is
the only one that is universal as it can be applied to any tissue
from any biological source, and is suitable for small sample and
protein loads; only about 1 mg total protein being required.
Protein
Enrichment
BSG Highlights from US HUPO 2024 and MSACL 2024
"NRicher™ : Family Specific Enrichment For Targeted Proteomics"
Abstract The need for new biomarkers to support personalized healthcare, has fostered numerous proteomic innovations. Still, a number of challenges remain. One is the preponderance of high abundance proteins and, concurrently in targeted proteomic workflows, efficiency and consistency in quantifying target peptides from different sample cohorts. This is in part due to the changing landscape of proteins/peptides not associated with the selected targets. A solution for both these challenges is now available through a suite of products called NRicher™. This bead-based technology is derived from experience of over 10 years at the forefront of manufacturing beads (i.e., ionic, hydrophobic, hydrogen bonding, aromatic, polymeric) with differential proteome binding properties. NRicher™ consists of consumable chemically derived porous beads, and an adaptability to bead cocktails, even with seemingly incompatible surface features; an important distinction of porous, over non-porous magnetic beads. NRicher™ products do not require any specialized instruments, can be processed using a standard microfuge, with adaptability to automated liquid handlers.
Highlights
• After NRicher , target peptides have enriched spectral signal, even as gradient times are reduced
• NRicher sub-proteome enrichment can minimize acquisition time, collectively improving overall throughput, cost, and productivity
• Investigate out of the Venn Diagram box. Specific target peptides that report functional and variant regions promise actionable insights and potential multiplex biomarkers for disease.
Xing
Wang, Michael Davies, Swapan Roy and Matthew Kuruc.
Bead
Based Proteome Enrichment Enhances Features of the Protein Elution
Plate (PEP) for Functional Proteomic Profiling
. Proteomes
2015, 3(4),
454-466 doi: 10.3390/proteomes3040454
Saliva
Gutiérrez,
Ana, et al. "
Influence
of different sample preparation strategies on the proteomic
identification of stress biomarkers in porcine saliva.
"
BMC Veterinary Research 13.1 (2017): 375.
Gutiérrez,
A. M., et al. "
Detection
and first characterization of an uncommon haptoglobin in porcine
saliva of pigs with rectal prolapse by using boronic acid sample
enrichment
."
animal 11.5 (2017): 845-853.
Toxoplasma gondii
Swapna LS, Stevens GC, Sardinha-Silva A, Hu LZ, Brand V, Fusca DD, et al."ToxoNet: A high confidence map of protein-protein interactions in Toxoplasma gondii." PLoS Comput Biol 20(6): e1012208. https://doi.org/10.1371/ journal.pcbi.1012208
Toxoplasma gondii
Swapna LS, Stevens GC, Sardinha-Silva A, Hu LZ, Brand V, Fusca DD, et al."ToxoNet: A high confidence map of protein-protein interactions in Toxoplasma gondii." PLoS Comput Biol 20(6): e1012208. https://doi.org/10.1371/ journal.pcbi.1012208
Toxoplasma gondii
Swapna LS, Stevens GC, Sardinha-Silva A, Hu LZ, Brand V, Fusca DD, et al."ToxoNet: A high confidence map of protein-protein interactions in Toxoplasma gondii." PLoS Comput Biol 20(6): e1012208. https://doi.org/10.1371/ journal.pcbi.1012208
Toxoplasma gondii
Swapna LS, Stevens GC, Sardinha-Silva A, Hu LZ, Brand V, Fusca DD, et al."ToxoNet: A high confidence map of protein-protein interactions in Toxoplasma gondii." PLoS Comput Biol 20(6): e1012208. https://doi.org/10.1371/ journal.pcbi.1012208
Virus Enrichment
Patents
Parthasarathy,
Ranjani V., Hsi-Chou Liu, Wensheng Xia, Assumpta Bennaars-Eiden, Paul
N. Holt, William Bedingham, Christopher R. Kokaisel, and Jeffrey C.
Pederson. "
Methods
for nucleic acid amplification
."
U.S. Patent Application 12/596,346, filed April 25, 2008.
Bedingham,
William, Barry Robole, Ranjani Parthasarathy, and Katya Ericson.
"Variable Valve Apparatus and Methods." U.S. Patent
Application 11/684,656, filed March 12, 2007.
Journal
Citations
Cell Culture Supernatant Fluids
Dengue
Virus
Food
Samples
Maurer,
John, ed.
PCR
methods in foods
.
Springer
Science & Business Media, 2006.
Sair,
A. I., D. H. D'souza, and L. A. Jaykus. "
Human
enteric viruses as causes of foodborne disease
." Comprehensive
reviews in food science and food safety
1.2
(2002): 73-89.
Savers,
Screen. "
EXHIBIT
DESCRIPTIONS.
" Microbial&
Comparative Genomics
2.3
(1997): 244-249.
Food
and Water Samples
Isometric
Virus
Hantaan
Virus
Yu,
Hai-Tao, Hong Jiang, Ye Zhang, Xue-Ping Nan, Yu Li, Wei Wang, Wei
Jiang et al. "
Hantaan
virus triggers TLR4-dependent innate immune responses
."Viral
immunology
25,
no. 5 (2012): 387-393.
Human
Enteric Viruses
Human
Mouth Virus
Lepidoptera:
Gelechiidae
Serum
Abdurahman,
Samir.
Studies
on HIV-1 core assembly
.
Institutionen för laboratoriemedicin/Department of Laboratory
Medicine, 2007.
Human
Immunodeficiency Virus Type 1
Plasma
Polio
Virus
Ting,
W.T. E
.,
E. M. Nielson, and C.C. Tseng. 1997.
The
use of Viraffinity matrix to concentrate waterborne polioviruses for
RT-PCR detection
.
abstr. Q-169. p.484.
In Abstracts
of the 97th General Meeting of the American Society for Microbiology
1997, American Society for Microbiology, Washington D.C.
Bacteriophage
Lambda DNA
Hitti,
J. "Fast and Convenient Purification of Bacteriophage Lambda DNA
with Viraffinity™ Matrix, poster Cold Spring Harbor Conference
on Genome Mapping & Sequencing." (1997).
Metagenomic
Analysis of the Human Mouth Virus Population and Characterisation of
Two Lytic Viruses
Ahmed
N. Al-Jarbou, MSc University of Leicester
Functional &
Chemical Proteomics
NuGel™
NRicher™ Mx
Suggested
References
Biotech Support Group to exhibit at the 71st ASMS Conference on Mass Spectrometry and Allied Topics, June 4 - 8, 2023 in Houston, Texas
Featured at our Booth 208, will be consumable sample prep products for proteome enrichment, and on-bead digestion for rapid and streamlined workflows to improve low abundance coverage and quantification of select sub-proteomics.
The
Functional & Chemical Proteomics Handbook
03/2016
Oka,
Amita R., Matthew P. Kuruc, Ketan M. Gujarathi, and Swapan Roy.
"
Functional
Proteomic Profiling of Phosphodiesterases Using SeraFILE Separations
Platform.
" International
Journal of Proteomics
2012
(2012).
New
Chemical Proteomic Methods To Access Drug-Protein Interactions
US
HUPO 2014. Frontiers in Proteomics: Advancing Biology through
Technology and Computation.
NuGel™ PROfessor™ abstract
entitled "
Compound-
Centric
Displacement Proteomics - An Advantaged Method To Survey Small
Molecule-Protein Interactions
" poster
board 096 presented at US HUPO 2014
NuGel™
Related References
Patents
Monoclonal
antibodies directed to the cytotoxic lymphocyte maturation
factor
European
Patent EP0790255
Purification
of immunoglobulins using affinity chromatography and peptide
US
2006/0153834 A1
Affinity
Chaumet,
Alexandre, Sandrine Castella, Laïla Gasmi, Aurélie
Fradin, Gilles Clodic, Gérard Bolbach, Robert Poulhe, Philippe
Denoulet, and Jean-Christophe Larcher. "
Proteomic
analysis of Interleukin enhancer binding factor 3 (Ilf3) and Nuclear
Factor 90 (NF90) interactome.
"Biochimie
(2013).
Dermot
Walls, Robert McGrath and Sinéad T.Loughran
A
Digest of Protein Purification
. Methods
Molecular Biology.
Volume
681: 3-23 (2011)
Ehrlich,
G. K., Michel, H., Chokshi, H. P. and Malick, A. W.
Affinity
purification and characterization of an anti-PEG IgM
. Journal
of Molecular Recognition
,
22: 99–103 (2009).
Development
of hepatitis B virus capsids into a whole-chain protein antigen
display platform: New particulate Lyme disease vaccines
.International
Journal of Medical Microbiology
Volume
298, Issues 1-2, 3 January 2008, Pages 135-142
A
sensitive and high-throughput assay to detect low-abundance proteins
in serum
Hongtao
Zhang, Xin Cheng, Mark Richter & Mark I Greene.
Nature
Medicine
12,
473 - 477 (2006)
Transformation
of a L-peptide epitope into a D-peptide analog.
Peptides
Frontiers of Peptide Science American Peptide Symposia
,
2002, Volume 5, Session XI, 769-770
Expression
and folding of an antibody fragment selected in vivo for high
expression levels in Escherichia coli cytoplasm
. Research
in Microbiology
Volume
153, Issue 7, September 2002, Pages 469-474
Identification
of model peptides as affinity ligands for the purification of
humanized monoclonal antibodies by means of phage display
Journal
of Biochemical and Biophysical Methods
Volume
49, Issues 1-3.2001
George
K. Ehrlich, Pascal Bailon, Wolfgang Berthold.
Phage
Display Technology - Identification of Peptides as Model Ligands for
Affinity Chromatograph
y Affinity
Chromatography Methods in Molecular Biology
,
2000, Volume 147, 209-220
A
Digest of Protein Purification and partial amino acid sequence of a
28 kDa cyclophilin-like component of the rat liver sigma
receptor
. Life
Sciences
,
Volume 55, Issue 8, 1994.
Nachman,
M., Azad, A. R. M. and Bailon, P. (1992),
Efficient
recovery of recombinant proteins using membrane-based immunoaffinity
chromatography (MIC)
. Biotechnology
and Bioengineering
,
40: 564–571.
Kinetic
aspects of membrane-based immunoaffinity chromatography.
Journal
of Chromatography A Volume 597, Issues 1-2, 24 April 1992, Pages
167-172
Identification
of model peptides as affinity ligands for the purification of
humanized monoclonal antibodies by means of phage display
.
Methods in Molecular Biology, 2000, Volume 147, 209-220
Membrane-based
receptor affinity chromatography
.
Journal of Chromatography A Volume 597, Issues 1-2, 24 April 1992,
Pages 155-166 9th International Symposium on Affinity Chromatography
and Biological Recognition
Ion
Exchange
Levin
W Protein
Purification
of recombinant human secretory phospholipase A2 (group II) produced
in long-term immobilized cell culture
.Expr
Purif
1992
Feb;3(1):27-35.
Genomics
ProCipitate™
- Solid-phase Protein Extraction Reagent DNA Isolation / Microbial &
Proteoglycan Enrichment
Review ProCipitate™,
Superior Substitute to Phenol/Chloroform for DNA Isolation &
Protein Extraction
.
by Matt Kuruc February 23, 2015
Patents
U.S.
Patent Numbers 5,294,681, 5,453,493 and other patents pending.
U.S.
Patent Number 5,538,870,
Method
for Preparing Nucleic Acids For Analysis And Kits Useful Therefore
.
Enteric
Viruses
Richards,
Gary P., and Gail E. Greening. "
Detection
of enteric viruses in shellfish
." Molluscan
Shellfish Safety
.
Springer Netherlands, 2014. 177-183.
Schwab
KJ; De Leon R; Sobsey MD.
Immunoaffinity
concentration and purification of waterborne enteric viruses for
detection by reverse transcriptase PCR
.
Applied and Environmental Microbiology.1996;62(6):2086-94
Schwab
KJ, De Leon R, Sobsey MD
Concentration
and purification of beef extract mock eluates from water samples for
the detection of enteroviruses, hepatitis A virus, and Norwalk virus
by reverse transcription-PCR
.
Applied and Environmental Microbiology.1995; 61(2): 531-537
LA
Jaykus, R De Leon and MD Sobsey.
A
virion concentration method for detection of human enteric viruses in
oysters by PCR and oligoprobe hybridization
Applied
and Environmental Microbiology.1996; 62(6): 2074–2080
Mycobacterium
Avium Paratuberculosis
Charles
G. Thornton; Kerry M. MacLellan; Judith R. Stabel; Christine
Carothers; Robert H. Whitlock; Selvin Passen
Application
of the C18-Carboxypropylbetaine Specimen Processing Method to
Recovery of Mycobacterium avium subsp. paratuberculosis from Ruminant
Tissue Specimens
Journal
of Clinical Microbiology.2002;40:5;1783-1790
Zoltan
S.; Gyimesi; Ilse H.; Stalis; Janice M.; Miller; Charles O
Detection
of Mycobacterium avium Subspecies avium in Formalin-Fixed,
Paraffin-Embedded Tissues of Captive Exotic Birds Using Polymerase
Chain Reaction
.
Thoen Journal of Zoo and Wildlife Medicine.1999;30:3:348-353
Miller,
J.M., et al,
Polymerase
chain reaction identification of Mycobacterium avium in
formalin-fixed, paraffin-embedded animal tissues.
Journal
of veterinary diagnostic investigation.1999.11:436-440
Paraffin-embedded
tissues
Ellingson,
J. L. E., et al. "
Detection
of Mycobacterium avium subspecies paratuberculosis in free-ranging
bison (Bison bison) by PCR
." Molecular
and cellular probes
19.3
(2005): 219-225.
Recombinant
Bacterial Colonies
O.
Umesh K. Reddy; Alan E. Pepper; Ibrokhim Abdurakhmonov; Sukumar Saha;
Johnie N. Jenkins; Thomas Brooks, Yuksel Bolek; Kamal M. El-Zik
New
Dinucleotide and Trinucleotide Microsatellite Marker Resources
The
Journal of Cotton Science.2001;5:103-113
Quiniou
SM; Katagiri T; Miller NW; Wilson M; Wolters WR; Waldbieser
GC
Construction
and characterization of a BAC library from a gynogenetic channel
catfish Ictalurus punctatus
.
Genetics, selection, evolution : GSE. 2003;35(6):673-83
Bacterial
artificial chromosome (BAC) vector
J
M Kelley; C E Field; M B Craven; D Bocskai; U J Kim; S D Rounsley; M
D Adams.
High
Throughput Direct End Sequencing of BAC Clones
.
Nucleic Acids Research.1999.15;27(6):1539-1546
Carcinoma
Cell Lines & Bacterial Artificial Chromosomes (BACs)
Alsop,
Amber E., Andrew E. Teschendorff, and Paul AW Edwards. "
Distribution
of breakpoints on chromosome 18 in breast, colorectal, and pancreatic
carcinoma cell lines
." Cancer
genetics and cytogenetics
164.2
(2006): 97-109.
Plasmid
Deoxyribonucleic acid (DNA)
G.M.
Huang; K. Wang; C.L. Kuo; B. Paeper; L. Hood
A
High-Throughput Plasmid DNA Preparation Method
Analytical
Biochemtry.1994;15;223(1):35-8
Robert
R. Klein, Daryl T. Morishige, Patricia E. Klein, Jianmin Dong; John
E. Mullet.
High
Throughput BAC DNA Isolation for Physical Map Construction of
Sorghum.
Plant
Molecular Biology Reporter.1988;16(4):651-364
Deoxyribonucleic
acid (DNA)
Kozekov
ID; Turesky RJ; Alas GR; Harris CM; Harris TM; Rizzo CJ.
Formation
of Deoxyguanosine Cross-Links from Calf Thymus DNA Treated with
Acrolein and 4-Hydroxy-2-nonenal.
Chemical
Research in Toxicology.2010;23(11):1701-1713
Applied
Biosystems User Bulletin. Subject: Sequencing Large DNA Templates.
David
C. Bruce; Mark O. Mundt; Kim K. McMurry; Linda J. Meincke; Donna L.
Robinson; Norman A. Doggett; Larry L. Deaven.
BAC
Library End Sequencing in Support of Whole Genome Assemblies
DOE
Joint Genome Institute and Center for Human Genome Studies, Los
Alamos National Laboratory
Dr.
Domon, National Agricultural Research Center for Kyushu Okinawa
Region, Japan, Extraction of Rush DNA, unpublished personal
correspondence, 2004.
DNA
Extraction Genetic Diversity as an Indicator of Ecosystem Condition
and Sustainability
for
Regional Assessments of Stream Condition in the Eastern United States
Human
Fibroblasts
Stephanie
M Cohen, Terrence S Furey, Norman A Doggett, and David G
Kaufman.
Genome-wide
sequence and functional analysis of early replicating DNA in normal
human fibroblasts
BMC
Genomics.2006;7: 301
Norovirus,
Adenovirus
Roberto
A. Rodríguez, Lauren Thie, Christopher D. Gibbons, Mark D.
Sobsey.
Reducing
the effects of environmental inhibition in quantitative real-time PCR
detection of adenovirus and norovirus in recreational
seawaters.
Journal
of Virological Methods;2012:181(S1):43-50
Concentration
and purification of beef extract mock eluates from water samples for
the detection of enteroviruses, hepatitis A virus, and Norwalk virus
by reverse transcription-PCR
.
Applied and environmental microbiology.1995;61(2):531-7
Blood
Krupey,
J., et al,
100,000+
PCRs Possible from 10 ml Blood
,
poster Biotechniques Symposium, 2003.
Human
T-cell lymphotrophic virus I-induced adult T-cell leukemia (ATL)
J
D Burton; R N Bamford; C Peters; A J Grant; G Kurys; C K Goldman; J
Brennan; E Roessler; T A Waldmann.
A
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human adult T-cell leukemia line, stimulates T-cell proliferation and
the induction of lymphokine-activated killer cells
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of the National Academy of Sciences of the United States of
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Zebrafish
genomic library of bacterial artificial chromosome (BAC) clones and
BAC DNA
McDermott,
Brian M., et al.
Transgenic
labeling of hair cells in the zebrafish acousticolateralis system
.
Gene Expression Patterns 10.2 (2010): 113-118.
Featured
Applications
Featured
Application - Bilirubin Analysis
In
brief, the study evaluated the role of the a peptide inhibitor of
complement C1 (PIC1) in an animal model of acute intravascular
hemolysis in both prevention and rescue scenarios. The authors state
"To remove free Hb that may cause optical interference in
bilirubin analysis, we treated all the samples with Hb depletion from
hemolyzed serum/plasma (HemogloBind, Biotech Support Group).
Bilirubin concentration was then measured with a Bilirubin Assay Kit
(Sigma-Aldrich, St. Louis, MO)."
Featured
Application - Whole Blood
Thomas
H. Snider, Kevin G. McGarry, Michael C. Babin, David A. Jett, Gennady
E. Platoff Jr., and David T. Yeung. Acute Toxicity of Phorate Oxon by
oral gavage in the Sprague-Dawley rat.
Fundam.
Toxicol. Sci. Vol. 3, No.5, 195-204, 2016.
The
article describes studies of the oral toxicity of Phorate Oxon with
emphasis on gender and age-related effects in rats. The authors used
HemogloBind™ as part of the protocol to measure cholinesterase
activity. The article states “…80 µl aliquots of
whole blood were removed, diluted and treated with HemogloBind™
to remove hemoglobin for later assay to detect cholinesterase
activity…
Featured
Application - Macromolecular Complexes
C
Wan, B Borgeson, S Phanse, F Tu, K Drew, G Clark, et al.
Panorama
of ancient metazoan macromolecular complexes.
Nature
Volume:525, Pages:339–344 Date published:(17 September 2015).
doi:10.1038/nature14877
Two
of BSG products, NRicher™ 6 and HemogloBind™, were able
to contribute to this rigorous examination of protein complexes. When
our products were used as a pretreatment step in the overall
workflow, about twice the number of observations and annotations
became possible. This further validates that the sub-proteome bias
characteristics of NRicher™ 6 can simplify complex proteomes
into less complex sub-proteomes with efficiencies suitable for deep
functional proteome characterization. Furthermore, this study
demonstrated the importance of a key feature implicit to all of our
products; that is the maintenance of functional and structural
integrity after separations. Without that particular feature, these
additional observations would not have been possible.
Human
Peripheral Blood Mononuclear Cells (PBMCs)
Rubio-Navarro,
Alfonso, et al."
Hemoglobin
induces monocyte recruitment and CD163-macrophage polarization in
abdominal aortic aneurysm.
"International
Journal of Cardiology (2015)."
A
research article by authors Rubio-Navarro, Alfonso, et al in the
journal International Journal of Cardiology
(
http://www.internationaljournalofcardiology.com/article/S0167-5273(15)30284-9/fulltext)
cites Biotech Support Group’s HemogloBind™ sample
preparation reagent to deplete hemoglobin (Hb) from conditioned
medium from healthy aortas or abdominal aortic aneurysm. The article
states:"Conditioned mediums from AAA were incubated with
HemogloBind™ reagent for hemoglobin depletion".
In
brief, authors describe high infiltration of CD163 monocytes
surrounding micro-vesicles, low expression of CD14+ & CD16-
monocytes and high CD163 mRNA/protein expression is a feature of
abdominal aortic aneurysm (AAA) molecular pathology. Healthy aorta
conditioned medium or complete or hemoglobin-depleted conditioned
medium from abdominal aortic aneurysm were mixed with M-CSF
macrophages to track CD163 and HLA-DR expression or hemoglobin
uptake.
“We
are pleased with this data on abdominal aortic aneuryism &
hemoglobin proteomics. HemogloBind™ minimizes hemoglobin
interference from blood samples and allows research on cardiovascular
pathology” states Swapan Roy, Ph.D., President and Founder of
Biotech Support Group.
Dried
Blood Spot(DBS)/Whole Blood
Hakuna,
Lovemore, et al. "
A
simple assay for glutathione in whole blood.
"Analyst
(2015).
A
research article in the journal Analyst
(
http://pubs.rsc.org/en/content/articlelanding/2015/an/c5an00345h)
cites Biotech Support Group’s HemogloBind™ sample
preparation reagent to deplete hemoglobin (Hb) from whole blood
samples containing glutathione to minimize interference from Hb in
GSH fractions. Using a resorufin-acrylate fluorescent probe, GSH is
quantitated in deproteinzed blood plasma and whole blood samples. The
article states:
"Apart
from dilution, Hb can be removed using a commercial product,
HemogloBind™, which can isolate and remove up to 90% of blood
Hb." Glutathione (GSH) is an antioxidant involved on nitric
oxide regulation, covalent hemoglobin binding, DNA binding,
leukotriene synthesis, protein synthesis and sepsis pathways. GSH is
elevated in cancer tissues and proper minimally invasive GSH sample
preparation from dried blood samples (DBS) allows research on
neurodegenerative diseases, chronic respiratory diseases and
diabetes. Authors Lovemore, et al cite a DBS method to fractionate
GSH from blood components, deproteinization by filtration and
depletion of hemoglobin enhances quantification & identification
of GSH in whole blood samples. Then size exclusion chromatography or
fluorescence imaging detection is performed for quantitative analysis
and glutathione assay research.
Featured
Application - Virus Proteomics
Romain
Fragnoud, Marie Flamand, Frederic Reynier, Philippe Buchy, Vasna
Duong, Alexandre Pachot, Glaucia Paranhos-Baccala and Frederic Bedin.
Differential proteomic analysis of virus enriched fractions obtained
from plasma pools of patients with dengue fever or severe dengue. BMC
Infectious Diseases (2015)
15:518.
http://www.ncbi.nlm.nih.gov/pubmed/26572220
In
brief, the article’s authors report a method to compare the
proteomes of virion-enriched fractions purified from plasma pools of
patients with dengue fever or severe dengue. Virions were purified by
ultracentrifugation combined with Viraffinity™. Following
in-gel hydrolysis, peptides were analyzed by LC-MS. The article
states “A technique based on ultracentifugation (Step 1)
followed by concentration using…Viraffinity™, was
created to obtain a fraction of plasma enriched with DV particles. A
positive signal corresponding to monomeric (60 kDa) and dimeric E
protein (120 KDa) was observed in the DV-infected samples, and became
more intense after the Viraffinity™ step…Densitometry
indicated that the protein complexity of the purified samples was
reduced by roughly 350-fold compared to the unpurified samples.”.
The authors conclude that the Viraffinity™ based technique of
virion-enrichment allowed them to identify two host proteins that
have prognostic value for classifying patients with acute dengue who
are more likely to develop a severe dengue.
Featured
Application - microRNA from Egg Yolk
Ben
Wade, Michelle Cummins, Anthony Keyburn and Tamsyn M.
Crowley.
Isolation
and detection of microRNA from the egg of chickens
.
BMC Research Notes 2016 9:283. DOI: 10.1186/s13104-016-2084-5
In
brief, the article’s authors report a method for the
reproducible and reliable isolation of miRNA from the albumen and
yolk of chicken eggs. These methods will allow the investigation of
epigenetic programming in chick development previously unknown, and
how this impacts the nutritional value of eggs for human consumption.
The article states “…400 µl aliquots of the
yolk/lysis solution was dispensed into five 1.5 ml microcentrifuge
tubes. To each of these aliquots 600 µl of Cleanascite™
was added followed by rigorous vortexing until the sample became
homogenous. The Cleanascite™ removes the lipid from this high
fat tissue that would otherwise interfere with the extraction
process…"
Application
Reports
Hemoglobin
Removal Whitepaper Describes a Range of Depletion Strategies and
Their Successful Uses
“Hemoglobin
Removal - The Gold Standard Products”,
April 28, 2020
ebook
Describes the Role of the Innate Immunity Proteome As a Central
Modulator of Disease from Pandemic Infections to
Cancer “Categorization
of Blood Based Biomarkers – Unleashing the Power of Proteomics
To Better Understand the Innate Immune Response to Infectious and
Non-infectious Inflammatory Stimuli”,
April 17, 2020
Stroma
Liquid Biopsy™ - Blood-based biomarkers to monitor stromal
conditioning in cancer. Published February, 2019.
Haiyan
Zheng
(1),
Swapan Roy
(2),
Amenah Soherwardy
(1),
Seema Rahman
(2),
Matthew Kuruc
(2); (1)Rutgers
Center for Integrative Proteomics, Piscataway, NJ;
(2)Biotech
Support Group LLC, Monmouth Junction, NJ; entitled
"Stroma
Liquid Biopsy - Proteomic Profiles for Cancer Biomarkers
"
Poster
Reprint First Presented At AACR Annual Meeting 2016 Conference, Held
April 17-20, 2016 New Orleans, LA USA.
The
Commonality of the Cancer Serum Proteome Phenotype as analyzed by
LC-MS/MS, and Its Application to Monitor Dysregulated Wellness
Haiyan
Zheng
1;
Caifeng Zhao
1; Swapan
Roy
2;
Devjit Roy MD; Amenah Soherwardy
2;
Ravish Amin
2;Matthew
Kuruc
21Rutgers
Center for Integrative Proteomics, Piscataway, NJ;
2Biotech
Support Group LLC, Monmouth Junction, NJ
The
Functional Subproteomes of SERPIN Protease Inhibitors Are Now Open
For LC-MS Biomarker Discovery
Haiyan
Zheng; Caifeng Zhao; Swapan Roy; Devjit Roy MD; Amenah Soherwardy;
Ravish Amin; Matthew Kuruc. Application Report -
The
Comparison of the Serum Proteome in Individuals with Cancers versus
those without Cancer, and its application to Wellness
Kuruc
Matt, Dr.Roy. Application Report -
AlbuVoid™
LC-MS On-Bead – Differential Expression of Cancer Sera Proteins
Using Quantitative (iTRAQ) Proteomics
Dr.Swapan
Roy; Amenah Soherwardy; Ravish Amin; Matthew Kuruc.Monmouth Junction,
NJ - Application Report.
AlbuSorb™
Product Extension Combines Albumin and Immunoglobulin Depletion in a
Consumable Format
ProCipitate™,
Superior Substitute to Phenol/Chloroform for DNA Isolation &
Protein Extraction
. by
Matt Kuruc February 23, 2015
The
Functional & Chemical Proteomics Handbook
Hemoglobin
Removal Reference Applications
Cleanascite™
Lipid Removal & Clarification Reference Applications
Albumin
Removal Reference Applications
Liquid Biopsy
Polack, M., et al. “Results from the UNITED study: a multicenter study validating the prognostic effect of the tumor–stroma ratio in colon cancer.” ESMO open. 9.4 (2024): 102988.
N. Diederiks, C.J. Ravensbergen, M. Treep, M. van Wezel, M. Kuruc, L. Renee Ruhaak, R.A.E. Tollenaar, C.M. Cobbaert, Y.E.M. van der Burgt, W.E. Mesker“Development of Tier 2 LC-MRM-MS protein quantification methods for liquid biopsies”Journal of Mass Spectrometry and Advances in the Clinical Lab (2022).
Ravensbergen, Cor J., et al. "“The Stroma Liquid Biopsy Panel Contains a Stromal-Epithelial Gene Signature Ratio That Is Associated with the Histologic Tumor-Stroma Ratio and Predicts Survival in Colon Cancer.” Cancers 14.1 (2022): 163.
Leiden
University Medical Center and Biotech Support Group Report Progress
on Stromal Conditioning Biomarkers in Cancer
“Stroma Liquid Biopsy™ - Blood-based biomarkers to monitor stromal
conditioning in cancer” at the Companion Diagnostics Forum, October 30, 2019 in Princeton NJ.
Stroma Liquid Biopsy™ - Blood-based biomarkers to monitor stromal conditioning in cancer.
Published February, 2019.
.
Haiyan
Zheng
1;
Swapan Roy
2;
Devjit Roy MD
2;
Amenah Soherwardy
1;
Seema Rathman
2;
Matthew Kuruc
21Rutgers
Center for Integrative Proteomics, Piscataway, NJ; 2Biotech Support
Group LLC, Monmouth Junction, NJ.
Application
Report: Stroma Liquid Biopsy – Pan-Cancer Dysregulation of the
Serum Proteome.
Biotech
Support Group described a panel of protein biomarkers dysregulated in
cancer at the recent HUPO World Congress, that took place September
17-21 in Dublin, Ireland. This research shows that there are three
common pathways which change in the bloodstream regardless of the
primary tumor, stage, metastatic disease, or tumor burden. Five
different cancers – lung, breast, pancreatic, lymph and ovary,
were profiled along with normal/healthy individuals of approximate
age and matched sex for comparison. The presentation is entitled
“Stroma Liquid Biopsy – Biomarkers of the Dysregulation
of the Serum Proteome in Cancer. It can be downloaded at:
Biotech
Support Group Presents Stroma Liquid Biopsy Cancer Data at HUPO World
Congress 2017
.
Poster
Reprint First Presented at New Jersey Cancer Retreat, May 25, 2017.
Haiyan Zheng(1), Swapan Roy(2), Amenah Soherwardy(1), Seema
Rahman(2), Matthew Kuruc(2); (1)Rutgers Center for Integrative
Proteomics, Piscataway, NJ; (2)Biotech Support Group LLC, Monmouth
Junction, NJ; entitled
"Stroma
Liquid Biopsy - Proteomic Profiles for Cancer Biomarkers"
.
Cell. 2011;144:646-674.
Zheng
H, Zhao C, Roy S, et al.
The
Comparison of the Serum Proteome in Individuals with Cancers versus
those without Cancer, and its application to Wellness
.
Poster reprint from 12th Annual US HUPO 2016 Conference, held March
13 – 16, 2016 Boston, MA, USA.
Zheng
H, Zhao C, Roy S, et al.
The
Commonality of the Cancer Serum Proteome Phenotype as analyzed by
LC-MS/MS, and Its Application to Monitor Dysregulated
Wellness.
Poster
reprint from AACR Annual Meeting 2016 Conference, held April 17-20,
2016 New Orleans, LA USA
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