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HemoVoid™ Advances Multi-omic Study of Thalassemia Severity An article let by researchers from The University of Burdwan, India utilized HemoVoid™ enrichment in a multi-omic study of thalassemia. Press Release
HemoVoid™ Advances Multi-omic Study of Thalassemia Severity
MONMOUTH JUNCTION, NJ, February 17, 2026– An article let by researchers from The University of Burdwan, India utilized HemoVoid™ enrichment in a multi-omic study of thalassemia. The citation is: Mitra, Nibedita, et al. "Multi-omics analysis of red blood cells reveals thalassemia severity beyond globin gene mutations." Blood Advances (2026): bloodadvances-2025016677.
TDT samples exhibited higher protein-to-transcript (PTRs) for ferroptosis-related proteins (FTH1, FTL, HMOX1) and lower PTRs for autophagy genes, suggesting impaired cellular recycling and enhanced oxidative cell death. PTR analysis showed reduced cytoskeletal (ankyrin, spectrin) expression, elevated chaperone activity, ferroptosis markers (FTH1, FTL, HMOX1), and suppressed autophagy. Collectively, these multilayered alterations—splicing dysfunction, post-transcriptional deregulation, ferroptosis, autophagy suppression, oxidative stress, and cytoskeletal fragility—underlie the greater disease severity observed in TDT compared with NTDT.
“This is an excellent study demonstrating how HemoVoid™ can be used in a multi-omic study comparing different disease severities. The HemoVoid™ product used in this study is one of many beads derived from our unique NRicher™ surface chemistry platform. With HemoVoid™ enrichment, the study was able to differentiate different patient cohorts by protein-to-transcript (PTR) associations. stated Dr. Swapan Roy, President and Founder of Biotech Support Group.
For more information on HemoVoid™ LC-MS On-Bead, visit: https://www.biotechsupportgroup.com/HemoVoid-LC-MS...
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Business Development Inquiries: Keywords: HemoVoid™, Hemoglobin depletion, Hemoglobin removal, Thalassemia, Red Blood Cell proteomics, protein-to-transcript (PTR), |

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Thalassemia
is classified as transfusion-dependent (TDT), requiring regular
transfusions, and non-transfusion-dependent (NTDT), which follows a
milder clinical course. This study aims to identify dysregulated
molecular pathways in red blood cells contributing to thalassemia
severity. RNA sequencing and proteome analysis were conducted on
isolated RBCs, through Novaseq and Orbitrap MS platform respectively.
For proteome analysis, the article states “A 75 µL RBC suspension
was used for protein extraction with RIPA buffer (Thermo Fisher
Scientific), and hemoglobin was depleted using the HemoVoid Kit
(Biotech Support Group, Cat. No. HVB-MS10)”.