Viraffinity™ - Virus and Viral Component Isolation

Viraffinity™

  • Purifies whole infectious non-enveloped virus & non-infectious enveloped virus
  • Isolates antigenic virions, enveloped and non-enveloped
  • Enriches for viral nucleic acids
  • Prepares viral samples for subsequent detection and analysis

Viraffinity™ is a unique water-insoluble elastomeric polyelectrolyte that has been engineered for the capture and recovery of viruses. Applications include: purification of whole infectious non-enveloped virus, virions, viral components, and sample preparation for subsequent detection and analysis. Viraffinity™ is directly added to the sample that is then mixed and centrifuged. The centrifuged pellet contains polyelectrolyte-bound viruses that can then be recovered using a moderately alkaline pH solution. Viraffinity™ is supplied as a suspension reagent ready for use. Simply pipette the suspension into the sample at the appropriate ratio, typically 1 volume of Viraffinity™; to 4 volumes sample. Viraffinity™ is also supplied as the enabling component of the ViraPrep™ application kits.

Click here for Viraffinity™ Product Sheet

Composition and utility patents for Viraffinity™ and related technologies.

Composition and utility patents for Viraffinity™ and related technologies are covered under U.S. Patent Numbers 5,294,681 and other patents pending.

Composition and utility patents for Viraffinity™ and related technologies are covered under U.S. Patent Number 5,453,493 and other patents pending.

Composition and utility patents for Viraffinity™ and related technologies are covered under U.S. Patent Number 5,658,779 and other patents pending.

Metagenomic Analysis of the Human Mouth Virus Population and Characterisation of Two Lytic Viruses, Al-Jarbou, Ahmed, Theses, Dept. of Infection, Immunity and Inflammation

An isometric virus of the potato tuber moth Tecia solanivora (Povolny) (Lepidoptera: Gelechiidae) has a tri-segmented RNA genome Jean-Louis Zeddam et. al Journal of Invertebrate Pathology, Volume 99, Issue 2, October 2008, Pages 204-211

Activity of the Small Modified Amino Acid -Hydroxy Glycineamide on In Vitro and In Vivo Human Immunodeficiency Virus Type 1 Capsid Assembly and Infectivity Antimicrobial Agents and Chemotherapy, October 2008, p. 3737-3744, Vol. 52, No. 10 Samir Abdurahman

Mutation in the loop C-terminal to the cyclophilin A binding site of HIV-1 capsid protein disrupts proper virus assembly and infectivity Samir Abdurahman , Stefan Höglund , Anders Höglund and Anders Vahlne Retrovirology 2007, 4:19doi:10.1186/1742-4690-4-19

Detection Methods for Human Enteric Viruses in Representative Foods. Leggitt, Paris R.1; Jaykus, Lee-Ann, Journal of Food Protection®, Volume 63, Number 12, December 2000 , pp. 1738-1744(7).

Rapid Detection of Foodborne Viruses from Minimally Processed Foods.Microbial Detection Methods 2000

Mihalic, K. A., et al, Development of a Chemiluminescent Western Blot for Detecting Hantaan-Specific Antibodies, poster American Society of Tropical Medicine and Hygiene Meeting, October 1997.

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. InAbstracts of the 97th General Meeting of the American Society for Microbiology 1997, American Society for Microbiology, Washington, D.C.

Hitti, J., et al, Fast and Convenient Purification of Bacteriophage Lambda DNA with Viraffinityä Matrix, poster Cold Spring Harbor Conference on Genome Mapping & Sequencing, May 1997.

Ting, W. T. E., et al, The Use of Viraffinity Matrix to Concentrate Waterborne Polioviruses For RT-PCR Detection, poster American Society of Microbiology, May 1997.

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