BK polyomavirus (BKPyV, formerly BK virus/BKV) is a small, non-enveloped, circular double-stranded DNA polyomavirus (~5.1 kb genome) that infects over 90% of the global population during early childhood, establishing lifelong latency in renal tubular epithelial cells and the urothelium. BKPyV is clinically silent in immunocompetent individuals but reactivates under immunosuppression — causing polyomavirus-associated nephropathy (PVAN/BKVN) in 1–10% of kidney transplant recipients (the leading infectious cause of renal allograft loss) and hemorrhagic cystitis in hematopoietic stem cell transplant (HSCT) patients. There are currently no approved antivirals for BKPyV; management relies on reduction of immunosuppression. The BKPyV genome encodes the major capsid protein VP1 (receptor binding via gangliosides GT1b/GD1b, primary neutralization target), the minor capsid proteins VP2/VP3, large T antigen (LTag, oncogenic driver, replication initiator), small T antigen (sTag), and agnoprotein (viral assembly/egress). VP1 is the basis for serology, neutralization assays, and all therapeutic antibody candidates currently in clinical development.
Research Use OnlyNot for diagnostic or therapeutic use.
abinScience offers a focused BKPyV reagent portfolio centered on the VP1 capsid protein — including a biosimilar-grade reference antibody (Traxivitug), 5 recombinant anti-VP1 neutralizing antibody clones, VP1 recombinant proteins, plus Large T antigen and agnoprotein — enabling transplant nephrology research, therapeutic antibody development, and serological assay design. Manufactured by AtaGenix Laboratories (ISO 9001 & ISO 13485). Contact us for genotype-specific VP1 proteins and bulk orders.
Major Capsid Protein VP1 — Neutralization & Therapeutic Target
VP1 pentamers form the icosahedral capsid (72 pentamers per virion) and mediate receptor binding via sialylated gangliosides (GT1b, GD1b). VP1 is the sole target for neutralizing antibodies and the basis for all BKPyV therapeutic antibodies in clinical development. VP1 serotypes (genotypes I–IV) determine antibody specificity and cross-neutralization breadth. abinScience provides the deepest anti-VP1 antibody panel available:
• Biosimilar-grade reference antibody: Traxivitug (VK698016) — sequence-identical to the clinical-stage anti-BKPyV VP1 therapeutic antibody for PK/ADA/bioactivity reference
• Recombinant anti-VP1 neutralizing antibodies: MTX-005 (VK452013), 336F07 (VK452023), 319C07 (VK452033), P8D11 (VK452043), MAU868 (VK452053), and SAA3067 (VK452063)
• Recombinant VP1 proteins: C-His (VK452011) and N-MBP&C-His (VK698032) — MBP-tagged version enhances VP1 solubility for pentamer assembly studies
Large T Antigen (LTag)
LTag is the multifunctional regulatory protein that drives viral DNA replication (origin binding, helicase activity) and cell cycle dysregulation (pRb/p53 inactivation). LTag-mediated oncogenic transformation is the basis for BKPyV-associated urothelial carcinoma research. Available: recombinant LTag protein N-His (VK798012).
Agnoprotein — Viral Assembly & Egress
Agnoprotein is a small (~8 kDa) late-expressed protein essential for viral assembly, nuclear egress, and virion release. Agnoprotein is a unique feature of BKPyV and JCPyV (not present in SV40 or MCPyV) and a potential antiviral target. Available in three formats: N-His-SUMO (VK523012), N-His (VK523022), and N-His-SUMO variant (VK523032).
What is Traxivitug and how is it used?
Traxivitug (VK698016) is a research-grade antibody with a sequence identical to the clinical-stage anti-BKPyV VP1 therapeutic antibody being developed for PVAN prevention in kidney transplant recipients. It is intended for use as a positive control in neutralization assays, PK/ADA assay reference standard, and bioactivity benchmark in BKPyV therapeutic development programs.
Which VP1 protein format is best for serology ELISA?
VP1 C-His (VK452011) is recommended for direct ELISA plate coating. VP1 naturally assembles into pentamers and virus-like particles (VLPs) — conformational epitopes on assembled VP1 are the primary targets for neutralizing antibodies. The MBP-tagged VP1 (VK698032) may enhance solubility for applications requiring monomeric VP1.
Do your anti-VP1 antibodies cross-react with JC polyomavirus (JCPyV)?
BKPyV and JCPyV VP1 share ~78% amino acid identity. Some broadly reactive clones (e.g., P8D11) may cross-react, while genotype-specific clones may not. Contact us for clone-specific cross-reactivity data with JCPyV and SV40.
Why are there 6 different anti-VP1 antibody clones?
BKPyV VP1 has four major genotypes (I–IV) with variable loop regions that affect antibody binding. Having multiple clones targeting different VP1 epitopes enables: (1) identification of broadly neutralizing antibodies covering all genotypes; (2) epitope competition/binning for therapeutic cocktail design; (3) matched pair selection for VP1-capture sandwich ELISA development.
Explore reagents for related viruses in transplant medicine:
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