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Pseudorabies Virus (PRV/SuHV-1) Research Reagents — Antibodies & Recombinant Proteins

Pseudorabies virus (PRV, also known as Suid herpesvirus 1/SuHV-1, or Aujeszky's disease virus) is an enveloped, double-stranded DNA alphaherpesvirus (~143 kb genome) that causes Aujeszky's disease in swine — a notifiable disease (OIE/WOAH) characterized by respiratory illness, reproductive failure, and fatal encephalitis in piglets. PRV is also a premier model organism for studying herpesvirus neurotropism, axonal transport, transynaptic tracing of neural circuits (Bartha strain), and alphaherpesvirus entry mechanisms. The PRV envelope contains at least 11 glycoproteins; gD (US6, receptor binding via nectin-1), gB (class III fusogen), gH/gL (fusion trigger), and gC (complement evasion/GAG binding) are the primary targets for neutralizing antibodies and vaccine development. Glycoprotein E (gE) is deleted in marker vaccines (gene-deleted DIVA vaccines) and is the standard DIVA serology antigen for eradication programs.

Research Use OnlyNot for diagnostic or therapeutic use.

abinScience offers the most comprehensive PRV/SuHV-1 reagent portfolio available — covering seven envelope glycoproteins (gB, gD, gE, gH, gL, gM, gC) plus UL42/PAP (processivity factor, 6 recombinant antibody clones) — including InVivoMAb neutralizing antibodies, recombinant proteins in multiple tag formats, and polyclonal detection antibodies. Manufactured by AtaGenix Laboratories (ISO 9001 & ISO 13485). Contact us for DIVA assay reagents and bulk orders.

Entry Glycoproteins — gD, gB, gH/gL

Glycoprotein D (gD/US6) — Receptor Binding
gD binds nectin-1 to trigger viral entry and is the primary PRV vaccine immunogen. Available: recombinant gD proteins — C-His (VK437011) and N-His (VK437012); and anti-gD polyclonal antibody (VK437014).

Glycoprotein B (gB/UL27) — Class III Fusogen
gB is the conserved herpesvirus fusion protein essential for membrane fusion. abinScience provides the deepest anti-PRV gB reagent set: InVivoMAb neutralizing antibodies Iv (VK597010) and Iv (VK597020); recombinant gB proteins — C-His (VK597011), C-His (VK049011), and N-His (VK049012); and anti-gB polyclonal antibody (VK049014).

Glycoprotein H/gL — Fusion Trigger Complex
gH/gL heterodimer triggers gB conformational change for membrane fusion. Available: InVivoMAb anti-gH D6.3 (VK485010); gH recombinant proteins — C-His (VK047011) and N-His (VK047012); anti-gH pAb (VK047014); and gL recombinant protein C-Strep (VK048011).

gE, gC, gM — Immune Evasion & DIVA Diagnostics

Glycoprotein E (gE) — DIVA Serology Antigen
gE is deleted in all major PRV marker vaccines (Bartha, Begonia, NIA-3 gE⁻) used in eradication programs worldwide. Detection of anti-gE antibodies differentiates field-infected animals from vaccinated animals (DIVA principle). gE recombinant protein is the standard ELISA coating antigen for DIVA serology. Available: gE C-Strep (VK711011), gE N-His-SUMO (VK711012), and anti-gE polyclonal antibody (VK711014).

Glycoprotein C (gC) & Glycoprotein M (gM)
gC binds complement C3b and heparan sulfate, mediating complement evasion and initial cell attachment. gM is essential for virion envelopment and egress. Available:
• gC: N-His-KSI (VK051012) and anti-gC pAb (VK051014)
• gM: N-His-KSI (VK050012) and anti-gM pAb (VK050014)

UL42/PAP — Processivity Factor (6 Antibody Clones)

UL42 (polymerase accessory protein/PAP) is the DNA polymerase processivity factor essential for viral DNA replication. UL42 is a validated antiviral drug target — disrupting UL42–polymerase interaction blocks viral replication. abinScience offers the deepest anti-UL42 antibody panel available for any herpesvirus:

6 Recombinant Antibody Clones
2G11 (VK649013), 7C11 (VK649023), 8F9 (VK649033), 5F8 (VK649043), 2D5 (VK649053), and 4E2# (VK649063) — enabling epitope mapping, functional blocking studies, and competition binning of the UL42-polymerase interaction interface.

UL42 Proteins & Polyclonal Antibodies
Domain-specific recombinant proteins: UL42 (1-148) N-His (VK649012) and UL42 (256-384) N-His (VK649022); polyclonal antibodies VK649014 and VK649024.

Frequently Asked Questions

Which reagents are needed for PRV DIVA serology?
DIVA (Differentiating Infected from Vaccinated Animals) relies on detecting anti-gE antibodies — present in field-infected pigs but absent in animals vaccinated with gE-deleted marker vaccines (Bartha, etc.). Use gE C-Strep (VK711011) or gE N-His-SUMO (VK711012) as ELISA coating antigen, with anti-gE pAb (VK711014) as positive control.

Which antibodies are recommended for PRV neutralization studies?
For gB-mediated fusion blockade: InVivoMAb antibodies VK597010 and VK597020. For gH-mediated fusion triggering: InVivoMAb D6.3 (VK485010). Combining anti-gB + anti-gH provides synergistic neutralization. All InVivoMAb antibodies are produced low-endotoxin, azide-free for in vivo use.

Can PRV reagents be used for neural circuit tracing research?
Yes. PRV (particularly the Bartha strain) is the gold-standard retrograde transynaptic tracer for mapping neural circuits. Our gB, gD, gH, and gE antibodies can be used to detect PRV-infected neurons by IHC and immunofluorescence in brain tissue sections, confirm viral spread directionality, and characterize recombinant PRV tracer variants.

Why do you have 6 antibody clones against UL42?
UL42/PAP is an attractive antiviral target — small molecules that disrupt the UL42-polymerase interaction can block viral DNA replication. Having 6 clones targeting different epitopes enables detailed mapping of the UL42-polymerase binding interface, competition assays for drug screening, and identification of functional domains critical for processivity factor activity.

Related Herpesvirus & Swine Virus Reagents

Explore reagents for related viruses:

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