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Multiplex qPCR Porcine Virus Panel

The Multiplex NGS Porcine Virus Panel leverages next-generation sequencing to detect a comprehensive range of porcine viruses, making it an essential tool for assessing adventitious agent risk in porcine-derived materials. Developed to support the safety of therapeutics and biologics exposed to porcine-derived materials, this service combines broad viral detection with the sensitivity and precision of deep sequencing. Our validated pipeline ensures confident results and regulatory readiness under GLP/GMP environments.

Adventitious Viruses

Virus Acronym

Virus Name

pADVB

Porcine adenovirus B

PCMV

Porcine cytomegalovirus

PRV

Pseudorabies virus

PLHV

Porcine lymphotropic herpesvirus

PPV1

Porcine parvovirus 1

PCV1

Porcine circovirus type 1

PCV2

Porcine circovirus type 2

PCV3

Porcine circovirus type 3

REV

Reovirus

BVDV

Bovine viral diarrhea virus

EV-G

Enterovirus G

RABV

Rabies virus

TGEV

Transmissible gastroenteritis virus

HEV

Hepatitis E virus

HEV

Porcine hemagglutinating encephalomyelitis virus

PRRSV1

Porcine reproductive and respiratory syndrome virus 1

Key Features

  • Comprehensive panel coverage: 16 porcine viruses
  • Quick turnaround time: 5 – 10 business days
  • High specificity
  • High sensitivity: LOD 5 – 10 copies
  • GMP/GLP compliant

Applications

The Multiplex qPCR Human Virus Panel is designed to support viral safety testing across a broad range of therapeutic and biologic workflows such as:

  • Cell/ gene therapy manufacturing
  • Raw material qualification
  • Lot release testing

Technical Specifications

Parameter

Details

Platform

qPCR

Detection Targets

22 Validated human viruses

Assay Format

Multiplex – multiple viral targets per reaction

Sensitivity (LOD)

As low as 5 – 10 copies/reaction

Specificity

High target specificity with minimal cross-reactivity

Sample Types

Cell culture supernatant, viral stocks, nucleic acid extracts, drug substance

Minimum Input Volume

Per multiplex assay- Cells: 200 uL with 106 cells; liquid: 200 uL

Turnaround Time

10 business days; RUSH 5 business days

Controls Included

Internal extraction control, positive and negative assay controls

Data Output

Ct values, presence/absence calls, assay QC data

Regulatory & Compliance

Our Multiplex qPCR Human Virus Panel is fully validated to support biosafety testing in regulated environments and meets the expectations of global health authorities.

Key compliance features include:

  • GMP and GLP compliance
  • 21 CFR Part 11 compliance

Have Questions?

We are dedicated to timely, high-quality service from the start of your project to the finish. Send us a quick message with your questions to find out what Avance can do for you.

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