VZV-Q Real-Time PCR Kit

Quantitative Detection of Varicella-Zoster Virus (VZV) by Real-Time PCR

The VZV-Q Real-Time PCR Kit is an in vitro diagnostic molecular assay designed for sensitive and specific quantitative detection of Varicella-zoster virus (VZV) specific DNA in clinical samples using real-time PCR technology. It supports accurate detection of VZV infection for clinical diagnosis and laboratory applications.

At a Glance

Product Overview


The VZV-Q Real-Time PCR Kit is based on TaqMan probe chemistry for the amplification and detection of VZV-specific DNA sequences. Fluorescent probes labelled with reporter and quencher dyes enable real-time monitoring of amplification.

The assay allows simultaneous detection of VZV DNA and an internal control (RNase P) using distinct fluorescence channels, ensuring assay reliability and validation of extraction and amplification steps.

Detection is performed across fluorescence channels and a positive control is included to verify proper assay setup, reagent integrity and amplification conditions.

VZV-Q  Comprehensive

How the Assay Works


The assay follows a standardized molecular workflow:

  • Sample Collection & Nucleic Acid Extraction: DNA is extracted from vesicular fluid or lesion swab samples using recommended extraction kits.
  • Real-Time PCR Amplification: Extracted DNA is amplified using VZV-specific primers in a real-time PCR system.
  • Fluorescent Detection: Amplification signals are detected in real time.
  • Quantification & Interpretation: Detection is based on Ct values and amplification curves for accurate result interpretation.

Key Features & Benefits


  • Quantitative detection of VZV DNA
  • TaqMan probe-based chemistry for high specificity
  • Multiplex detection (target + internal control)
  • Internal control ensures assay validation
  • Positive control for performance verification
  • Sensitive detection from lesion-based samples
  • Suitable for clinical diagnostic workflows

Why VZV Detection Matters


Varicella-zoster virus (VZV) is a human alpha herpesvirus responsible for both varicella (chickenpox) and herpes zoster (shingles).

  • • Primary infection causes varicella, characterized by fever and vesicular rash
  • • The virus remains latent in sensory nerve ganglia
  • • Reactivation leads to herpes zoster, often associated with age and immunosuppression

PCR is the most sensitive method for confirming VZV infection and can detect the virus in skin lesions such as vesicles, scabs, and maculopapular lesions. Compared to viral culture and DFA, PCR provides faster and more sensitive detection.

Targets Detected


VZV Target
  • Detection of Varicella-zoster virus DNA
Internal Control
  • RNase P (endogenous internal control)
  • Monitors nucleic acid extraction and amplification efficiency

Sample Type & Reporting Output


Sample Types
  • Vesicular fluid
  • Lesion swabs
Reporting Output
  • Quantitative detection of VZV DNA

Analytical Performance


Ct Cut-off Value:
≤ 35
Positive Control (VZV):
Ct value of 18 ± 2
Negative Control (NTC):
No amplification (Ct = 0)

Workflow advantage


Single-reaction setup with defined reagent volumes ensures consistency across runs
Multiplex detection of VZV target and internal control in a single reaction
Internal control (RNase P) integrated within assay design for validation
Pre-formulated reagents simplify assay setup
Closed-tube system minimizes contamination risk
Compatible with standard real-time PCR instruments

Storage and Stability


  • Shelf life: 12 months from date of manufacture
  • Storage temperature: -30°C to -10°C
  • Stable at -20°C until expiry
  • Avoid repeated freeze-thaw cycles (>6 times)
  • Protect from direct sunlight

Applications & Use Scenarios


The kit is intended for use in clinical laboratories for:

  • Detection of Varicella-zoster virus infection
  • Diagnosis of varicella and herpes zoster
  • Molecular testing of lesion-based samples
  • Routine diagnostic workflows

Ordering Information


Commercial Name Old Cat No. New Cat No. Pack Size
VZV-Q Real-Time PCR Kit G2M705821 50 Tests

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Since its inception in 2016, Genes2me has been constantly striving towards setting a benchmark in the diagnostics space by introducing premium quality (Made in India) diagnostic kits which are CE-IVD, ISO-13485:2016, and ISO 9001:2015 certified, assuring our clients of unparalleled quality and compliance with international standards.


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