InnoAmp HCV Quantitative Real-Time PCR Kit

The InnoAmp HCV Quantitative Real-Time PCR Kit detects and quantifies Hepatitis C Virus RNA in patient samples with precision. Genotype-agnostic and traceable to WHO International Standards, it supports diagnosis, treatment monitoring, and confirmation of sustained virologic response.

FORMAT

Real-Time PCR

PREPS

50 Reactions

SAMPLE VOLUME

40 IU/mL to 10^7 IU/mL

Pack Size (Reactions): 25 Reactions (MBRT-03 25T)

QUICK HIGHLIGHTS

Genotype-Agnostic Detection (Genotypes 1 to 6)
Detection Limit of 40 IU/mL
Wide Dynamic Range up to 10^7 IU/mL
WHO International Standard Traceable
Compatible with Standard qPCR Platforms
Results Within a Few Hours

KIT OVERVIEW

Precise HCV Viral Load Quantification for Every Stage of Care

Hepatitis C Virus (HCV) infection is a leading cause of chronic liver disease, cirrhosis, and hepatocellular carcinoma. While antibody screening indicates previous exposure, HCV RNA testing confirms active infection and supports treatment monitoring. Accurate viral load quantification is essential for diagnosis, therapeutic decision-making, and assessment of treatment response.

The InnoAmp HCV Quantitative Real-Time PCR Kit uses TaqMan-based real-time PCR to quantify HCV RNA across all major genotypes (1 to 6) and their subtypes. Primers and probes target conserved regions of the HCV genome, ensuring reliable detection regardless of the genotype circulating in the patient population. Results are expressed in International Units per millilitre (IU/mL), directly traceable to the WHO International Standard for HCV RNA, so viral load data is comparable across labs and studies.

Technology

Real-Time Quantitative PCR (qPCR) with TaqMan Chemistry

Target

HCV RNA, conserved genomic regions

Genotype Coverage

All major genotypes (1 to 6) and subtypes

Limit of Detection

40 IU/mL

Quantitative Range

40 IU/mL to 10^7 IU/mL

WHY INNOAMP HCV

Genotype-Agnostic Detection

Detects HCV RNA across major genotypes 1 to 6 using primers and probes targeting conserved genomic regions.

WHY INNOAMP HCV

High Analytical Sensitivity

Supports sensitive HCV RNA detection with a limit of detection of 40 IU/mL.

WHY INNOAMP HCV

Wide Quantitative Range

Enables viral load quantification across a broad range from 40 IU/mL to 10⁷ IU/mL.

WHY INNOAMP HCV

WHO Standard Traceability

Reports HCV viral load in IU/mL with traceability to the WHO International Standard for HCV RNA.

WHY INNOAMP HCV

Reliable Viral Load Monitoring

Supports HCV diagnosis, treatment monitoring, and assessment of sustained virologic response.

THE PROCESS

Simple Steps Pure Results

HOW IT WORKS

Step 1 - Sample Collection

Collect patient serum or plasma using standard clinical protocols.

HOW IT WORKS

Step 2 - RNA Extraction

Extract HCV RNA using a validated extraction method compatible with downstream real-time PCR.

HOW IT WORKS

Step 3 – PCR Setup

Prepare the reaction using HCV-specific primers, probes, and master mix. Include positive, negative, and HCV RNA standards to calibrate quantification.

HOW IT WORKS

Step 4 – Amplification and Quantification

Run on a compatible real-time PCR platform. Viral load is reported in IU/mL, traceable to the WHO International Standard.

Supporting callouts (below steps)

  • Covers all major HCV genotypes
  • Results in a few hours
  • WHO-traceable quantification

Quick Answers
Here

Find quick answers about the InnoAmp HCV Quantitative Real-Time PCR Kit, including genotype coverage, dynamic range, compatibility, and ordering.

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Where Accuracy Meets Accessibility

Diagnostic solutions built for laboratories, hospitals, and healthcare institutions, designed for real-world testing needs.

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