HPV-Q Real Time PCR Kit | Rapid POCT | Reproductive Health Screening Kits

Product Overview

The HPV-Q Real Time PCR Kit is an in vitro diagnostic (IVD) assay based on real-time PCR technology for detection of high-risk HPV DNA from clinical samples. The assay integrates automated nucleic acid extraction, multiplex real-time PCR amplification and Fluorescent probe-based detection within a fully automated workflow on compatible systems.

The kit is designed as a single-tube multiplex assay, enabling simultaneous detection of multiple HPV genotypes along with an internal control, ensuring reliable and efficient testing.

Why HPV Testing Matters

Human Papillomavirus (HPV) is one of the most common sexually transmitted infections and is the primary cause of cervical cancer.

HPV-16 and HPV-18 account for ~70% of cervical cancer cases
Persistent high-risk HPV infection can lead to precancerous lesions
HPV is also associated with other cancers (anal, vaginal, vulvar, penile, and oropharyngeal)
Early detection enables timely intervention and improved outcomes

Molecular testing using real-time PCR allows accurate detection of high-risk HPV types, supporting screening, diagnosis, and clinical decision-making.

Targets Detected ( High-Risk HPV Genotypes )

Individually Detected:

HPV-16
HPV-18

Pooled Detection (High-Risk Types):

HPV 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68

Internal Control

Beta-actin gene ensuring sample adequacy, extraction efficiency, and assay validity

Applications

The kit is ideal for clinical molecular laboratories performing:

HPV molecular testing
Cervical cancer screening programs
Detection of high-risk HPV infections
Women’s health diagnostics
Oncology risk assessment
Public health screening initiatives

Key Features & Benefits

Comprehensive High-Risk HPV Detection

Covers 14 clinically relevant high-risk HPV genotypes in a single assay.

Single-Tube Multiplex Real-Time PCR

Enables simultaneous detection of multiple targets with reduced handling steps.

Differentiation of HPV-16 & HPV-18

Allows specific identification of the two most oncogenic HPV types.

Probe-Based Detection for High Specificity

Fluorescent probes ensure accurate and reliable amplification detection.

Automated Extraction-to-Result Workflow

Compatible with OnePCR system for streamlined, user-friendly operation.

Rapid and Efficient Testing

Supports timely screening and diagnosis in clinical workflows.

Sample Types & Reporting Output

Sample Types

Validated for use with Cervical swab samples.

Cervical swab samples
Samples should be collected using appropriate collection devices and transported at 2–8°C, with processing within recommended timelines to ensure DNA integrity.

Reporting Output

The assay provides clear qualitative reporting, including:

HPV-16 Positive / Negative
HPV-18 Positive / Negative
High-risk HPV pool Positive / Negative
Ct values for each target
Amplification curves
Internal control validation
Exportable reports via USB or Bluetooth

Compatible System

OnePCR Ultra-Fast RT PCR System

Designed for automated workflow including extraction and amplification.

Collect cervical swab sample
Load 200 µl sample into Cartridge-1
Reconstitute Cartridge-2 ready mix
Insert cartridges into the system
Automated DNA extraction + real-time PCR
Results displayed with Ct values and interpretation

Ordering Information

Commercial Name	Old Cat No.	New Cat No.	Pack Size
HPV-Q Real Time PCR Kit (SKU 1)	G2M706721R	G610013-3	24 Tests
HPV-Q Real Time PCR Kit (SKU 2)	G2M706721R	G610013-6	24 Tests
HPV-Q Real Time PCR Kit (SKU 3)	G2M706721R	G610013-9	24 Tests

Why Choose the HPV-Q Real Time PCR Kit?

If your laboratory requires a reliable HPV multiplex PCR kit for high-risk genotype detection, this assay delivers:

detection of 14 high-risk HPV genotypes in one test
specific identification of HPV-16 and HPV-18
single-tube multiplex workflow for efficiency
high specificity with probe-based PCR chemistry
internal control validated results
automated extraction-to-result integration
suitability for cervical cancer screening and molecular diagnostics

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.

Multiplex Detection of High-Risk Human Papillomavirus (HPV) by Real-Time PCR

Product Overview

Why HPV Testing Matters