B. Pertussis-Q Real Time PCR Kit

Qualitative Detection of Bordetella pertussis by Real-Time PCR

The B. Pertussis-Q Real Time PCR Kit is a CE-IVD molecular diagnostic assay designed for the qualitative detection of Bordetella pertussis DNA, the causative pathogen of pertussis (whooping cough), in clinical respiratory samples.

This assay enables rapid and sensitive molecular detection of Bordetella pertussis, supporting early diagnosis, timely treatment decisions, and effective infection control through a real-time PCR workflow.

Product Overview


The B. Pertussis-Q Real Time PCR Kit is an in vitro diagnostic (IVD) assay based on real-time PCR technology for the detection of Bordetella pertussis DNA from clinical samples.

The assay integrates automated DNA extraction (on compatible systems), Real-time PCR amplification and Fluorescent probe-based detection into a streamlined molecular diagnostic workflow.

The test targets specific DNA sequences of Bordetella pertussis, enabling reliable pathogen identification directly from respiratory specimens.

Why Bordetella pertussis Testing Matters


Bordetella pertussis is a highly contagious bacterial pathogen responsible for pertussis (whooping cough), a respiratory disease that spreads through respiratory droplets.

Symptoms often progress through stages including:

Infants and young children are particularly vulnerable, and complications may include:

Molecular detection using real-time PCR provides a rapid and sensitive method for identifying the pathogen, enabling early diagnosis and appropriate clinical management.

Targets Detected


Bacterial Target
  • Bordetella pertussis DNA
Internal Control
  • Internal control gene ensuring DNA extraction quality and assay validity.

Applications


The kit is suitable for clinical molecular laboratories performing:

RT-PML-RARA
  • Pertussis molecular testing
  • Detection of Bordetella pertussis infections
  • Respiratory pathogen diagnostics
  • Outbreak investigation and surveillance
  • Hospital and public health screening programs

Key Features & Benefits


Sensitive Molecular Detection of Pertussis

Detects Bordetella pertussis DNA directly from respiratory samples with high specificity.

Probe-Based Real-Time PCR Technolog

Fluorescent probe detection provides accurate amplification monitoring and reliable results.

Automated Extraction-to-Result Workflow

Compatible with automated systems that integrate DNA extraction and PCR amplification.

Rapid Detection for Early Diagnosis

Supports timely diagnosis of pertussis infections and improved patient management.

CE-IVD Validated Assay

Designed for use in professional clinical laboratories.

Sample Types & Reporting Output


Sample Types

Validated for respiratory specimens including:

  • Nasopharyngeal swabs
  • Oropharyngeal swabs

Samples should be transported and stored under recommended conditions to preserve nucleic acid integrity.

Reporting Output

The assay provides clear qualitative reporting, including:

  • Positive / Negative result for Bordetella pertussis
  • Ct values for detected targets
  • Amplification curves
  • Internal control validation
  • Exportable reports via USB or Bluetooth (system dependent)

Compatible System


OnePCR-Rapi-Q Ultra-Fast POC System

Designed for automated workflow including extraction and amplification.

OnePCR® workflow
  • Collect Naso/Oro pharyngeal swab samples
  • Load 200 µl sample into Cartridge-1
  • Reconstitute Cartridge-2 reagents
  • Insert cartridges into the system
  • Automated DNA extraction + real-time PCR amplification
  • Results displayed with Ct values and amplification curves

Storage & Stability


Ordering Information


Commercial Name Old Cat No. New Cat No. Pack Size
B. Pertussis-Q Real Time PCR Kit G2M706821R 24 Tests

Why Choose the B. Pertussis-Q Real Time PCR Kit?


If your laboratory requires a reliable pertussis PCR diagnostic kit, this assay provides:

  • sensitive detection of Bordetella pertussis DNA
  • rapid molecular confirmation of pertussis infection
  • probe-based real-time PCR accuracy
  • internal control validated results
  • automated extraction-to-result workflow
  • suitability for clinical diagnostics and respiratory infection surveillance

Product Enquiry Form


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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