M. PNEUMONIA-Q Real-Time PCR Kit

Qualitative Detection of Mycoplasma pneumoniae DNA

The M. PNEUMONIA-Q Real-Time PCR Kit is an in vitro diagnostic (IVD) molecular diagnostic test designed for the qualitative detection of Mycoplasma pneumoniae DNA from human respiratory clinical samples, including nasopharyngeal fluid, sputum, and throat swabs.

The assay enables rapid and accurate molecular detection of M. pneumoniae through a standardized automated Real-Time PCR workflow, supporting timely diagnosis, appropriate antimicrobial therapy, and improved clinical management of respiratory tract infections.

Product Overview

The M. PNEUMONIA-Q Real-Time PCR Kit is an advanced in vitro diagnostic (IVD) assay based on Real-Time PCR technology. The assay performs automated nucleic acid extraction, and DNA amplification using the OnePCR Ultra-Fast POC RT-PCR System.

The kit detects:

  • Mycoplasma pneumoniae DNA
  • Internal Control (IC) for assay validation and quality assurance

The assay utilizes an automated sample-to-result workflow that combines nucleic acid extraction and multiplex Real-Time PCR amplification into a single integrated process, providing rapid, reliable, and highly sensitive detection with minimal hands-on time.

M. PNEUMONIA-Q Real-Time PCR Kit

Why Mycoplasma pneumoniae Testing Matters

Mycoplasma pneumoniae is one of the leading causes of community-acquired pneumonia (CAP), particularly among children, adolescents, and young adults. Unlike most bacteria, it lacks a cell wall, making conventional microscopic examination ineffective and reducing the effectiveness of certain antibiotics such as beta-lactams. Because the organism grows slowly and requires specialized culture conditions, traditional culture-based diagnosis is often impractical for routine clinical use.

M. pneumoniae infection has also been associated with several respiratory and extrapulmonary complications, including bronchial asthma exacerbation, chronic obstructive pulmonary disease (COPD), acute respiratory distress syndrome (ARDS), polyarthritis, Guillain-Barré syndrome, stroke, and coronary artery disease. Rapid molecular detection is therefore essential for early diagnosis, timely treatment, and effective patient management.

The M. PNEUMONIA-Q Real-Time PCR Kit helps laboratories to:

Targets Detected

Qualitative Targets
  • Mycoplasma pneumoniae DNA
Internal Control
  • Internal Control (IC)
    Ensures successful DNA extraction, assay integrity, amplification efficiency, and reliable result reporting for every processed sample.

Applications

The kit is ideal for clinical molecular laboratories performing:

M. pneumoniae-Q Real-Time PCR Kit
  • Molecular detection of Mycoplasma pneumoniae
  • Early diagnosis of community-acquired pneumonia
  • Confirmation of suspected atypical pneumonia
  • Routine respiratory pathogen molecular testing
  • Infectious disease molecular diagnostic workflows

Key Features & Benefits

Automated Sample-to-Result Workflow

Integrated with the OnePCR Ultra-Fast POC RT-PCR System for automated DNA extraction, and amplification significantly reducing manual handling and turnaround time.

Sensitive and Specific Detection

Utilizes highly specific primers and fluorescent probe-based chemistry for accurate detection of Mycoplasma pneumoniae DNA.

Multiplex Real-Time PCR Assay

Simultaneously detects the Mycoplasma pneumoniae target together with the Internal Control in a single automated workflow.

Built-in Internal Control for Quality Assurance

The integrated Internal Control verifies successful nucleic acid extraction, reaction performance, and assay validity.

Optimized for Routine Clinical Testing

Designed for rapid and reliable molecular diagnosis in clinical laboratories, hospitals, emergency departments, and decentralized Point-of-Care testing settings.

Sample Types & Reporting Output

Sample Types

Validated for use with:

  • Nasopharyngeal fluid
  • Sputum
  • Throat swab
Reporting Output

The test provides clear and actionable laboratory results, including:

  • Positive / Negative interpretation
  • Ct values
  • Amplification curves
  • Internal Control status
  • Result export options (USB or Bluetooth via OnePCR System)

Compatible System

OnePCR Ultra-Fast RT PCR System

Designed for fully automated nucleic acid extraction, amplification, fluorescence detection, and result interpretation in an integrated sample-to-result workflow.

ONEPCR Automated Testing Workflow
  • Collect nasopharyngeal fluid, sputum, or throat swab specimen.
  • Load 200 µL of the sample into Cartridge-1.
  • Reconstitute Cartridge-2 by adding 10 µL Reconstitution Buffer.
  • Load Cartridge-1 and Cartridge-2 into the OnePCR Ultra-Fast POC RT-PCR System.
  • The system automatically performs DNA extraction and Real-Time PCR amplification.
  • Results are displayed as Positive/Negative together with Ct values and amplification curves.

Storage & Stability

Ordering Information

Commercial Name Old Cat No. New Cat No. Pack Size
M. PNEUMONIA-Q Real-Time PCR Kit G2M707721R 24 Tests

Why Choose the M. PNEUMONIA-Q Real-Time PCR Kit?

If your laboratory requires a reliable molecular assay for rapid detection of Mycoplasma pneumoniae DNA, the M. PNEUMONIA-Q Real-Time PCR Kit delivers:

  • fully automated DNA extraction and Real-Time PCR workflow
  • highly sensitive and specific fluorescent probe-based detection
  • integrated Internal Control for assay validation
  • rapid and reliable molecular diagnosis
  • minimal hands-on time with an automated sample-to-result workflow
  • suitability for routine respiratory pathogen molecular diagnostics
  • seamless integration with the OnePCR Ultra-Fast POC RT-PCR System

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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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