Mycoplasma Pneumoniae Nucleic Acid Detection Kit (Fluorescent PCR)

BI-BSJ-09

Mycoplasma pneumoniae (MP) is a bacterial pathogen associated with community-acquired pneumonia (CAP) in children and adults. It causes respiratory diseases and is transmitted through droplets, aerosols, or direct contact. Therefore, the ability to monitor Mycoplasma pneumoniae is of tremendous clinical importance. This kit is used for qualitative detection of Mycoplasma pneumoniae in oropharyngeal swab specimens from suspected cases. It has good specificity and high sensitivity. The reaction in this kit contains a dUTP-UDG enzyme anti-pollution system to help prevent false positive results. For quality assurance of the entire extraction and detection process, human RNaseP gene is used as a non-competitive internal control. The kit can be used with the Gene Bio Medical Fluorescence Quantitative PCR Detection System, LineGene 9600 Plus (FQD-96A), or QuantGene 9600 (FQD-96C).

Product Features

  • Strong applicability:Suitable for human pharyngeal swabs.
  • Good specificity: No cross reactivity has been observed by testing the clinical positive specimens such as Ureaplasma Urealyticum, Influenza A (HIN1), Influenza B (Victoria), Respiratory Syncytial Virus A/B, Parainfluenza Type 3, etc.
  • High sensitivity: Three different batches of reagents were used to test and the sensitivity can reach to 200 copies/mL.
  • Excellent anti-interference ability: Endogenous inhibitors (such as blood, mucin, and nasal secretions) and exogenous inhibitors (such as common drugs for treating colds or other similar symptoms) showed no influence on the detection.
  • High Precision: Positive controls and low positive controls reference were tested by 3 lots of kits with 10 replicates by 2 operators for 20 days. The results showed that the variation coefficient (CV) of within-day, between-day, within-batch and between-batch were less than 5%.
  • Simple operation:The PCR test can be finished within 32 min.