Cpn Colloidal Gold Rapid Test Chlamydia Pneumoniae Diagnostic Test

Chlamydia pneumoniae(Cpn) Rapid Tests

• Chlamydia pneumonia
  (Cpn)-IgM antibody
  Catalog No.: BG1101C

  Packing specification
  20 test cards/ box

  Intended Use

  This kit is used to qualitatively detect the existence of Cpn -IgM antibodies in serum or plasma sample, as an auxiliary clinical diagnostic reagent of Cpn infection in early stage. Chlamydia pneumoniae (Cpn) is a species of Chlamydophila, an obligate intracellular bacterium that infects humans and a major cause of pneumonia. It is mainly infected through the respiratory transmission and can breed in human alveolar macrophages, epithelial cells, endothelial cells, smooth muscle cells and neutrophils. Chlamydia pneumoniae is the main cause of the human atypical pneumonia, bronchitis, pharyngitis, sinusitis, otitis media, iritis, myocarditis and other diseases. 5-10% of the community acquired pneumonia, bronchitis and sinusitis was caused by chlamydia pneumoniae. In addition, epidemiology and aetiology research shows that the chlamydia pneumoniae infection is associated with cardiovascular disease.

  Test Procedure
  1.Test preparation: 10μL, 100μL micropipettes and matched tips
  2.Test process: The temperature of the kit and the test sample should be the same with room temperature before test. Place the test card on a dry horizontal work surface. Add 10μL serum or plasma sample into the sample well, then add 100 μL of sample dilution immediately. Observe the result in 15-20 minutes after the serum or plasma samples added. The observation is invalid after 20 minutes.

  Test results explain

  
  

  

  
  

  

  
  

  To develop color on C line only: negative; To develop color on both C line and T line: positive; To develop color on T line only: invalid; Not to develop color on both C line and T line: invalid.
  Note: Re-detection if the detection result is invalid. The invalid test cards should be dealt as infectious pollutants. The temperature of the kit and the test sample should be the same with room temperature before pre-detection.

Biovantion Inc is independent from international department of Bioneovan Co., Ltd., which established in 2 0 0 5, is an in vitro diagnostic reagents manufacturer engaged in the research, development, production, and focus on clinical testing for infectious diseases, such as Hepatitis virus, Noro virus, Parvo virus test kits, our products include rapid test cassette and Elisa kits.

All our products have been registered in National Medical Products Administration of China, in year 2020 we get Certificate of ISO 13485:2016 – QUALITY MANAGEMENT SYSTEMS FOR MEDICAL DEVICES from SGS. More importantly, we have awarded the registration certificate from National Medical Products Administration for Diagnostic Kit for IgM Antibody to COVID-19 and IgG antibody to COVID-19 during the outbreak in China, and also we developed COVID-19 Antigen test ; Neutralizing Antibody Test, these products selling well all overthe world