Chlamydia Trachomatis, Chlamydia Pneumoniae and Mycoplasma Pneumoniae Detection Kit

Cat. No.: UP-RCCM-50

[INTENDED USE]

Ultrassay Chlamydia Trachomatis, Chlamydia Pneumoniae and Mycoplasma Pneumoniae Detection Kit is intended to detect Chlamydia trachomatis (CT), Chlamydia pneumoniae (CP) and Mycoplasma pneumoniae (MP) in children’s sputum samples qualitatively.
Chlamydia pneumoniae can only infect human beings and has only one serotype till now. Chlamydia pneumoniae is easy to form persistent infection and repeated infection due to weak immunity, and can cause respiratory system diseases, such as pneumonia, pharyngitis, laryngitis, bronchitis, etc. People are generally susceptible to Chlamydia pneumonia infection. Mycoplasma pneumoniae cause mycoplasma pneumonia, upper respiratory tract infection, bronchitis, lung abscess, immune hemolytic anemia, meningitis, myocarditis, pericarditis, nephritis, community-acquired pneumonia and other diseases. Chlamydia trachomatis causes a variety of diseases, such as trachoma, human urogenital diseases, and also neonatal conjunctivitis, pneumonia, premature rupture of membranes, premature delivery, neonatal death, and jaundice through mother to child transmission.
The test is manually operated. Experimental personnel who perform this test should have received professional training in gene amplification or molecular biology diagnostics and be qualified for relevant experimental operations. There should be reasonable biosecurity precautions and protective procedures in the laboratories. The test should only be performed in laboratories that follow safety practices according to the applicable Biosafety Regulations in Microbiological and Biomedical Laboratories.
The results of this kit are only for aiding to diagnosis and shall not be used as the sole basis for diagnosis or exclusion.

[TEST PRINCIPLE]

This kit uses polymerase chain reaction (PCR) technology based on TaqMan fluorescent probe to detect ORF1ab gene of 2019-Novel Coronavirus, M1 gene or NS1 gene of Influenza Virus and F gene of RSV from specimens including Oropharyngeal swabs, sputum and Bronchoalveolar lavage fluid collected from the patients or suspected patients.

[ACCEPTABLE SPECIMENS]

Nasopharyngeal swab, oropharyngeal swabs, bronchoalveolar lavage fluid, saliva, sputum or fecal

[APPLICABLE EQUIPMENT]

Applicable to Ultrassay XP96/Mini 16 Real time qPCR system, ABI 7500 Real-Time PCR thermocycles, Bio-Rad CFX 96.