Chlamydia Nucleic Acid Detection Kit (fluorescent PCR Method) Rapid Test Kit

• Package: Not Customized
• Transport Package: Carton
• Specification: 58*33*36cm
• Trademark: Runmei
• Origin: China
• Production Capacity: 1000000kits/Month

Product Description

Chlamydia Nucleic Acid Detection Kit(Fluorescent PCR Method) 

 

Composition:	PCR Reaction Solution, Enzyme Mixture, Negative Control, Positive Control.
Applicable instrument:	This kit is suitable for ABI series, Bio-Rad series, Agilent Stratagene MX series, Roche LightCycler R480, Cepheid SmartCycler, Rotor-Gene series and other multi-channel real-time quantitative PCR instruments.
Intended Use:	This kit is used for the detection of Malaria Nucleic Acid and assisted diagnosis and epidemiological  surveillance of Monkeypox.
Package Specifications:	50 tests/kit & 200 tests/box.
Storage temperature:	-20 ± 5ºC.
Period of validity:	12 Months.
Product Features:	1.Accuracy-The limit of detection is 100 copies/ml and the specificity is 100%. 2.Flexible- Skin lesion material, including swabs of lesion surface and/or exudate, roofs from more than one lesion, or lesion crusts. Swab the lesion vigorously, to ensure adequate viral DNA is collected. 3.Simple-Simple operation,easy to. 4.Use Fast-Results within 40 min.

Interpretation of results:

1.If the test sample yields a typical S-type amplification curve in the FAM channel and the Ct value is ≤35, the sample can be judged to be Chlamydia positive.

2.If the test sample does not yield amplification curve or Ct value> 38 in the FAM channel, the sample can be judged to be Chlamydia negative.

3.If the test sample yields a Ct value range is 35-38 inthe FAM channel, the results need to retest. If the results repeated are consistent, and has a typical S-tyype amplification curve, the sample can be judged as Chlamydia positive,otherwise,the sample can bejudged as Chlamydia negative.