Basic Info.
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.
