Product Main

Specifications

[Product Name]
The common name: Diagnostic kit for Chlamydia (Colloidal Gold)
The English name: Diagnostic kit for Chlamydia (Colloidal Gold)
[Packing Model Specification]Card Type
[Intended use]
This product is used for qualitative detection of the presence of chlamydia in female cervix and male urethra, and the clinical auxiliary diagnosis of chlamydia infection, and test results also need to be further confirmed by the clinician in connection with symptoms, signs and other test results.
[Detection Principle]
Chlamydia diagnostic kit uses highly specific antigen-antibody reaction and immune chromatography analysis techniques for the qualitative detection of whether clinical specimens contain chlamydia trachomatis antigen, and the kit contains chlamydia trachomatis antigen-specific antibodies, which are pre-fixed on the test area (T) on the membrane, and the corresponding antibodies on the quality control area (C). During the detection, the pyrolysis-off specimens on the cotton swab are titrated into the sampling wells (S) of the kit, and the specimens make a specific antibody reaction with the chlamydia trachomatis antigen of the pre-coated gold particles. Then, the mixture followed up with upward chromatography under capillary effect. If it is positive, gold-labeled Chlamydia will first bind with Chlamydia trachomatis antigen in the specimens in the chromatography process, then the bonder will be combined by specific antibody of Chlamydia trachomatis antigen, which is fixed on the membrane, and within the test area (T) there will appear a red band. If it is negative, there will no red band within the test area (T). Regardless of whether the Chlamydia trachomatis antigen exists in clinical samples, there will be a red band within the quality control area (C). The red band within the quality control area (C) is to determine whether there is sufficient sample, and whether the process of chromatography is in line with the normal standards, and at the same time it is used as the internal control standards of the agent.