High Accuracy Gonorrhea Antigen Test Kit Gonorrhea Rapid Test Strip/Cassette

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Basic Info.

Product Description

Product Description

EVANCARE Diagnostic Gonorrhea Rapid Test Kits


For professional and in vitro diagnostic use only.

[INTENDED USE] The Gonorrhea Rapid Test Device(Swab)is used for qualitative detection of the presence of Gonorrhea in female cervix and male urethra, and the clinical auxiliary diagnosis of Gonorrhea infection, and test results also need to be further confirmed by the clinician in connection with symptoms, signs and other test results. [PRINCIPLE] The Gonorrhea Rapid Test Device(Swab)uses highly specific antigen-antibody reaction and immune chromatography analysis techniques for the qualitative detection of whether clinical specimens contain Gonorrhea trachomatis antigen, and the kit contains Gonorrhea 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 Gonorrhea 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 Gonorrhea will first bind with Gonorrhea trachomatis antigen in the specimens in the chromatography process, then the bonder will be combined by specific antibody of Gonorrhea trachomatis antigen, which is fixed on the membrane, and within the test samples, there will be a red band within the quality control area (C). The red band 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 Gonorrhea trachomatis antigen exists in clinical 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.
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Detailed Photos

Positive: *Two lines appear. One colored line should be in the control region (C), and another apparent colored line adjacent should be in the test region (T). Negative: One colored line appears in the control region (C). No line appears in the test region (T). Invalid: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test using a new test cassette. If the problem persists, discontinue using the lot immediately and contact your local distributor.

Company Profile

Certifications

Product Procedure

Activity Exhibition

FAQ