Syphilis Rapid Test
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INTENDED USE |
Syphilis Rapid Test (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Treponema Pallidum (TP) in whole blood, serum or plasma to aid in the diagnosis of Syphilis.
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SUMMARY |
Treponema Pallidum (TP) is the causative agent of the venereal disease Syphilis. TP is a spirochete bacterium with an outer envelope and a cytoplasmic membrane. Relatively little is known about the organism in comparison with other bacterial pathogens. According to the Center for Disease Control (CDC), the number of cases of Syphilis infection has markedly increased since 1985. Some key factors that have contributed to this rise include the crack cocaine epidemic and the high incidence of prostitution among drug users. One study reported a substantial epidemiological correlation between the acquisition and transmission of the HIV virus and Syphilis.
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PRINCIPLE |
Syphilis Rapid Test Device (Whole Blood/Serum/Plasma) is a qualitative membrane based immunoassay for the detection of TP antibodies (IgG and IgM) in whole blood, serum or plasma. In this test procedure, recombinant Syphilis antigen is immobilized in the test line region of the test. After specimen is added to the specimen well of the device, it reacts with Syphilis antigen coated particles in the test. This mixture migrates chromatographically along the length of the test and interacts with the immobilized Syphilis antigen.
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How to use |

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Packing Details |
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Syphilis Rapid Test |
SYP-W201 |
Test devices |
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Buffer |
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Disposable specimen droppers |
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Package insert |
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Delivery |

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Certification |

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FAQ |
Q: How does the company evaluate product quality?
A: We strictly follow ISO: 13485 KMS.
Technology advancement research and development specialist.
Professionals adhere to the code of conduct.
The department closely monitors the quality of the production and packaging process.
Q: What is the warranty?
A: Automotive certificate: 2 years.
Q: What is MOQ?
A: MOQ: 50 installations per meter, 100 boxes per test group.
Initially, an experimental method was used.
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