Syphilis TP Ab Test Cassette
ATR019-1
Antonmed Syphilis (TP) Ab Test Cassette is a rapid immunochromatographic test designed for the qualitative detection of antibodies to Treponema pallidum in human specimens.
Delivery:
EXW, FOB, DDP
minimum order:
200 pieces
Supply Ability:
1000000pieces / Month
Country of Origin:
China
Stock Time:
7Day
Quantity:
Introduction
Antonmed Syphilis (TP) Ab Test Cassette is a rapid immunochromatographic test designed for the qualitative detection of antibodies to Treponema pallidum in human specimens.
The cassette format combines a designated sample well with an integrated result window, providing a practical testing solution without the need for dedicated laboratory equipment. It can be incorporated into rapid diagnostic testing programs, clinical screening workflows, healthcare product portfolios and OEM/private-label IVD programs, subject to the applicable regulatory requirements of the target market.
The cassette format combines a designated sample well with an integrated result window, providing a practical testing solution without the need for dedicated laboratory equipment. It can be incorporated into rapid diagnostic testing programs, clinical screening workflows, healthcare product portfolios and OEM/private-label IVD programs, subject to the applicable regulatory requirements of the target market.
Key Features
TP Antibody Detection – Designed to qualitatively detect antibodies associated with Treponema pallidum infection.
Rapid Immunochromatographic Format – Uses lateral flow technology for convenient rapid testing.
Simple Cassette Design – Integrated sample well and result window support straightforward operation.
Visual Result Interpretation – Control and test lines provide an easy-to-read format.
No Dedicated Analyzer Required – Designed for visual interpretation according to the product's Instructions for Use.
Individual Packaging – Foil pouch packaging supports individual storage and distribution.
Flexible Specimen Options – Specimen type depends on the validated Antonmed product configuration.
OEM & Private Label Support – Branding, packaging and labeling can be customized for qualified customers.
TP Antibody Detection – Designed to qualitatively detect antibodies associated with Treponema pallidum infection.
Rapid Immunochromatographic Format – Uses lateral flow technology for convenient rapid testing.
Simple Cassette Design – Integrated sample well and result window support straightforward operation.
Visual Result Interpretation – Control and test lines provide an easy-to-read format.
No Dedicated Analyzer Required – Designed for visual interpretation according to the product's Instructions for Use.
Individual Packaging – Foil pouch packaging supports individual storage and distribution.
Flexible Specimen Options – Specimen type depends on the validated Antonmed product configuration.
OEM & Private Label Support – Branding, packaging and labeling can be customized for qualified customers.
How Does the Syphilis (TP) Ab Test Work?
The test is based on a lateral flow immunochromatographic assay. When the specimen is added to the sample well, it migrates through the test membrane by capillary action.
If antibodies to Treponema pallidum are present in the specimen, they interact with the test reagents and produce a visible line in the test region.
The control line functions as an internal procedural control and indicates that the test has operated correctly and that the specimen has migrated through the test device.
The exact antibodies, antigens, specimen volume and assay configuration should be described according to the validated Antonmed product documentation.
The test is based on a lateral flow immunochromatographic assay. When the specimen is added to the sample well, it migrates through the test membrane by capillary action.
If antibodies to Treponema pallidum are present in the specimen, they interact with the test reagents and produce a visible line in the test region.
The control line functions as an internal procedural control and indicates that the test has operated correctly and that the specimen has migrated through the test device.
The exact antibodies, antigens, specimen volume and assay configuration should be described according to the validated Antonmed product documentation.
