We created this page for medical staff.
*Read carefully the package insert before use.
Syphilis is a disease caused by the spirochete Treponema pallidum (Nichols strain, TP). Currently, two methods are available for serological testing for syphilis: a method using lipid antigens, such as cardiolipin (STS) and a method using TP antigens. As test results differ between these two methods depending on the stage, both are performed in conjunction to detect infection or to diagnose the disease state.
SEKISUI MEDICAL's "MEDIACE TPLA " and "MEDIACE RPR" are the world's first diagnostic reagents for syphilis on a fully automated system. These reagents are used to rapidly measure serum anti-TP antibodies and syphilitic antilipid antibodies using particles of artificial carrier latex with a measurement principle based on latex turbidimetry.
Treponema Antibody Kit MEDIACE TPLA
- Marketing Approval Number: 20900AMZ00373000
- Measurement unit: T.U. (TITER UNITS) is used for the reagent. 1280 T.U. corresponds to 1280 reciprocal titer of TPHA test
- 1 T.U. equals 2 mIU with WHO reference material
- *This package insert follows the Pharmaceuticals, Medical devices and Other Therapeutic Products Act of Japan.
|MEDIACE TPLA (A)||Sample Dilution Buffer||4×18mL||2-8℃|
|MEDIACE TPLA (M)||Sample Dilution Buffer||2×49mL||2-8℃|
|Standard Syphilis Positive Serum (A)*||Syphilis Positive Human Serum||1×5conc.×1mL||2-8℃|
- *Not an in vitro diagnostic product in Japan.
"MEDIACE" is a trademark or registered trademark of SEKISUI MEDICAL CO., LTD. in Japan and/or other countries.
- Clinical Chemistry
We prepared this page for medical staff (doctors, dentists, pharmacists, clinical laboratory technicians, nurses, etc.) in Japan to ensure the correct use of our products. You should be aware that the information provided is not intended for overseas medical staff and the general public.