The HPV Antigen Rapid Test is a serological, lateral flow chromatographic immunoassay for the qualitative detection of HPV L1 Capsid protein in female cervical swab specimens. It is intended to be used as an aid in the diagnosis of cervical pre-cancer and cancer including types 6, 11, 16, 18, 31, 33, 45, 52 and 58. The test only provides preliminary screening results but not critical diagnosis criteria. Any reactive specimen with the HPV Antigen Rapid Test must be analyzed and confirmed with alternative testing method(s) and clinical findings. The test is intended for healthcare professional use.

 

SUMMARY
Infection with human papillomavirus (HPV) is a leading cause of cancer among women worldwide with approximately 500,000 new cervical cancer cases and 250,000 deaths each year1 . Cervical cancer is caused by persistent infection with a group of carcinogenic HPV genotypes (HPV16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, and probably HPV68)2 . The importance of cervical cancer is accentuated by the relatively young average age at incidence and death.
Cervical cancer screening strategies have evolved from cytology-based to HPV-based3 . Following the identification of HPV as the cause of cervical cancer and the development of sensitive HPV tests, HPV-based screening permits the extension of screening intervals and increased impact per number of lifetime screens3 .
The HPV Antigen Rapid Test utilizes of specific monoclonal antibodies to qualitatively detect HPV L1 Capsid protein in female cervical swab specimen, the test can be performed without cumbersome laboratory equipment, and the results are available at 15 minutes.

Caution: It is recommended that specimens be processed as soon as possible after collection. If test is not performed immediately, the swab specimens should be placed in a dry transport tube for storage or transport. The swab may be stored for 4-6 hours at room temperature (15-30ºC) or refrigerated (2-8ºC) for 24 hours. Do not freeze. All specimens should be equilibrated to room temperature (15-30ºC) before testing.

Features of lateral flow cassette: 
All of lateral flow cassette are engineered and designed to control flow, present the correct pressure points, enable sample addition in a controlled fashion, and fit tightly together without warp. Our design meet the specifications for some of the most popular materials used in lateral flow assays, our off-the-shelf cassette accommodates most of lateral flow assay strip designs.
Application:
Lateral flow cassette are important part of rapid antigen test kit, which can be used in early diagnostic and detection of DOA, pregnancy, ovulation, and other diseases.
MOQ:
The minimum order quantity is negotiable, welcome to contact us with your specific requirements, such as the slot/strip size, dimension, quantity, color, etc.
Our service:
OEM&ODM, customize cassette model and logo printing are available
Any requirement or anything we can help, feel free to send messages to us, we will reply you ASAP and hope to build a long-term business relationship with you!

Times Medical is principally engaged in the manufacture and sale of medical devices and in vitro diagnostic reagents. It mainly involves medical equipments such as physical examination, diagnosis, reproduction, family medicine, gynecological examination, and medical analysis.
Diagnostics now covers 29 items such as early pregnancy, ovulation, infectious diseases, sexually transmitted diseases, AIDS, and gynecological diseases; family medicine covers blood pressure, blood sugar, blood lipid testing, Cooling Patch and Warm Patch; gynecological examinations include bacterial vaginitis testing equipment and supplies.