Nanjing Liming Bio-products Co., Ltd.

Chlamydia trachomatis

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REF 501070 Specification 20 Tests/Box
Detection principle Immunochromatographic assay Specimens Feces
Intended Use The StrongStep® Vibrio cholerae O1/O139 Antigen Combo Rapid Test is a rapid visual immunoassay for the qualitative, presumptive detection of Vibrio cholerae O1 and/or O139 in human fecal specimens. This kit is intended for use as an aid in the diagnosis of Vibrio cholerae O1 and/or O139 infection.
 
REF 500030 Specification 20 Tests/Box
Detection principle Immunochromatographic assay Specimens Cervical/urethra swab
Intended Use The StrongStep® Candida albicans Antigen Rapid Test is an immunochromatographic assay that detects pathogen antigens directly from vaginal swabs.
 
REF 500160 Specification 20 Tests/Box
Detection principle Immunochromatographic assay Specimens Cervicovaginal secretions
Intended Use StrongStep® Fetal Fibronectin Rapid Test is a visually interpreted immunochromatographic test intended to be used for the qualitative detection of fetal fibronectin in cervicovaginal secretions.
REF 501040 Specification 20 Tests/Box
Detection principle Immunochromatographic assay Specimens Feces
Intended Use StrongStep® H. pylori Antigen Rapid Test is a rapid visual immunoassay for the qualitative, presumptive detection of Helicobacter pylori antigen with human fecal as specimen.
 
REF 500170 Specification 20 Tests/Box
Detection principle Immunochromatographic assay Specimens Vaginal discharge
Intended Use StrongStep® PROM rapid test is a visually interpreted, qualitative immunochromatographic test for detection of IGFBP-1 from amniotic fluid in vaginal secretions during pregnancy.
 
This is a rapid immuno-chromatographic assay for the simultaneous detection of IgM and IgG antibodies to SARS-CoV-2 virus in human whole blood, serum or plasma.
REF 500010 Specification 20 Tests/Box
Detection principle Immunochromatographic assay Specimens

Cervical/urethra swab

Intended Use This is a rapid lateral-flow immunoassay for the qualitative presumptive detection of Chlamydia trachomatis antigen in male urethral and female cervical swab.
 

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