Nanjing Liming Bio-products Co., Ltd.

Neisseria gonorrhoeae

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For the qualitative detection of Trichomonas and/or Candida and/or Gardnerella Vaginalis antigens from vaginal swabs or from the saline solution prepared when making wet mount from vaginal swabs. This kit is intended to be used as an aid in the diagnosis of Candida albicans and/or Trichomonas Vaginalis andlorGardnerella Vaginalis infection.
REF 500090 Specification 20 Tests/Box
Detection principle Immunochromatographic assay Specimens Female vaginal swab
Intended Use StrongStep® Strep B antigen Rapid Test is a rapid visual immunoassay for the qualitative presumptive detection of Group B Streptococcal antigen in female vaginal swab.
 
REF 502010 Specification 20 Tests/Box
Detection principle Immunochromatographic assay Specimens Whole Blood/Serum / Plasma
Intended Use StrongStep® H. pylori Antibody Rapid Test is a rapid visual immunoassay for the qualitative presumptive detection of specific IgM and IgG antibodies to Helicobacter pylori with human whole blood/serum/plasma as specimen.
 
REF 501010 Specification 20 Tests/Box
Detection principle Immunochromatographic assay Specimens Feces
Intended Use StrongStep® Rotavirus antigen Rapid Test is a rapid visual immunoassay for the qualitative, presumptive detection of rotavirus in human fecal specimens.
 
REF 500050 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 Neisseria gonorrhoeae/Chlamydia trachomatis antigens in male urethral and female cervical swab
 
REF 501050 Specification 20 Tests/Box
Detection principle Immunochromatographic assay Specimens Feces
Intended Use The StrongStep® Vibrio cholerae O1 Antigen Rapid Test Device  (Feces) is a rapid visual immunoassay for the qualitative, presumptive detection of Vibrio cholerae O1 in human fecal specimens. This kit is intended for use as an aid in the diagnosis of Vibrio cholerae O1 infection.
 
REF  500020 Specification  20 Tests/Box
Detection principle  Immunochromatographic assay Specimens  Cervical/urethra swab
Intended Use It is suitable for qualitative detection of gonorrhoea/chlamydia trachomatis antigens in cervical secretions of women and urethral samples of men in vitro in various medical institutions for auxiliary diagnosis of the above pathogen infection.
 

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