Nanjing Liming Bio-products Co., Ltd.

Neisseria gonorrhoeae

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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.
 
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 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 500150 Specification 20 Tests/Box
Detection principle Immunochromatographic assay Specimens Throat swab
Intended Use The StrongStep® Strep A Rapid Test Device is a rapid immunoassay for the qualitative detection of Group A Streptococcal (Group A Strep) antigen from throat swab specimens as an aid to the diagnosis of Group A Strep pharyngitis or for culture confirmation.
 
REF 500070 Specification 20 Tests/Box
Detection principle Immunochromatographic assay Specimens Mucocutaneous lesions swab
Intended Use StrongStep® HSV 1/2 antigen rapid test is a breakthrough advance in the diagnosis of HSV 1/2 for it is designated for qualitative detection of HSV antigen, which boasts of high sensitivity and specificity.
 
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  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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