Nanjing Liming Bio-products Co., Ltd.

SARS-CoV-2 IgM/IgG Antibody Rapid Test

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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 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  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.
 
REF 501100 Specification 20 Tests/Box
Detection principle Immunochromatographic assay Specimens Feces
Intended Use StrongStep® Giardia lamblia Antigen Rapid Test Device (Feces) is a rapid visual immunoassay for the qualitative, presumptive detection of Giardia lamblia in human fecal specimens. This kit is intended for use as an aid in the diagnosis of Giardia lamblia infection.
 
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 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.
 
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.

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