Nanjing Liming Bio-products Co., Ltd.

Veterinary Diagnostics

Featured products

REF 501080 Specification 20 Tests/Box
Detection principle Immunochromatographic assay Specimens Feces
Intended Use The StrongStep® Salmonella Antigen Rapid Test is a rapid visual immunoassay for the qualitative, presumptive detection of Salmonella typhimurium, Salmonella enteritidis, Salmonella choleraesuis in human fecal specimens. This kit is intended for use as an aid in the diagnosis of Salmonella infection.
 
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.
 
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.
 
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 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.
 
StrongStep System Device for SARS-CoV-2Antigen Rapid Test employs immunochromatography technobgy to detect the SARS-CoV-2 nucleocapsid antigen in human saliva. This test is single use only and intended for self-testing. It is recommended to use this test within 7 days of symptom onset. lt is supported by the dinical performance assessment.

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