The Multiplex Real time PCR Kit for HPV and 16/18 Typing used for in vitro qualitative detecting 15 high-risk HPVs (16、18、31、 33、35、39、45、51、52、53、56、58、59、66、68) in human cervical exfoliated cells, and can identify HPV16 and 18 types, which can be used for auxiliary diagnosis of cervical cancer.
Twenty-three HPVs Genotyping Kit is an in vitro nucleic acid amplification test for the detection of high-risk HPV (Type 6, 11, 16, 18, 26, 31, 33, 35, 39, 42, 43, 44, 45, 51, 52, 53, 56, 58, 59, 66, 68, 73, 82) present in exfoliated cells from females’ cervix. The test results can be used for identification of HPV genotypes.
Twenty-three HPVs Genotyping Kit is an in vitro nucleic acid amplification test for the detection of high-risk HPV (Type 6, 11, 16, 18, 26, 31, 33, 35, 39, 42, 43, 44, 45, 51, 52, 53, 56, 58, 59, 66, 68, 73, 82) present in exfoliated cells from females’ cervix. The test results can be used for identification of HPV genotypes.
Cervical cancer is caused by the continuous overexpression of the E6/E7 oncogenes from high-risk HPV virus types. HPV E6/E7 mRNA Genotyping kit targets oncogenic activity of the HPV virus by detecting E6/E7 mRNA. HPV E6/E7 mRNA Genotyping kit are designed for a true molecular HPV screening and triage testing strategy to support risk stratification of women infected with HPV.
This kit is used for in vitro qualitative nucleic acid detection of Mycobacterium tuberculosis (MTB) and Non-Tuberculous Mycobacteria (NTM) in sputum.
This kit is used for in vitro qualitative nucleic acid detection of Mycobacterium tuberculosis (MTB) and Non-Tuberculous Mycobacteria (NTM) in sputum.
The kit is used for in vitro qualitative detection of eight Viral Diarrhea virus kinds of the Group A rotavirus(RV-A)/Group B rotavirus (RV-B)/enterovirus(EV)/Adenovirus(AdV)/Norwalk Viruses I (NOV-GI)/Norwalk Viruses II (NOV-GII)/Astrovirus(AV)/Sapovirus (SV) in stool, throat swab, herpes fluid and other samples
This kit is used for in vitro qualitative nucleic acid detection of Plasmodium in blood, serum, tissue or insect-borne specimens.
This kit is used for in vitro qualitative nucleic acid detection of Plasmodium in blood, serum, tissue or insect-borne specimens.
This kit is used for in vitro qualitative nucleic acid detection of Zika virus (ZIKV), dengue virus (DENV), and chikungunya virus (CHIKV) simultaneously in respiratory specimens including blood, serum, tissue or mosquito - borne specimens.
This kit is used for in vitro qualitative nucleic acid detection of SARS-CoV-2, Influenza A, Influenza B and respiratory syncytial virus (RSV) simultaneously in respiratory specimens including oropharyngeal swabs and sputum, bronchoalveolar lavage fluid and nasopharyngeal swab.
This kit is used for in vitro qualitative nucleic acid detection of SARS-CoV-2, Influenza A, Influenza B and respiratory syncytial virus (RSV) simultaneously in respiratory specimens including oropharyngeal swabs and sputum, bronchoalveolar lavage fluid and nasopharyngeal swab.
The kit is designed for the direct detection and differentiation of sexually transmitted infections by real-time PCR in urogenital/endocervical swabs and urine samples. The bacteria in the panel are: Neisseria gonorrhoeae (NG), Ureaplasma Urealyticum (UU), Mycoplasma genitalium (MG), Ureaplasma parvum (UP), Mycoplasma hominis (MH) and Trichomonas vaginalis (TV).
The kit uses multiple fluorescent RT-PCR (TaqMan probe method) and premix technology, which can detect pathogens by directly adding nucleic acids.
The kit uses multiple fluorescent RT-PCR (TaqMan probe method) and premix technology, which can detect pathogens by directly adding nucleic acids.