Iimveliso
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Plasmodium Antigen
Le kiti yenzelwe ukufumanisa umgangatho we-in vitro kunye nokuchongwa kwePlasmodium falciparum (Pf), iPlasmodium vivax (Pv), iPlasmodium ovale (Po) okanye iPlasmodium malaria (Pm) kwigazi le-venous okanye igazi elijikelezayo labantu abaneempawu kunye neempawu zeprotozoa yemalariya. , enokunceda ekuxilongeni usulelo lwePlasmodium.
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I-STD Multiplex
Le kit ihloselwe ukufumanisa umgangatho wezifo eziqhelekileyo zentsholongwane ye-urogenital, kuquka i-Neisseria gonorrhoeae (NG), i-Chlamydia trachomatis (CT), i-Ureaplasma urealyticum (UU), i-Herpes Simplex Virus Type 1 (HSV1), i-Herpes Simplex Virus Type 2 (HSV2) , I-Mycoplasma hominis (Mh), i-Mycoplasma genitalium (Mg) kwi-urinary tract yamadoda kunye neesampuli ze-secretion secretion yabasetyhini.
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Hepatitis C Virus RNA Nucleic Acid
I-HCV Quantitative Real-Time PCR Kit yi-in vitro Nucleic Acid Test (NAT) yokukhangela kunye nokulinganisa inani le-Hepatitis C Virus (HCV) nucleic acids kwiplasma yegazi lomntu okanye iisampulu zeserum ngoncedo lweQuantitative Real-Time Polymerase Chain Reaction (qPCR). ) indlela.
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Hepatitis B Virus Genotyping
Le khithi isetyenziselwa ukufumanisa ukuchwetheza okusemgangathweni kohlobo lwe-B, uhlobo lwe-C kunye nohlobo lwe-D kwi-serum efanelekileyo / iisampulu ze-plasma ze-virus ye-hepatitis B (HBV)
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Hepatitis B Virus Nucleic Acid
Le khithi isetyenziselwa ukufumanisa i-in vitro quantitative ye-hepatitis B yentsholongwane ye-nucleic acid kwiisampulu zeserum yabantu.
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IPlasmodium Falciparum/Plasmodium Vivax Antigen
Le khithi ilungele ukufunyanwa kwe-in vitro qualitative ye-Plasmodium falciparum antigen kunye ne-Plasmodium vivax antigen kwigazi lomntu le-peripheral kunye negazi le-venous, kwaye ilungele ukuxilongwa kwezigulane ezikrokrelekayo zosulelo lwe-Plasmodium falciparum okanye ukuhlolwa kweemeko zemalariya.
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Chlamydia Trachomatis Nucleic Acid
Le khithi isetyenziselwa ukuchongwa okusemgangathweni kweChlamydia trachomatis nucleic acid kumchamo oyindoda, i-swab ye-urethral yamadoda, kunye neesampulu zomlomo wesibeleko zabasetyhini.
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I-Enterovirus Universal, i-EV71 kunye ne-CoxA16 Nucleic Acid
Le khithi isetyenziselwa ukukhangela umgangatho we-in vitro we-enterovirus, i-EV71 kunye ne-CoxA16 nucleic acids kwi-swabs yomqala kunye neesampuli ze-herpes zolwelo lwezigulane ezinesifo somlomo wezandla, kwaye ibonelela ngeendlela ezincedisayo zokuxilongwa kwezigulane ezinesandla sonyawo-umlomo. isifo.
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I-Chlamydia Trachomatis, i-Ureaplasma Urealyticum kunye neNeisseria Gonorrhoeae Nucleic Acid
Le khithi ifanelekile ukufunyanwa kwekhwalithi yezifo eziqhelekileyo kwizifo ze-urogenital kwi-vitro, kuquka i-Chlamydia trachomatis (CT), i-Ureaplasma urealyticum (UU), kunye ne-Neisseria gonorrhoeae (NG).
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Ureaplasma Urealyticum Nucleic Acid
Le khithi isetyenziselwa ukufumanisa umgangatho we-ureaplasma urealyticum nucleic acid kwiisampuli ze-genitourinary tract in vitro.
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Neisseria Gonorrhoeae Nucleic Acid
Le khithi isetyenziselwa ukufunyaniswa komgangatho we-Neisseria gonorrhoeae nucleic acid kwiisampuli ze-genitourinary tract in vitro.
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I-Herpes Simplex Virus Type 2 Nucleic Acid
Le khithi isetyenziselwa ukubhaqa okusemgangathweni kwentsholongwane ye-herpes simplex uhlobo lwe-2 nucleic acid kwi-swab ye-urethral eyindoda kunye neesampuli zomlomo wesibeleko.
