Imikhiqizo
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I-Helicobacter Pylori Antibody
Le kit isetshenziselwa ukutholwa kwekhwalithi ye-in vitro yamasosha omzimba e-Helicobacter pylori ku-serum yomuntu, i-plasma, igazi eligcwele le-venous noma amasampula egazi agcwele umunwe, futhi inikeze isisekelo sokuxilongwa okuyisizayo kokutheleleka nge-Helicobacter pylori ezigulini ezinezifo zesisu.
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Isampula yokukhishwa kwe-Reagent
Ikhithi iyasebenza ekwelashweni kwangaphambili kwesampula okufanele ihlolwe, ukuze kube lula ukusetshenziswa kwama-in vitro diagnostic reagents noma amathuluzi okuhlola umhlaziyi.
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Izinhlobo ezingama-28 ze-HPV Nucleic Acid
Ikhithi isetshenziselwa ukutholwa kwe-in vitro qualitative yezinhlobo ezingama-28 ze-human papillomaviruses (HPV6, 11, 16, 18, 26, 31, 33, 35, 39, 40, 42, 43, 44, 45, 51, 52, 53 , 54, 56, 58, 59, 61, 66, 68, 73, 81, 82, 83) i-nucleic acid kumchamo wesilisa/ wesifazane kanye namaseli akhishwe wesibeletho sowesifazane, kodwa igciwane alikwazi ukuthayipha ngokuphelele.
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I-Plasmodium Antigen
Le khithi ihloselwe ukuhlonza ikhwalithi ye-in vitro kanye nokuhlonza i-Plasmodium falciparum (Pf), i-Plasmodium vivax (Pv), i-Plasmodium ovale (Po) noma i-Plasmodium malaria (Pm) egazini le-venous noma egazini le-peripheral labantu abanezimpawu nezimpawu ze-protozoa kamalaleveva. , engasiza ekuxilongeni ukutheleleka nge-Plasmodium.
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I-STD Multiplex
Le kit ihloselwe ukutholwa kwekhwalithi yamagciwane avamile wezifo ze-urogenital, okuhlanganisa 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) ku-urinary tract wesilisa kanye namasampula okukhishwa kwepheshana lobulili besifazane.
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I-Hepatitis C Virus RNA Nucleic Acid
I-HCV Quantitative Real-Time PCR Kit iyi-in vitro Nucleic Acid Test (NAT) ukuze ithole futhi ilinganise ama-nucleic acid e-Hepatitis C Virus (HCV) ku-plasma yegazi lomuntu noma amasampula e-serum ngosizo lwe-Quantitative Real-Time Polymerase Chain Reaction (qPCR ) indlela.
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I-Hepatitis B Virus Genotyping
Le khithi isetshenziselwa ukutholwa kokuthayipha kwekhwalithi yohlobo B, uhlobo C kanye nohlobo D kumasampula e-serum/plasma egciwane le-hepatitis B (HBV)
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I-Hepatitis B Virus Nucleic Acid
Le kit isetshenziselwa ukutholwa kwe-in vitro quantitative ye-hepatitis B virus nucleic acid kumasampula e-serum yomuntu.
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I-Plasmodium Falciparum/Plasmodium Vivax Antigen
Le kit ifanele ukutholwa kwekhwalithi ye-in vitro ye-Plasmodium falciparum antigen kanye ne-Plasmodium vivax antigen egazini lomuntu eliseceleni kwe-venous kanye ne-venous blood, futhi ilungele ukuxilonga iziguli okusolwa ukuthi zinegciwane le-Plasmodium falciparum noma ukuhlolelwa izimo zikamalaleveva.
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I-Enterovirus Universal, EV71 kanye ne-CoxA16 Nucleic Acid
Le kit isetshenziselwa ukutholwa kwe-in vitro qualitative ye-enterovirus, i-EV71 kanye ne-CoxA16 nucleic acid ku-swabs yomphimbo kanye namasampula oketshezi lwe-herpes eziguli ezinesifo somlomo we-hand-foot, futhi inikeza izindlela ezisizayo zokuxilonga iziguli ezine-hand-foot-mouth. isifo.
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I-Chlamydia Trachomatis, i-Ureaplasma Urealyticum ne-Neisseria Gonorrhoeae Nucleic Acid
Le kit ifanele ukutholwa kwekhwalithi yamagciwane avamile ezifweni ze-urogenital in vitro, okuhlanganisa i-Chlamydia trachomatis (CT), i-Ureaplasma urealyticum (UU), ne-Neisseria gonorrhoeae (NG).
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Ureaplasma Urealyticum Nucleic Acid
Le kit isetshenziselwa ukutholwa kwekhwalithi ye-ureaplasma urealyticum nucleic acid kumasampula epheshana le-genitourinary in vitro.
