Imikhiqizo
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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-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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I-Enterovirus Universal, EV71 kanye ne-CoxA16
Le kit isetshenziselwa ukutholwa kwe-in vitro qualitative ye-enterovirus, i-EV71 ne-CoxA16 nucleic acid kuma-swabs womphimbo kanye namasampula oketshezi lwe-herpes eziguli ezinesifo somlomo we-hand-foot, futhi inikeza izindlela ezisizayo zokuxilonga iziguli ezinesifo somlomo we-hand-foot.
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Ureaplasma Urealyticum Nucleic Acid
Le kit isetshenziselwa ukutholwa kwekhwalithi ye-ureaplasma urealyticum nucleic acid kumasampula epheshana le-genitourinary in vitro.
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I-Neisseria Gonorrhoeae Nucleic Acid
Le kit isetshenziselwa ukutholwa kwekhwalithi ye-Neisseria gonorrhoeae nucleic acid kumasampula epheshana le-genitourinary in vitro.
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I-Herpes Simplex Virus Type 2 Nucleic Acid
Le kit isetshenziselwa ukutholwa kwekhwalithi ye-herpes simplex virus uhlobo 2 lwe-nucleic acid ku-swab ye-urethral yabesilisa kanye namasampula womlomo wesibeletho wesifazane.
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I-Chlamydia Trachomatis Nucleic Acid
Le khithi isetshenziselwa ukutholwa kwekhwalithi ye-Chlamydia trachomatis nucleic acid emchameni wesilisa, i-swab ye-urethral yabesilisa, namasampula womlomo wesibeletho wesifazane.
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I-HCG
Umkhiqizo usetshenziselwa ukutholwa kwekhwalithi ye-in vitro yezinga le-HCG kumchamo womuntu.
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Izinhlobo eziyisithupha zamagciwane okuphefumula
Le khithi ingasetshenziswa ukuthola ngokufanelekile i-nucleic acid ye-SARS-CoV-2, igciwane lomkhuhlane A, igciwane lomkhuhlane B, i-adenovirus, i-mycoplasma pneumoniae kanye negciwane lokuphefumula le-sycytial in vitro.
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I-Plasmodium Falciparum Antigen
Le khithi ihloselwe ukutholwa kwekhwalithi ye-in vitro yama-antigen e-Plasmodium falciparum egazini lomuntu le-peripheral nasegazini le-venous. Ihloselwe ukuxilonga okuyisizayo kweziguli okusolwa ukuthi zinegciwane le-Plasmodium falciparum noma ukuhlolelwa izimo zikamalaleveva.
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I-COVID-19, Flu A & Flu B Combo Kit
Le kit isetshenziselwa ukutholwa kwe-in vitro qualitative ye-SARS-CoV-2, ama-antigens omkhuhlane A/ B, njengendlela yokuxilongwa kwe-SARS-CoV-2, igciwane lomkhuhlane A, kanye nokutheleleka ngegciwane lomkhuhlane B. Imiphumela yokuhlolwa ingeyenkomba yomtholampilo kuphela futhi ayikwazi ukusetshenziswa njengesisekelo sodwa sokuxilongwa.
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I-Mycobacterium Tuberculosis DNA
Le kit isetshenziselwa ukutholwa kwekhwalithi ye-in vitro yeziguli ezinezimpawu/izimpawu ezihlobene nesifo sofuba noma okuqinisekiswe ukuhlolwa kwe-X-ray kokutheleleka kwesifo sofuba se-mycobacterium kanye nezibonelo zesikhwehlela zeziguli ezidinga ukuxilongwa noma ukuhlonzwa okuhlukile kwe-mycobacterium tuberculosis.
