Izifo Ezidluliselwa Ngesondo
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Trichomonas Vaginalis Nucleic Acid Detection Kit (Fluorescence PCR)
Le khithi isetyenziselwa ukufunyaniswa komgangatho we-Trichomonas vaginalis nucleic acid kwiisampulu zemfihlo ye-urogenital yabantu.
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I-Ureaplasma Urealyticum Nucleic Acid Detection Kit (Fluorescence PCR)
Le khithi ifanelekile ukufunyaniswa komgangatho we-Ureaplasma urealyticum (UU) kwi-urinary tract yamadoda kunye neesampuli ze-secretion secretion yabasetyhini kwi-vitro.
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I-Herpes Simplex Virus Type 2 Nucleic Acid Detection Kit (Isothermal Amplification)
Le kit isetyenziselwa ubhaqo qualitative of herpes simplex virus uhlobo 2 nucleic acid kwiisampulu iphecana genitourinary in vitro.
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STD Multiplex Detection Kit (Fluorescence PCR)
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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I-Neisseria Gonorrhoeae ye-Nucleic Acid Detection Kit (Fluorescence PCR)
I-Gonorrhea sisifo esiqhelekileyo sokwabelana ngesondo esibangelwa usulelo lwe-Neisseria gonorrhoeae (NG)
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I-Herpes Simplex Virus Type 2 Nucleic Acid Detection Kit (Fluorescence PCR)
I-Herpes Simplex Virus Type 2 (HSV2) yintsholongwane ejikelezayo eyenziwe nge-tegument, i-capsid, i-core, kunye nemvulophu, kwaye iqulethe i-DNA enemigca emibini.
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Chlamydia Trachomatis Nucleic Acid Detection Kit (Fluorescence PCR)
I-Chlamydia trachomatis (CT) luhlobo lwe-microorganism ye-prokaryotic ene-parasitic ngokungqongqo kwiiseli ze-eukaryotic.
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Ureaplasma Urealyticum Nucleic Acid Detection Kit (Isothermal Amplification)
Le kit isetyenziselwa ukufumanisa umgangatho we-ureaplasma urealyticum nucleic acid kwiisampuli ze-genitourinary tract in vitro.
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I-Neisseria Gonorrhoeae Nucleic Acid Detection Kit (Isothermal Amplification)
Le khithi isetyenziselwa ukukhangela umgangatho we-Neisseria gonorrhoeae nucleic acid kwiisampuli ze-genitourinary tract in vitro.
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Chlamydia Trachomatis, Ureaplasma Urealyticum kunye neNeisseria Gonorrhoeae Nucleic Acid Detection Kit (Fluorescence PCR)
Le khithi ifanelekile ukufumanisa umgangatho wezifo eziqhelekileyo kwizifo ze-urogenital kwi-vitro, kuquka i-Chlamydia trachomatis (CT), i-Ureaplasma urealyticum (UU), kunye ne-Neisseria gonorrhoeae (NG).
