Imikhiqizo Nezixazululo ze-Macro & Micro-Test

I-PCR ye-Fluorescence | I-Isothermal Amplification | I-Colloidal Gold Chromatography | I-Fluorescence Immunochromatography

Imikhiqizo

  • Ikhithi Yokuthola Ukuguquka Kwezakhi Zofuzo Ze-EGFR Yomuntu (i-PCR ye-Fluorescence)-RUO

    Ikhithi Yokuthola Ukuguquka Kwezakhi Zofuzo Ze-EGFR Yomuntu (i-PCR ye-Fluorescence)-RUO

    [Ikhodi Yomkhiqizo] HWTS- TM4008

    Incazelo emfushane

    Le khithi ihloselwe ukusetshenziswa kocwaningo kuphela (i-RUO) futhi isetshenziselwa ukuthola izinguquko ezijwayelekile kuma-exons 18-21 esakhini se-EGFR kumasampula e-DNA akhishwe ukuze kusetshenziswe ucwaningo.

    Ukusetshenziswa Kocwaningo Kuphela

  • Ikhithi Yokuthola I-Nucleic Acid (i-Fluorescence PCR)-RUO eyomisiwe ngeqhwa

    Ikhithi Yokuthola I-Nucleic Acid (i-Fluorescence PCR)-RUO eyomisiwe ngeqhwa

    [Ikhodi Yomkhiqizo] HWTS-FE4040

    Incazelo emfushane

    Leli khithi lisetshenziselwa ukuthola i-nucleic acid ye-denguevirus (DENV) kusampula yeseramu yesiguli okusolwa ukuthi inesifo ukuze kusizwe ekuxilongweni kweziguli ezine-Dengue fever. Imiphumela yokuhlolwa etholwe yikhithi iwukubhekisela emtholampilo kuphela. Ukuze kwenziwe ukuxilongwa kokugcina, ukuhlaziywa okuphelele kwesimo sesiguli kumele kwenziwe kanye nokubonakaliswa kwesiguli kanye nokunye okutholakele elabhorethri.

    Ukusetshenziswa Kocwaningo Kuphela

     

  • Izinhlobo ezingu-18 ze-Human Papilloma Virus eyingozi kakhulu (16/18 Typing) I-Nucleic Acid Detection Kit (i-Fluorescence PCR)

    Izinhlobo ezingu-18 ze-Human Papilloma Virus eyingozi kakhulu (16/18 Typing) I-Nucleic Acid Detection Kit (i-Fluorescence PCR)

    Ikhodi Yomkhiqizo

    I-HWTS-CC018B

    Ukuvunyelwa Komkhiqizo

    CE, TFDA

    Ukusetshenziswa Okuhlosiwe

    Le khithi ifanelekela ukutholwa kwezinhlobo ezingu-18 zamagciwane e-human papilloma (HPV) (HPV16, 18, 26, 31, 33, 35, 39, 45, 51, 52, 53, 56, 58, 59, 66, 68, 73, 82) ze-nucleic acid fragments kumasampula omchamo womuntu, amasampula e-cervical swab yabesifazane, amasampula e-vaginal swab yabesifazane kanye ne-HPV 16/18 typing.

  • HWTS-RT065A/B/C/D-COVID-19 /Flu A &B/ RSV/ADV Ag Ag Combo Rapid Test

    HWTS-RT065A/B/C/D-COVID-19 /Flu A &B/ RSV/ADV Ag Ag Combo Rapid Test

    Le khithi ihloselwe ukuthola ama-antigen e-SARS-CoV-2, igciwane lomkhuhlane A no-B, igciwane lokuphefumula elihambisana nokuxhumana, kanye ne-Adenovirus kumasampula okuhlolwa kwamakhala okuvela kubantu abasolwa ngokutheleleka zingakapheli izinsuku eziyi-7 kusukela ekuqaleni kwezimpawu kanye nokuxhumana okuseduze ekuxilongweni okuhlukile kokutheleleka kwendlela yokuphefumula yi-SARS-CoV-2, igciwane lomkhuhlane A no-B, igciwane lokuphefumula elihambisana nokuxhumana, kanye ne-Adenovirus. Imiphumela yokuhlolwa akufanele isetshenziswe njengesisekelo sodwa sesinqumo somtholampilo sokuxilongwa nokwelashwa. Ukuxilongwa okwengeziwe kwezokwelapha kufanele kuqinisekiswe ngezindlela zokuhlola ezihlukile kanye neminye imiphumela yezokwelapha. Le khithi ingeyokusetshenziswa kokuxilonga okusebenzisana nokuxhumana kuphela futhi ayizenzakalelayo.

  • Ikhithi Yokuthola Ubuningi Bokuthola I-Human BCR-ABL1 Fusion Gene (i-Fluorescence PCR)-RUO

    Ikhithi Yokuthola Ubuningi Bokuthola I-Human BCR-ABL1 Fusion Gene (i-Fluorescence PCR)-RUO

    Le khithi isetshenziselwa ukuthola inani lamazinga e-RNA yohlobo lwe-M, uhlobo lwe-m, kanye nohlobo lwe-μ lwe-BCR-ABL1 kumasampula ocwaningo lwethambo lomuntu kanye negazi eliphelele ukuze kusetshenziswe ucwaningo. Lo mkhiqizo uhloselwe ukusetshenziswa kocwaningo kuphela (RUO) futhi awuhloselwe ukusetshenziswa ekuxilongweni kwezokwelapha noma kwezinye izinhlelo zokusebenza zokuxilonga.

  • Ikhithi Yokuthola Izinguquko ze-KRAS 8 (i-Fluorescence PCR)-RUO

    Ikhithi Yokuthola Izinguquko ze-KRAS 8 (i-Fluorescence PCR)-RUO

    [Ikhodi Yomkhiqizo] HWTS-TM4009

    Incazelo emfushane

    Le khithi yenzelwe ukutholwa kwezinguquko ezingu-8 ezishintshashintshayo kuma-codon 12 no-13 e-K-ras gene ku-DNA ekhishwe ezingxenyeni ze-pathological ezifakwe i-paraffin yomuntu.

    Ukusetshenziswa Kocwaningo Kuphela

  • Izinhlobo Eziyisishiyagalolunye Zekhithi Yokuthola I-Nucleic Acid Yokutheleleka Kwe-genitourinary Tract Infection (i-Fluorescence PCR)

    Izinhlobo Eziyisishiyagalolunye Zekhithi Yokuthola I-Nucleic Acid Yokutheleleka Kwe-genitourinary Tract Infection (i-Fluorescence PCR)

    [Igama Lomkhiqizo]Izinhlobo Eziyisishiyagalolunye Zekhithi Yokuthola I-Nucleic Acid Yokutheleleka Kwe-genitourinary Tract Infection

    (I-PCR ye-Fluorescence)

    [UmkhiqizoIkhodi]I-HWTS-UR048

    [Ukusetshenziswa Okuhlosiwe]

    Le khithi ifaneleka ekutholakaleni kwe-Chlamydia trachomatis (CT) esezingeni eliphezulu ngaphakathi kwe-vitro,Neisseria gonorrhoeae (NG), Mycoplasma hominis (Mh), Herpes Simplex Virus Type1 (HSV1), i-Ureaplasma urealyticum, UU), i-Herpes Simplex Virus Type 2 (HSV2),Ureaplasma Parvum (UP), Mycoplasma genitalium (Mg), Trichomonal vaginitis (TV)emchameni, i-urethral swab yesilisa, i-cervical swab yesifazane, kanye namasampula e-vaginal swab yesifazane,ukuhlinzeka ngosizo ekuxilongweni nasekuphathweni kweziguli ezine-genitourinary tractukutheleleka.

  • Izinhlobo eziyi-17 ze-Human Papillomavirus (16/18/6/11/44 Ukuthayipha) Ikhithi Yokuthola I-Nucleic Acid (i-Fluorescence PCR) - Ukusetshenziswa Kocwaningo Kuphela

    Izinhlobo eziyi-17 ze-Human Papillomavirus (16/18/6/11/44 Ukuthayipha) Ikhithi Yokuthola I-Nucleic Acid (i-Fluorescence PCR) - Ukusetshenziswa Kocwaningo Kuphela

    Le khithi ifanelekela ukutholwa kwezinhlobo ezingu-17 ze-human papillomavirus (HPV 6, 11, 16, 18, 31, 33, 35, 39, 44, 45, 51, 52, 56, 58, 59, 66, 68) ze-nucleic acid fragments ezithile kusampula yomchamo, isampula ye-cervical swab yowesifazane kanye nesampula ye-vaginal swab yowesifazane, kanye nokutholwa kokuthayipha kwe-HPV 16/18/6/11/44.

  • HWTS-RT201A/B/C/D-RSV/ADV Ag Ukuhlolwa Okusheshayo

    HWTS-RT201A/B/C/D-RSV/ADV Ag Ukuhlolwa Okusheshayo

    Le khithi yenzelwe ukuthola ama-antigen e-Respiratory Syncytial Virus kanye ne-Adenovirus ngaphakathi kwe-vitro ngamasampula e-nasal swabs avela kubasolwa ngokutheleleka zingakapheli izinsuku eziyi-7 kusukela izimpawu ziqalile kanye nokuxhumana okuseduze ekuxilongweni okuhlukile kokutheleleka kwendlela yokuphefumula yi-Respiratory Syncytial Virus kanye ne-Adenovirus. Imiphumela yokuhlolwa akufanele isetshenziswe njengesisekelo sodwa sesinqumo somtholampilo sokuxilongwa nokwelashwa. Ukuxilongwa okwengeziwe kwezokwelapha kufanele kuqinisekiswe ngezindlela zokuhlola ezihlukile kanye neminye imiphumela yezokwelapha.

    Ikhithi yayiwukuhlolwa kwe-in vitro kuphela futhi ayizenzakalelayo.

  • Ikhithi Yokuthola I-Nucleic Acid ye-Bundybugyo Virus Ebola (i-Fluorescence PCR)

    Ikhithi Yokuthola I-Nucleic Acid ye-Bundybugyo Virus Ebola (i-Fluorescence PCR)

    [Igama Lomkhiqizo] Ikhithi Yokuthola I-Nucleic Acid ye-Bundybugyo Virus Ebola (i-Fluorescence PCR)

    [UmkhiqizoIkhodi] I-HWTS-FE4023

    [Incazelo emfushane] 

    Lo mkhiqizo wenzelwe ukuthola i-nucleic acid esezingeni eliphezulu ngaphakathi kwe-vitro

    Igciwane le-Bundybugyo Ebola egazini lomuntu lonke, i-serum/plasma, kanye namasampula e-Oral swab.

  • Ikhithi Yokuthola I-Human Leukocyte Antigen B27 Nucleic Acid (i-Fluorescence PCR)-RUO

    Ikhithi Yokuthola I-Human Leukocyte Antigen B27 Nucleic Acid (i-Fluorescence PCR)-RUO

    Ikhithi Yokuthola I-Human Leukocyte Antigen B27 Nucleic Acid (i-Fluorescence PCR)

     

    I-HWTS-GE011A

     

    Le khithi isetshenziselwa ukuthola i-DNA esezingeni eliphezulu kuma-antigen e-human leukocyte antigen i-HLA-B*2702, i-HLA-B*2704 kanye ne-HLA-B*2705.

  • Ukuhlolwa Okusheshayo kwe-HWTS-RT200A/B/C/D-COVID-19/ Flu A&B Ag

    Ukuhlolwa Okusheshayo kwe-HWTS-RT200A/B/C/D-COVID-19/ Flu A&B Ag

    Le khithi ihloselwe ukuthola ama-antigen e-SARS-CoV-2, igciwane lomkhuhlane A kanye no-B ngaphakathi kwe-vitro ngamasampula e-swabs yamakhala avela kubasolwa ngokutheleleka zingakapheli izinsuku eziyi-7 kusukela kuqale izimpawu kanye nokuxhumana okuseduze ekuxilongweni okuhlukile kokutheleleka kwendlela yokuphefumula yi-SARS-CoV-2, igciwane lomkhuhlane A kanye no-B. Imiphumela yokuhlolwa akufanele isetshenziswe njengesisekelo sodwa sesinqumo somtholampilo sokuxilongwa kanye nokwelashwa. Ukuxilongwa okwengeziwe kwezokwelapha kufanele kuqinisekiswe ngezindlela zokuhlola ezihlukile kanye neminye imiphumela yezokwelapha. Le khithi ingeyokuxilongwa kwe-in vitro kuphela futhi ayizenzakalelayo.