Ikhithi yokuxilonga ye-Antibody kuya ku-Human Immunodeficiency Virus HIV Colloidal Gold

incazelo emfushane:

Ikhithi yokuxilonga ye-Antibody kuya Kumuntu
I-Immunodeficiency Virus (igolide le-Colloidal)

 


  • Isikhathi sokuhlola:10-15 imizuzu
  • Isikhathi esivumelekile:Izinyanga ezingama-24
  • Ukunemba:Ngaphezu kuka-99%
  • Ukucaciswa:1/25 ukuhlolwa/ibhokisi
  • Izinga lokushisa lesitoreji :2℃-30℃
  • Indlela yokwenza:Igolide le-Colloidal
  • I-oda (MOQ):500Izivivinyo
  • Imininingwane Yomkhiqizo

    Omaka bomkhiqizo

    Ikhithi yokuxilonga ye-Antibody kuya ku-Human Immunodeficiency Virus (i-Colloidal Gold)

    Ulwazi lokukhiqiza

    Inombolo Yemodeli I-HIV Ukupakisha 25 Ukuhlolwa/ikhithi, 30kits/CTN
    Igama Ikhithi yokuxilonga ye-Antibody kuya ku-Human Immunodeficiency Virus (i-Colloidal Gold) Ukuhlukaniswa kwezinsimbi Ikilasi III
    Izici Ukuzwela okuphezulu, ukusebenza okulula Isitifiketi CE/ ISO13485
    Ukunemba > 99% Impilo yeshelufu Iminyaka Emibili
    Indlela yokwenza Igolide le-Colloidal Isevisi ye-OEM/ODM Iyatholakala

     

    Inqubo yokuhlola

    1 Khipha idivayisi yokuhlola esikhwameni se-aluminium foil, uyibeke phezu kwetafula eliyisicaba bese umaka kahle isampula.
    2 Ukuze uthole amasampula e-serum ne-plasma, thatha amaconsi ama-2 uwafake emthonjeni we-spiked;kodwa, uma isampula kuyisampula yegazi lonke, thatha amaconsi angu-2 uwangeze emthonjeni onama-spiked futhi udinga ukungeza iconsi elingu-1 lesampula le-diluent.
    3 Umphumela kufanele ufundwe phakathi nemizuzu eyi-15-20.Umphumela wokuhlolwa ngeke uvumeleke ngemva kwemizuzu engama-20.

    Ihlose Ukusebenzisa

    Le khithi ifanele ukutholwa kwe-in vitro qualitative yegciwane le-HIV (1/2) amasosha omzimba amasosha omzimba ku-serum yabantu/i-plasma/amasampula egazi lonke njengosizo ekuhlonzweni kwegciwane le-HIV (1/2) le-antibody.Le khithi inikeza imiphumela yokuhlolwa kwe-HIV kuphela futhi imiphumela etholiwe kufanele ihlaziywe ngokuhambisana nolunye ulwazi lomtholampilo.Ihloselwe ukusetshenziswa ochwepheshe bezokwelapha kuphela.

    I-HIV

    Isifinyezo

    I-AIDS, isho ukuthi i-Acquired Immunodeficiency Syndrome, isifo esithathelwanayo esingalapheki nesibulalayo esibangelwa i-Human Immunodeficiency Virus (HIV), esisakazwa ikakhulukazi ngocansi nokwabelana ngemijovo, nangokudluliselana kumama kuye enganeni nangokudlulisela igazi. .Igciwane lesandulela ngculaza liyi-retrovirus ehlasela futhi ibhubhise kancane kancane amasosha omzimba, ibangele ukwehla kwamasosha omzimba futhi yenze umzimba ube sengozini yokuthola izifo futhi ekugcineni ufe.Ukuhlolwa kwe-HIV kubalulekile ekuvimbeleni ukudluliswa kwe-HIV kanye nokwelashwa kwamasosha omzimba e-HIV.

     

    Isici:

    • Ukuzwela okuphezulu

    • umphumela wokufunda emizuzwini eyi-15

    • Ukusebenza okulula

    • Intengo eqondile yasefekthri

    • Awudingi umshini owengeziwe wokufunda imiphumela

     

    Ikhithi ye-HIV rapiddiagnosis
    umphumela wokuhlolwa

    Ukufundwa kwemiphumela

    Ukuhlolwa kwe-reagent ye-WIZ BIOTECH kuzoqhathaniswa ne-reagent yokulawula:

    Imiphumela ye-WIZ Umphumela wokuhlola wereferensi yesithenjwa
    Okuhle Okubi Ingqikithi
    Okuhle 83 2 85
    Okubi 1 454 455
    Ingqikithi 84 456 540

    Izinga lokuqondana okuhle:98.81% (95%CI 93.56%~99.79%)

    Izinga lokuqondana okubi: 99.56% (95%CI98.42%~99.88%)

    Isamba sezinga lokuqondana:99.44% (95%CI98.38%~99.81%)

    Ungase futhi uthande:

    I-HCV

    Ikhithi Yokuhlola Okusheshayo ye-HCV Isinyathelo esisodwa se-Hepatitis C Virus Antibody Rapid Test Kit

     

    Hp-Ag

    Ikhithi Yokuxilonga Ye-Antigen Iya ku-Helicobacter Pylori (HP-AG) Nge-CE Evunyiwe

    VD

    Ikhithi Yokuxilonga 25-(OH)VD TEST Kit Quantitative Kit POCT Reagent


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