Ikhithi yokuxilonga ye-P24 Antigen ukuya kwi-Human Immunodeficiency Virus

inkcazo emfutshane:

I-P24 Antigen ukuya kwi-Human Immunodeficiency Virus

(Uvavanyo lwe-Fluorescence Immunochromatomatographic)

 


  • Ixesha lovavanyo:imizuzu eli-10-15
  • Ixesha Elisebenzayo:Iinyanga ezingama-24
  • Ukuchaneka:Ngaphezulu kwe-99%
  • Inkcazo:Uvavanyo/ibhokisi eyi-1/25
  • Ubushushu bokugcina:2℃ -30℃
  • Indlela yokusebenza:(Uvavanyo lwe-Fluorescence Immunochromatomatographic)
  • Iinkcukacha zeMveliso

    Iithegi zeMveliso

    Ikhithi yokuxilonga ye-P24 Antigen ukuya kwi-Human Immunodeficiency Virus

    (Uvavanyo lwe-Fluorescence Immunochromatomatographic)

    Ulwazi lwemveliso

    Inombolo yoMzekelo P24 Ukupakisha Iimvavanyo ezingama-25/ikhithi, iikhithi ezingama-30/i-CTN
    Igama Ikhithi yokuxilonga ye-P24 Antigen ukuya kwi-Human Immunodeficiency Virus
    Iisixhobo somculoudidi lwe-t Iklasi yesi-3
    Iimbonakalo Uvakalelo oluphezulu, Ukusebenza lula Isatifikethi I-CE/I-ISO13485
    Ukuchaneka > 99% Beka ubomi kwishelufa Iminyaka emibini
    Indlela yokusebenza (Uvavanyo lwe-Fluorescence Immunochromatomatographic) Inkonzo ye-OEM/ODM Iyafumaneka

     

    Inkqubo yovavanyo

    1 Vula iphakheji ye-reagent yebhegi yefoyile ye-aluminiyam, uze ukhuphe isixhobo sovavanyo;
    2 Faka isixhobo sovavanyo ngokuthe tye kwindawo yokuhlaziya umzimba;
    3 Kwiphepha lasekhaya le-interface yokusebenza ye-immune analyzer, cofa u-“Standard” ukuze ufake i-interface yovavanyo;
    4 Cofa u-“QC Scan” ukuze uskene ikhowudi ye-QR kwicala langaphakathi lekhithi; iiparameter ezinxulumene nekhithi yokufaka kwisixhobo, kwaye ukhethe uhlobo lwesampulu;
    5 Jonga ukuhambelana kwe-“Product Name”, “Batch Number” njl. njl. kwi-interface yovavanyo ngolwazi olukwileyibhile yekhithi;
    6 Emva kokuba ulwazi luqinisekisiwe, khupha izinto zokucoca isampuli, yongeza i-80µL yesampuli yeserum, uze uyixube ngokwaneleyo;
    7 Yongeza i-80µL yesisombululo esixutyiweyo esingentla kumngxuma wesampulu yesixhobo sovavanyo;
    8 Emva kokongeza isampuli epheleleyo, cofa u-“Timing” kwaye ixesha eliseleyo lovavanyo liza kuboniswa ngokuzenzekelayo kwi-interface.
    9 I-immune analyzer iza kugqiba uvavanyo kunye nohlalutyo ngokuzenzekelayo xa ixesha lovavanyo lifikile.

     

    Injongo Yokusebenzisa

    Le khithi ifanelekile kwi-in vitroubungakananiukufunyanwa kwe-antigen ye-human immunodeficiency virus (p24) kwisampuli ye-serum yomntu njengoncedo ekuxilongweni kosulelo lwe-human immunodeficiency virus. Le khithi inika iziphumo zokufunyanwa kwe-human immunodeficiency virus antigen (p24) kuphela kwaye iziphumo ezifunyenweyo ziya kuhlaziywa kunye nolunye ulwazi lweklinikhi.

    Uvavanyo lwe-P24 Antigen

    Isishwankathelo

    I-Human Immunodeficiency Virus (HIV) ikwi-genus Lentivirus kusapho lweRetroviridae kwaye yimbangela ye-Acquired Immunodeficiency Syndrome (AIDS), ehlulwe ngohlobo 1 kunye nohlobo 2 kuxhomekeke kwimvelaphi yemfuza yentsholongwane. Uhlobo 1 kunye nohlobo 2 zihlulwe ngokwemvelaphi yemfuza yentsholongwane. Iindlela eziphambili zokudlulisela intsholongwane yi-HIV kukudlulisela ngesondo, ukudluliselwa kwegazi kunye nokudluliselwa komntwana ngumama. Kwiiveki ezi-1-2 emva kosulelo lwe-HIV, uphawu lokuqala lwentsholongwane egazini yiproteni ephambili ye-p24.

     

    Uphawu:

    • Uvakalelo oluphezulu

    • ukufundwa kweziphumo kwimizuzu eli-15

    • Ukusebenza okulula

    • Ixabiso elithe ngqo lefektri

    • Andidingi matshini wongezelelweyo ukuze ndifunde iziphumo

     

    Uvavanyo lwe-P24 Antigen

    Ukusebenza kweklinikhi

    Uvavanyo lweklinikhi lokusebenza kwemveliso luvavanywa ngokuqokelela330 iisampulu zeklinikhi. Ikhithi ehambelanayo yendlela ye-electrochemiluminescence edwelisiweyo isetyenziswa njenge-reagent yokulawula. Iziphumo zovavanyo ziyathelekiswa, kwaye ukuthelekiswa kwazo kufundwa nge-linearity regression. Ii-coefficients zokunxibelelana kwezi vavanyo zimbini zeziY=0998X+0.380 kunye ne-R=0.9889, ngokulandelelana.

    Uvavanyo olukhawulezayo lwe-P24

    Ungathanda kwakhona:

    I-HCV

    Ikhithi yoVavanyo oluKhawulezayo lwe-HCV yeNyathelo elinye Ikhithi yoVavanyo oluKhawulezayo lwe-Hepatitis C Virus Antibody

     

    I-Hp-Ag

    Ikhithi yokuxilonga ye-Antigen ukuya kwi-Helicobacter Pylori (HP-AG) ene-CE evunyiweyo

    VD

    Ikhithi yovavanyo lwe-Diagnostic 25-(OH)VD Ikhithi yoVavanyo lwe-Quantitative Kit POCT Reagent


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