Ikhithi yovavanyo olukhawulezayo lwe-HCV inyathelo elinye i-Hepatitis C Virus Antibody quick test kit

inkcazelo emfutshane:

Inombolo yoMfanekiso HCV Ukupakisha 25 Iimvavanyo/ikhithi
Igama Diagnostic Kit Hepatitis C Virus Antibody Ukuhlelwa kwesixhobo Udidi II
Iimbonakalo Uvakalelo oluphezulu Isatifikethi CE/ ISO13485
Umzekelo ilindle Beka ubomi kwishelufa Iminyaka emibini
Ukuchaneka > 99% Iteknoloji Ikhithi yobungakanani
Ugcino 2′C-30′C Uhlobo Izixhobo zokuHlalutya kwePathological


  • Ixesha lovavanyo:Imizuzu eyi-10-15
  • Ixesha elisebenzayo:Iinyanga ezingama-24
  • Ukuchaneka:Ngaphezulu kwe-99%
  • Inkcazo:1/25 uvavanyo / ibhokisi
  • Ubushushu bokugcina :2℃-30℃
  • Iinkcukacha zeMveliso

    Iithegi zeMveliso

    IiParameters zeeMveliso

    3Hba1c
    4-(3)
    4-(4)

    UMGAQO KUNYE NENKQUBO YOKUHLOLA FOB

    UMGAQO

    Inwebu yesixhobo sovavanyo igqunywe nge-antigen ye-HCV kwindawo yovavanyo kunye ne-antibody ye-IgG yebhokhwe kwindawo yolawulo. Iphedi elayibhile iqatywe nge-fluorescence ebhalwe i-HCV antigen kunye ne-Rabbit IgG kwangaphambili. Xa uvavanya isampulu eqinisekileyo, i-antibody ye-HCV kwisampulu idibanisa ne-fluorescence ebhalwe i-antigen ye-HCV, kwaye yenze umxube wokuzivikela komzimba. Phantsi kwesenzo se-immunochromatography, ukuhamba okuntsonkothileyo kwicala lephepha elifunxayo, xa intsonkothe ​​iphumelele ummandla wovavanyo, idityaniswe ne-HCV antigen coating antigen, yenza inqanaba elitsha le-antibody. I-antibody ye-HCV kwisampulu inokufunyanwa ngovavanyo lwe-fluorescence immunoassay

    Inkqubo yoVavanyo:

    Nceda ufunde incwadi yokusebenza kwesixhobo kunye nokufakwa kwephakheji phambi kovavanyo.

    1. Beka eceleni zonke ii-reagents kunye neesampuli kwiqondo lokushisa.
    2. Vula i-Portable Immune Analyzer (WIZ-A101), faka igama lokungena kwi-akhawunti ngokwendlela yokusebenza kwesixhobo, kwaye faka ujongano lokubona.
    3. Skena ikhowudi yokuchaza ukuze uqinisekise into yovavanyo.
    4. Khupha ikhadi lovavanyo kwibhegi yefoyile.
    5. Faka ikhadi lovavanyo kwi-slot yekhadi, skena ikhowudi ye-QR, kwaye unqume into yovavanyo.
    6. Yongeza i-10μL serum okanye isampulu yeplasma kwisampulu yokuxutywa, kwaye udibanise kakuhle.
    7. Yongeza i-80μL yesisombululo sesampulu kwisampulu yequla lekhadi.
    8. Klikha iqhosha elithi "standard test", emva kwemizuzu eyi-15, isixhobo siya kubona ngokuzenzekelayo ikhadi lovavanyo, singakwazi ukufunda iziphumo kwiscreen sokubonisa sesixhobo, kwaye sirekhode/siprinte iziphumo zovavanyo.
    9. Jonga kumyalelo we-Portable Immune Analyzer (WIZ-A101).

    ukupakisha

    Ngathi

    贝尔森主图_conew1

    I-Xiamen Baysen Medical Tech limited lishishini eliphakamileyo lebhayoloji elizinikele ekufakeni i-reagent yokuxilonga ngokukhawuleza kwaye idibanise uphando kunye nophuhliso, imveliso kunye nokuthengisa kuyo yonke. Kukho uninzi lwabasebenzi bophando oluphambili kunye nabaphathi beentengiso kwinkampani, bonke banamava atyebileyo okusebenza eChina nakwishishini lamazwe ngamazwe le-biopharmaceutical.

    Umboniso wesatifikethi

    dxgrd

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