quantitative kit CEA quick test kit factory direct

inkcazelo emfutshane:

Inombolo yoMfanekiso CEA Ukupakisha Iimvavanyo ze-25 / ikiti, i-20kits / i-CTN
Igama I-Diagnostic Kit Carcino-embryonic antigen (i-Fluorescence Immuno Assay) Ukuhlelwa kwesixhobo Udidi II
Iimbonakalo Uvakalelo oluphezulu, ukusebenza ngokulula Isatifikethi CE/ ISO13485
Umzekelo ISerum, iPlasma 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

    3
    4-(4)
    4-(3)

    UMGAQO KUNYE NENKQUBO YOKUHLOLA FOB

    UMGAQO

    I-membrane yesixhobo sovavanyo igqunywe nge-anti-CEA ye-antibody kwindawo yovavanyo kunye ne-antibody ye-IgG yebhokhwe kwindawo yolawulo. Iphedi elayibhile iqatywe nge-fluorescence ebhalwe i-anti-CEA antibody kunye nomvundla we-IgG kwangaphambili. Xa uvavanyo lwesampulu eqinisekileyo, i-antigen ye-CEA kwisampulu idibanisa kunye ne-fluorescence ebhalwe i-anti-CEA antibody, kwaye yenze umxube wokugonyeka. Phantsi kwesenzo se-immunochromatography, ukuhamba okuntsonkothileyo kwicala lephepha elifunxayo, xa intsonkothe ​​iphumelele ummandla wovavanyo, idityaniswe ne-anti-CEA yokugquma i-antibody, yenza inqanaba elitsha le-complex.CEA linxibelelene kakuhle nesiginali ye-fluorescence, kunye noxinzelelo lwe-CEA. kwisampulu inokubonwa 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-80μL i-serum okanye isampuli yeplasma kwisampulu ye-diluent, 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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