Ikhithi yokuxilonga Ubungakanani bekhithi ye-Hs-CRP yovavanyo oluchaneke kakhulu

inkcazelo emfutshane:

Inombolo yoMfanekiso Hs-CRP Ukupakisha Iimvavanyo ze-25 / ikiti, i-20kits / i-CTN
Igama I-Diagnostic Kit for Hypersensitive C-reactive protein (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-CRP ye-antibody kwindawo yovavanyo kunye ne-antibody ye-IgG yebhokhwe kwindawo yolawulo. Iphedi elayibhile iqatywe nge-fluorescence ebhalwe i-anti-CRP ye-antibody kunye nomvundla we-IgG kwangaphambili. Xa uvavanyo lwesampulu eqinisekileyo, i-antigen ye-CRP kwisampulu idibanisa ne-fluorescence ebhalwe i-anti-CRP ye-antibody, kwaye yenze umxube wokuzivikela komzimba. Phantsi kwesenzo se-immunochromatography, ukuhamba okuntsonkothileyo kwicala lephepha elifunxayo, xa i-complex iphumelele ummandla wovavanyo, idityaniswe ne-anti-CRP yokwambathisa i-antibody, yenza into entsha. Inqanaba le-CRP lihambelana ngokufanelekileyo kunye nomqondiso we-fluorescence, kwaye ukuxinwa kwe-CRP kwisampulu kunokubonwa nge-fluorescence immunoassay assay.

    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-5μL ye-serum / isampuli yeplasma (okanye i-10μL igazi elipheleleyo) kwisampulu yokuxutywa, kwaye udibanise kakuhle.
    7. Yongeza i-80μL yesisombululo sesampulu kwisampulu yequla lekhadi.
    8. Klikha iqhosha elithi "standard test", emva kwemizuzu emi-3, isixhobo siya kubona ngokuzenzekelayo ikhadi lovavanyo, sinokufunda iziphumo kwisikrini 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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