I-C-creactive protein ye-CRP ikhithi yokuvavanya ngokukhawuleza

inkcazelo emfutshane:

I-Diagnostic Kit ye-C-reactive Protein

 

 


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

    Iithegi zeMveliso

    Diagnostic Kit for Cardiac Troponin I ∕Isoenzyme MB ye Creatine Kinase ∕Myoglobin

    Indlela yokusebenza:Fluorescence Immunochromatographic Assay

    Ulwazi lwemveliso

    Inombolo yoMfanekiso CRP Ukupakisha Iimvavanyo ze-25 / ikiti, i-30kits / i-CTN
    Igama I-Diagnostic Kit ye-C-creative protein Ukuhlelwa kwesixhobo Iklasi I
    Iimbonakalo Uvakalelo oluphezulu, ukusebenza ngokulula Isatifikethi CE/ ISO13485
    Ukuchaneka > 99% Beka ubomi kwishelufa Iminyaka emibini
    Indlela yokusebenza Fluorescence Immunochromatographic Assay Inkonzo ye-OEM/ODM Iyafumaneka

     

    UKUSETYENZISWA OKUHLOSIWEYO

    Le kit iyasebenza kwi-vitro quantitative discovery ye-C-reactive protein (CRP) kwi-serum yabantu / i-plasma / iisampulu zegazi elipheleleyo, ukuxilongwa kwe-acute and chronic inflammation okanye usulelo. Oku
    ikiti ibonelela kuphela isiphumo sovavanyo lweprotheyini ye-C-reactive, kwaye umphumo ofunyenweyo uya kuhlalutywa ngokudibanisa nolunye ulwazi lwekliniki.

    Inkqubo yovavanyo

    1 Ngaphambi kokusebenzisa i-reagent, funda iphakheji efakwe ngononophelo kwaye uziqhelanise neenkqubo zokusebenza.
    2 Khetha imo yovavanyo oluqhelekileyo lwe-WIZ-A101 ye-immune analyzer ephathekayo
    3 Vula i-aluminium foil bag package ye-reagent kwaye ukhuphe isixhobo sovavanyo.
    4 Faka ngokuthe tye isixhobo sovavanyo kwi-slot ye-immune analyzer.
    5 Kwiphepha lasekhaya le-interface yokusebenza ye-immune analyzer, cofa u-"Standard" ukufaka ujongano lovavanyo.
    6 Cofa "QC Scan" ukuskena ikhowudi ye-QR kwicala langaphakathi lekhithi; igalelo kit ezinxulumene parameters kwisixhobo kwaye ukhethe uhlobo isampuli.
    Qaphela: Inani lebhetshi nganye yekhithi iya kuskenwa ngexesha elinye. Ukuba inombolo yebhetshi iskeniwe, uze utsibe eli nyathelo.
    7 Khangela ukuhambelana "kweGama leMveliso", "Inombolo yeBatch" njl.
    8 Thatha isampulu yediluent kulwazi olungaguqukiyo, yongeza i-10μL serum/plasma/isampulu yegazi elipheleleyo, kwaye uzixube kakuhle;
    9 Yongeza i-80µL echazwe ngasentla isisombululo esixutywe kakuhle kwiqula lesixhobo sovavanyo;
    10 Emva kokudibanisa isampulu epheleleyo, cofa u-“Timing” kwaye ixesha eliseleyo lovavanyo liya kuboniswa ngokuzenzekelayo kujongano.
    11 Umhlalutyi we-Immune uya kugqiba uvavanyo kunye nohlalutyo ngokuzenzekelayo xa ixesha lokuvavanya lifikelelwe.
    12 Emva kokuba uvavanyo lwe-immune analyser lugqityiwe, iziphumo zovavanyo ziya kuboniswa kujongano lovavanyo okanye zinokujongwa “ngeMbali” kwiphepha lasekhaya lojongano lokusebenza.

    Qaphela: isampuli nganye iya kubhobhozwa ngepayipi ecocekileyo elahlwayo ukuphepha ukungcoliseka komnqamlezo.

    CTNI,MYO,CK-MB-01

    Ukongama

    Ikhithi ichanekile kakhulu, iyakhawuleza kwaye inokuhanjiswa kwiqondo lobushushu begumbi.Kulula ukuyisebenzisa.
    Uhlobo lomfanekiso : ISerum/Plasma/Igazi Elipheleleyo

    Ixesha lokuvavanya: 10-15mins

    Ugcino:2-30℃/36-86℉

    Indlela yokusebenza:Fluorescence Immunochromatographic Assay

     

    Uphawu:

    • Uvakalelo oluphezulu

    • iziphumo zokufunda kwimizuzu eli-15

    • Ukusebenza ngokulula

    • Ukuchaneka okuphezulu

     

    CTNI,MYO,CK-MB-04
    微信图片_20230329161634

     

     

    Unokuthanda kwakhona:

    cTnI

    Ikhithi yokuxilonga yeCardiac Troponin I

    MYO

    Diagnostic Kit for Myoglobin

    D-Dimer

    Ikhithi yokuxilonga ye-D-Dimer


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