C-creactive protein CRP quick test kit

tsananguro pfupi:

Diagnostic Kit yeC-reactive Protein

 

 


  • Nguva yekuedza:10-15 maminitsi
  • Nguva Yakakodzera:24 mwedzi
  • Kururama:Kupfuura 99%
  • Tsanangudzo:1/25 bvunzo/bhokisi
  • Kuchengetedza tembiricha:2 ℃-30 ℃
  • Nzira:Fluorescence Immunochromatographic Assay
  • Product Detail

    Product Tags

    Diagnostic Kit yeCardiac Troponin I ∕Isoenzyme MB yeCreatine Kinase ∕Myoglobin

    Nzira: Fluorescence Immunochromatographic Assay

    Ruzivo rwekugadzira

    Model Number CRP Packing 25 Miedzo / kit, 30kits / CTN
    Zita Diagnostic Kit yeC-creative protein Instrument classification Kirasi I
    Features High senitivity, Easy operation Chitupa CE/ ISO13485
    Kururama > 99% Sherufu hupenyu Makore maviri
    Methodology Fluorescence Immunochromatographic Assay OEM / ODM sevhisi Avaliable

     

    ZVIRI KUSHANDISA

    Iyi kit inoshanda kune vitro quantitative yekuona C-reactive protein (CRP) muvanhu serum / plasma / yese yeropa samples, yekubatsira kuongororwa kweacute uye kusingaperi kuzvimba kana hutachiona. Izvi
    kit inongopa mhedzisiro yebvunzo yeC-reactive protein, uye mhedzisiro yakawanikwa ichaongororwa pamwe chete nedzimwe ruzivo rwekiriniki.

    Test maitiro

    1 Usati washandisa reagent, verenga pasuru yacho nokungwarira uye uzvizivise nemafambisirwo ekushanda.
    2 Sarudza yakajairika test mode yeWIZ-A101 inotakurika immune analyzer
    3 Vhura iyo aluminium foil bag package ye reagent uye tora bvunzo mudziyo.
    4 Yakachinjika isa mudziyo wekuyedza mune slot ye immune analyzer.
    5 Papeji rekutanga rekushandisa interface yeimmune analyzer, tinya "Standard" kuti upinde muyedzo interface.
    6 Dzvanya "QC Scan" kuti utarise kodhi yeQR padivi remukati rekiti; yekuisa kit ine hukama ma paramita mune chiridzwa uye sarudza mhando yemhando.
    Cherechedza: Nhamba yega yega yekiti yekiti ichaongororwa kwenguva imwe chete. Kana iyo batch nhamba yakaongororwa, saka svetuka danho iri.
    7 Tarisa kuenderana kwe "Zita reChigadzirwa", "Batch Number" nezvimwe pane test interface ine ruzivo pane kit label.
    8 Bvisa sample diluent paruzivo rwakafanana, wedzera 10μL serum/plasma/sample yeropa rose, wonyatsoisanganisa;
    9 Wedzera 80µL yakataurwa yakanyatso kusanganiswa mhinduro mutsime rebvunzo mudziyo;
    10 Mushure mekuwedzera sampuli yekuwedzera, tinya "Nguva" uye yasara nguva yekuyedza inozoratidzwa otomatiki pane interface.
    11 Immune analyzer inozopedzisa kuyedza uye kuongorora kana nguva yekuyedza yasvika.
    12 Mushure mekunge bvunzo neimmune analyzer yapedzwa, mhedzisiro yebvunzo inozoratidzwa pane test interface kana inogona kutariswa kuburikidza ne "Nhoroondo" pane peji repamba rekushanda interface.

    Ongorora: imwe neimwe sampu ichapinzwa nepipette yakachena inoraswa kudzivirira kusvibiswa kwemuchinjiko.

    CTNI,MYO,CK-MB-01

    Superiority

    Iyo kit ndeyepamusoro, inokurumidza uye inogona kutakurwa pakamuri tembiricha.Iri nyore kushanda.
    Muenzaniso wemhando: Serum / Plasma / Ropa Rose

    Nguva yekuedza: 10-15mins

    Kuchengetedza:2-30℃/36-86℉

    Nzira: Fluorescence Immunochromatographic Assay

     

    Feature:

    • High sensitive

    • mhedzisiro kuverenga mumaminitsi gumi nemashanu

    • Easy operation

    • Kururama kwepamusoro

     

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

     

     

    Unogonawo kuda:

    cTnI

    Diagnostic Kit yeCardiac Troponin I

    MYO

    Diagnostic Kit yeMyoglobin

    D-Dimer

    Diagnostic Kit yeD-Dimer


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