Diagnostic Kit yeHeparin Inosunga Mapuroteni

tsananguro pfupi:

Diagnostic Kit yeHeparin Binding Protein (Fluorescence
Immunochromatographic Assay)

 

 


  • 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 yeHeparin Binding Protein (Fluorescence
    Immunochromatographic Assay)

    Nzira: Fluorescence Immunochromatographic Assay

    Ruzivo rwekugadzira

    Model Number HBP Packing 25 Miedzo / kit, 30kits / CTN
    Zita
    Diagnostic Kit yeHeparin Inosunga Mapuroteni
    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 in vitro yekuona yeheparin inosunga mapuroteni (HBP) muropa rakazara remunhu / plasma sampuro, uye inogona kushandiswa yekubatsira chirwere chekuongorora, sekufema uye kutadza kutenderera kweropa, yakanyanya sepsis, weti turakiti hutachiona muvana, bhakitiriya. utachiona hweganda uye acute bacterial meningitis. Iyi kit inongopa heparin inosunga mapuroteni emhedzisiro, uye mibairo inowanikwa ichashandiswa musanganiswa nerumwe ruzivo rwekiriniki rwekuongorora.

    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 80μL 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 ichaputirwa 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
    HBP Rapid bvunzo

     

     

    Unogonawo kuda:

    cTnI

    Diagnostic Kit yeCardiac Troponin I

    MYO

    Diagnostic Kit yeMyoglobin

    D-Dimer

    Diagnostic Kit yeD-Dimer


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