I-antibody ye-IgM Enterovirus 71 EV71 ikhithi yovavanyo olukhawulezayo EV 71 antibody

inkcazelo emfutshane:

Inombolo yoMfanekiso EV71 IgM Ukupakisha Iimvavanyo ze-25 / ikiti, i-20kits / i-CTN
Igama Ikhithi yokuxilonga ye-Human Enterovirus 71 ( colloidal Gold ) Ukuhlelwa kwesixhobo Udidi II
Iimbonakalo Uvakalelo oluphezulu, ukusebenza ngokulula Isatifikethi CE/ ISO13485
Umzekelo ISerum, iPlasma Beka ubomi kwishelufa Iminyaka emibini
Ukuchaneka > 99% Iteknoloji Igolide yeColloidal
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.EV-71-2
    4-(3)
    4-(4)

    UMGAQO KUNYE NENKQUBO YOKUHLOLA FOB

    UMGAQO

    Inwebu yesixhobo sovavanyo igqunywe nge-anti EV71 ye-antibody kwindawo yovavanyo kunye ne-antibody ye-IgG yebhokhwe kwindawo yolawulo. Iphedi elayibhile iqatywe nge-fluorescence ebhalwe i-anti EV71 antibody kunye ne-IgG yomvundla kwangaphambili. Xa uvavanyo lwesampulu eqinisekileyo, i-antigen ye-EV71 kwisampulu idibanisa ne-fluorescence ebhalwe i-anti EV71 antibody, kwaye yenza umxube wokuzivikela komzimba. Ngaphantsi kwesenzo sechromatography, ukuhamba okuntsonkothileyo kwicala lephepha elifunxayo, xa i-complex iphumelele ummandla wovavanyo, idityaniswe ne-anti EV71 yokugquma i-antibody, yenza into entsha.

    Ukuba i-negative, isampuli ayinayo i-enterovirus 71 IgM antibody, ukwenzela ukuba i-immune complex ingenziwa. Akuyi kubakho umgca obomvu kwindawo yokufumanisa (T). Nokuba ikhona i-antibody ye-Enterovirus 71 IgM kumzekelo okanye ayikho, i-antibody eseleyo ye-colloidal yegolide ene-anti-human IgM monoclonal kunye ne-anti-mouse ye-IgG yebhokhwe egqunywe kwindawo yolawulo lomgangatho (C) iyabophelela. Emva koko i-agglutinates iphuhlisa umbala kwindawo yokulawula umgangatho, kwaye umgca obomvu uya kubonakala kwi (C). Umgca obomvu ngumgangatho ovela kwindawo yokulawula umgangatho (C) ukugweba ukuba kukho iisampuli ezaneleyo kunye nokuba inkqubo yechromatography iyinto eqhelekileyo. Ikwasetyenziswa njengomgangatho wolawulo lwangaphakathi kwii-reagents.

    Inkqubo yoVavanyo:

    1.Iisampulu ezivavanyiweyo zingaba ligazi elipheleleyo, kubandakanywa igazi le-venous okanye igazi le-Peripheral. Igazi elipheleleyo alinakugcinwa emva kokuqokelela. Kufuneka ndisetyenziswe ngokukhawuleza emva kokuqokelela.

    I-2.Iisampulu zeSerum ziqokelelwa ngokwe-aseptically ngokweendlela eziqhelekileyo. Iserum engasebenziyo ubushushu ayinakusetyenziswa. Akukhuthazwa ukusebenzisa i-lipemic, i-turbid okanye i-serum engcolileyo. Yinto encinci kwiserum. Kwaye imvula iya kuchaphazela iziphumo zovavanyo, iisampulu ezinjalo kufuneka zifakwe kwi-centrifuged okanye zihluzwe ngaphambi kokusetyenziswa.

    I-3.Iisampulu ezivavanyiweyo zingaba yi-heparin, i-Sodium citrate okanye i-EDTA i-anticoagulant plasma.

    4.Ngokungqinelana neendlela eziqhelekileyo zokuqokelela isampuli. I-Serum okanye isampuli ye-plasma inokugcinwa efrijini kwi-2-8 ℃ iintsuku ezi-3 kunye ne-cryopreservation engaphantsi kwe-15 ° C kwiinyanga ezi-3.

    5.Zonke iisampulu ziphephe imijikelo yokunyibilika komkhenkce.

    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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