Colloidal Gold Blood HBsAg & HCV Rapid Combo Rapid Test

inkcazelo emfutshane:

Uvavanyo lwe-HBsAg & HCV olukhawulezayo lweCombo

Indlela yokusebenza:Igolide yeColloidal

 

 


  • Ixesha lovavanyo:10-15 imizuzu
  • Ixesha elisebenzayo:Iinyanga ezingama-24
  • Ukuchaneka:Ngaphezulu kwe-99%
  • Inkcazo:1/25 uvavanyo / ibhokisi
  • Ubushushu bokugcina :2℃-30℃
  • Indlela yokusebenza:Igolide yeColloidal
  • Iinkcukacha zeMveliso

    Iithegi zeMveliso

    INGCACISO YEMVELISO

    Inombolo yoMzekelo HBsAg & HCV Combo uvavanyo Ukupakisha Iimvavanyo ezingama-20 / ikhithi, 30kits/CTN
    Igama Uvavanyo lwe-HBsAg kunye ne-HCV ekhawulezayo yeCombo
    Ukuhlelwa kwesixhobo Udidi III
    Iimbonakalo Uvakalelo oluphezulu, ukusebenza ngokulula Isatifikethi CE/ ISO13485
    Ukuchaneka > 97% Beka ubomi kwishelufa Iminyaka emibini
    Indlela yokusebenza Igolide yeColloidal Inkonzo ye-OEM/ODM Iyafumaneka

     

    CTNI,MYO,CK-MB-01

    Ukongama

    Ikhithi ichanekile kakhulu, iyakhawuleza kwaye inokuhanjiswa kwiqondo lobushushu begumbi.Kulula ukuyisebenzisa.
    Uhlobo lomzekelo :i-serum/i-plasm-ma/igazi elipheleleyo

    Ixesha lokuvavanya: 15-20mins

    Ugcino:2-30℃/36-86℉

    Indlela yokusebenza:Igolide yeColloidal

     

    Uphawu:

    • Uvakalelo oluphezulu

    • iziphumo zokufunda kwimizuzu eyi-15-20

    • Ukusebenza ngokulula

    • Ukuchaneka okuphezulu

     

    CTNI,MYO,CK-MB-04

    UKUSETYENZISWA OKUHLOSIWEYO

    Le khithi isetyenziswa ekubhaqweni okusemgangathweni kwe-in vitro yentsholongwane ye-hepatitis B kunye nentsholongwane ye-hepatitisC kwiserum yabantu / iplasma / isampulu yegazi lonke, kwaye ikulungele ukuxilongwa kwentsholongwane ye-hepatitis B kunye nosulelo lwentsholongwane ye-hepatitis C, kwaye ayifanelekanga ukuhlolwa kwegazi. Iziphumo ezifunyenweyo kufuneka zihlalutywe ngokubambisana nolunye ulwazi lweklinikhi. isifo senzelwe ukusetyenziswa ngabasebenzi bezonyango kuphela.

    Inkqubo yovavanyo

    1 Funda imiyalelo yokusetyenziswa kunye nokuhambelana ngokungqongqo kunye nomyalelo wosetyenziso olufunekayo ukuze ugweme ukuchaphazela ukuchaneka kweziphumo zovavanyo.
    2 Ngaphambi kovavanyo, ikhithi kunye nesampulu zikhutshwa kwimeko yogcino kwaye zilinganiswe kwiqondo lobushushu begumbi kwaye zimakishwe.
    3 Ukukrazula ipakethe yefoyile ye-aluminiyam, khupha isixhobo sovavanyo kwaye usiphawule, emva koko usibeke ngokuthe tye kwitafile yovavanyo.
    4 Isampuli yokuvavanya (i-serum / i-plasma) yongezwa kwi-S1 kunye ne-S2 imithombo kunye ne-2 yehla okanye isampuli yokuvavanya (igazi elipheleleyo) yongezwa kwi-S1 kunye ne-s2 kunye namathontsi e-3. Emva kokuba isampulu yongezwe, i-1 ~ 2 ithontsi yesampulu yokuxutywa yongezwa kwiqula le-S1 kunye ne-S2 kunyeixesha liqalisiwe.
    5 Iziphumo zovavanyo kufuneka zitolikwe kwimizuzu eli-15 ukuya kwengama-20, ukuba ngaphezulu kwemizuzu engama-20 iziphumo ezitolisiweyo azikho mthethweni.
    6 Ukutolika okubonwayo kungasetyenziswa kwisiphumo sokutolika.

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

    INTSEBENZO YOKHILINI

    Iziphumo zeWIZ zeHBsag  Iziphumo zovavanyo lweReference reagent Izinga elincomekayo lokuzenzekela :

    99.48%(95%C.1.97.09%~99.91%)

    Ireyithi yeziganeko ezimbi :

    99.25%(95%C.1.97.32%~99.80%)

    Umlinganiselo opheleleyo weziganeko :

    99.35%(95%C1.9810%~99.78%)

    Okuhle Ibi Iyonke
    Positive 190 2 192
    Ibi 1 266 267
    Iyonke 191 268 459

     

    Iziphumo zeWIZ zeHCV  Iziphumo zovavanyo lweReference reagent  

    Izinga elincomekayo lokuzenzekela :

    96.55%(95%C1.88.27%~99.05%)

    Ireyithi yeziganeko ezimbi :

    99.50%(95%C.1.98.20%~99.86%)

    Umlinganiselo opheleleyo weziganeko :

    99.13%(95%C.1.97.78%~99.66%)

       

    Okuhle Ibi Iyonke
    Positive 56 2 58
    Ibi 2 399 401
    Iyonke 58 401 459

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