Colloidal Gold Blood HBsAg&HCV Gwajin Haɗaɗɗen Haɗaɗɗen Sauri

taƙaitaccen bayanin:

Gwajin Haɗaɗɗen Haɗaɗɗen HBsAg&HCV

Hanyar: Colloidal Gold

 

 


  • Lokacin gwaji:Minti 10-15
  • Lokacin Inganci:Wata 24
  • Daidaito:Fiye da 99%
  • Bayani:1/25 gwaji/akwatin
  • Yanayin ajiya:2 ℃-30 ℃
  • Hanyar:Colloidal Gold
  • Cikakken Bayani

    Tags samfurin

    BAYANIN SAURAYI

    Lambar Samfura Gwajin Combo HBsAg&HCV Shiryawa 20 Gwaje-gwaje/kit, 30kits/CTN
    Suna Gwajin Haɗaɗɗen Haɗaɗɗen HBsAg & HCV
    Rarraba kayan aiki Darasi na III
    Siffofin Babban hankali, Mai sauƙin aiki Takaddun shaida CE/ISO13485
    Daidaito > 97% Rayuwar rayuwa Shekaru Biyu
    Hanya Colloidal Gold OEM/ODM sabis Akwai

     

    CTNI,MYO,CK-MB-01

    fifiko

    Kit ɗin yana da inganci, mai sauri kuma ana iya jigilar shi a cikin ɗaki. Yana da sauƙin aiki.
    Nau'in samfur:serum/plas-ma/jini duka

    Lokacin gwaji:15-20mins

    Adana:2-30℃/36-86℉

    Hanyar: Colloidal Gold

     

    Siffa:

    • Babban m

    • karatun sakamako a cikin mintuna 15-20

    • Sauƙi aiki

    • Babban Daidaito

     

    CTNI,MYO,CK-MB-04

    AMFANI DA NUFIN

    Wannan kit ɗin yana aiki ne don gano in vitro qualitative detection of hepatitis B virus da hepatitisC virus a cikin jinin mutum/plasma/dukan samfurin jini, kuma ya dace da ƙarin bincike na cutar hanta B da ciwon hanta na C, kuma bai dace da gwajin jini ba. Ya kamata a yi nazarin sakamakon da aka samu tare da wasu bayanan asibiti. itis wanda aka yi nufin amfani da shi ta kwararrun likitoci kawai.

    Hanyar gwaji

    1 Karanta umarnin don amfani kuma cikin cikakken tsari tare da umarni don amfani da aikin da ake buƙata don guje wa shafar daidaiton sakamakon gwajin.
    2 Kafin gwajin, ana fitar da kit ɗin da samfurin daga yanayin ajiya kuma a daidaita su zuwa zafin daki kuma a yi masa alama.
    3 Yaga marufi na jakar foil na aluminum, fitar da na'urar gwajin da alama, sannan a sanya shi a kwance akan teburin gwaji.
    4 Samfurin da za a gwada (serum/plasma) an ƙara shi zuwa rijiyoyin S1 da S2 tare da ɗigo 2 ko samfurin da za a gwada (jini duka) an ƙara shi zuwa rijiyoyin S1 da s2 tare da digo 3. Bayan an ƙara samfurin, ana ƙara 1 ~ 2 digo na samfurin dilution a cikin rijiyoyin S1 da S2.an fara lokaci.
    5 Ya kamata a fassara sakamakon gwaji a cikin mintuna 15 ~ 20, idan fiye da minti 20 sakamakon fassarar ba shi da inganci.
    6 Ana iya amfani da fassarar gani a fassarar sakamako.

    Lura: kowane samfurin za a yi bututu ta hanyar pipette mai tsaftataccen zubarwa don guje wa gurɓacewar giciye.

    AIYUKA na asibiti

    Sakamakon WIZHBsag  Sakamakon gwaji na Reagent Reagent Madaidaicin ƙimar daidaituwa:

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

    Adadin daidaituwa mara kyau:

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

    Jimlar adadin daidaituwa:

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

    M Korau Jimlar
    Tabbatacce 190 2 192
    Korau 1 266 267
    Jimlar 191 268 459

     

    Sakamakon WIZHCV  Sakamakon gwaji na Reagent Reagent  

    Madaidaicin ƙimar daidaituwa:

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

    Adadin daidaituwa mara kyau:

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

    Jimlar adadin daidaituwa:

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

       

    M Korau Jimlar
    Tabbatacce 56 2 58
    Korau 2 399 401
    Jimlar 58 401 459

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