Kit ɗin gwajin Jini na IgE FIA

taƙaitaccen bayanin:

Kit ɗin bincike don Jimlar IgE

Hanyar: Fluorescence Immunochromatographic Assay

 


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

    Tags samfurin

    Bayanan samarwa

    Lambar Samfura Jimlar IgE Shiryawa 25 Gwaje-gwaje/kit, 30kits/CTN
    Suna Kit ɗin bincike don Jimlar IgE Rarraba kayan aiki Darasi na II
    Siffofin Babban hankali, Mai sauƙin aiki Takaddun shaida CE/ISO13485
    Daidaito > 99% Rayuwar rayuwa Shekaru Biyu
    Hanya Fluorescence Immunochromatographic Assay
    OEM/ODM sabis Akwai

     

    FT4-1

    Takaitawa

    Immunoglobulin E (IgE) ita ce mafi ƙarancin ƙwayar cuta a cikin jini. Gabaɗaya, ƴan shekara 5 zuwa 7 suna samun izinin barin manya .Tsakanin shekaru 10 zuwa 14, matakan IgE na iya zama sama da na manya. Bayan shekaru 70, matakan IgE na iya raguwa kaɗan kuma su kasance ƙasa da matakan da aka gani a cikin manya waɗanda ke ƙasa da shekaru 40.
    Koyaya, matakin al'ada na IgE ba zai iya ware cututtukan rashin lafiyan ba. Sabili da haka, a cikin bambance-bambancen ganewar cututtuka na rashin lafiyan jiki da marasa lafiya, ƙididdigar ƙididdiga na matakin IgE na mutum yana da mahimmanci kawai idan aka yi amfani da shi tare da wasu gwaje-gwaje na asibiti.

     

    Siffa:

    • Babban m

    • karatun sakamako a cikin mintuna 15

    • Sauƙi aiki

    • Farashin kai tsaye na masana'anta

    • buƙatar inji don karatun sakamako

    FT4-3

    Amfani da Niyya

    Wannan kit ɗin yana aiki ne don gano ƙididdigar ƙididdigewa na jimlar Immunoglobulin E (T-IgE) a cikin maganin ɗan adam/plasma/samfurori na jini duka kuma ana amfani da shi don cututtukan Allergic. Kit ɗin yana ba da sakamakon gwajin jimlar Immunoglobulin E (T-IgE) kawai. Za a bincika sakamakon da aka samu tare da sauran bayanan asibiti. Dole ne kawai ƙwararrun kiwon lafiya su yi amfani da shis.

    Hanyar gwaji

    1 Amfani da šaukuwa na rigakafi analyzer
    2 Bude fakitin jakar foil na aluminium na reagent kuma fitar da na'urar gwaji.
    3 Saka na'urar gwaji a tsaye a cikin ramin mai nazarin rigakafi.
    4 A shafi na gida na aikin dubawar rigakafi, danna "Standard" don shigar da dubawar gwaji.
    5 Danna "QC Scan" don duba lambar QR a gefen ciki na kit; Abubuwan shigar da abubuwan da ke da alaƙa cikin kayan aiki kuma zaɓi nau'in samfuri. Lura: Kowane adadin adadin kayan aikin za a duba shi na lokaci ɗaya. Idan an duba lambar batch, to
    tsallake wannan matakin.
    6 Bincika daidaiton "Sunan samfur", "Lambar Batch" da dai sauransu akan gwajin gwaji tare da bayani akan alamar kit.
    7 Fara ƙara samfurin idan akwai tabbataccen bayani:Mataki 1:a fitar da samfurin diluents, ƙara 80µL na serum/plasma/dukan samfurin jini, sannan a gauraya sosai.

    Mataki 2: Ƙara 80µL na sama gauraye bayani a cikin samfurin rami na gwajin na'urar.

    Mataki na 3:Bayan cikakken samfurin ƙari, danna "Lokaci" kuma sauran lokacin gwajin za a nuna ta atomatik akan ƙirar

    8 Bayan cikakken ƙarin samfurin, danna "Lokaci" kuma sauran lokacin gwajin za a nuna ta atomatik akan mu'amala.
    9 Mai nazarin rigakafi zai kammala gwaji ta atomatik da bincike lokacin da lokacin gwaji ya kai.
    10 Bayan an gama gwajin rigakafin rigakafi, za a nuna sakamakon gwajin akan gwajin gwaji ko kuma ana iya duba shi ta hanyar “Tarihi” akan shafin gida na mu’amala.

    Masana'anta

    nuni

    nuni1

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