Kit ɗin Gano don Hormone mai Ƙarfafa thyroid (ƙimar fluorescence immunochromatographic)

taƙaitaccen bayanin:


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

    Tags samfurin

    Kit ɗin bincike donHormone mai motsa thyroidImmunochromatographic assay)
    Don bincikar in vitro amfani kawai
    Da fatan za a karanta wannan fakitin a hankali kafin amfani kuma a bi umarnin sosai.Ba za a iya tabbatar da amincin sakamakon kima ba idan akwai wasu sabani daga umarnin a cikin wannan fakitin.

    AMFANI DA NUFIN
    Kit ɗin Diagnostic for Thyroid Stimulating Hormone (fluorescence immunochromatographic assay) ne mai fluorescence immunochromatographic kididdigar don ƙididdige yawan gano Thyroid Stimulating Hormone (TSH) a cikin jini ko plasma, wanda aka fi amfani dashi a cikin kimanta aikin pituitary-thyroid.Duk samfuran tabbatacce dole ne a tabbatar da su ta wasu hanyoyin.Anyi nufin wannan gwajin don amfanin ƙwararrun kiwon lafiya kawai.

    TAKAITACCEN
    Babban ayyuka na TSH: 1, inganta saki na thyroid hormones, 2, inganta kira na T4, T3, ciki har da ƙarfafa aikin famfo iodine, inganta aikin peroxidase, inganta kira na globulin thyroid da tyrosine iodide.

    KA'IDAR HANYA
    An lulluɓe jikin na'urar gwajin tare da antibody TSH akan yankin gwajin da goat anti-zomo IgG antibody akan yankin sarrafawa.Label pad an lullube shi ta hanyar walƙiya mai lakabin antibody TSH da zomo IgG a gaba.Lokacin gwada ingantaccen samfurin, antigen na TSH a cikin samfurin yana haɗuwa tare da kyalli mai lakabin antibody TSH, kuma ya samar da cakuda rigakafi.A karkashin aikin da immunochromatography, da hadaddun ya kwarara a cikin shugabanci na absorbent takarda, a lokacin da hadaddun ya wuce gwajin yankin, shi a hade tare da anti-TSH shafi antibody, Forms sabon complex.TSH matakin ne tabbatacce dangantaka da kyalli siginar, da kuma taro na TSH. a cikin samfurin za a iya gano ta hanyar fluorescence immunoassay assay.

    REAgents DA KAYAN DA AKA BAYAR

    Abubuwan kunshin 25T
    .Katin gwajin daidaiku da foil ɗin da aka shayar da shi tare da 25T na busa
    .Sample diluents
    . Kunshin saka

    KAYAN DA AKE BUKATA AMMA BA'A SAMU BA
    Samfurin tarin akwati, mai ƙidayar lokaci

    MISALI TATTAUNAWA DA AJIYA
    1. Samfuran da aka gwada na iya zama jini, heparin anticoagulant plasma ko EDTA anticoagulant plasma.

    2.According ga daidaitattun dabarun tattara samfurin.Za'a iya adana ruwan magani ko samfurin plasma a cikin firiji a 2-8 ℃ na tsawon kwanaki 7 kuma ana kiyaye cryopreservation ƙasa -15 ° C na watanni 6.
    3.All samfurin guje wa daskare-narke hawan keke.

    HANYAR ASSAY
    Hanyar gwaji na kayan aiki duba jagorar immunoanalyzer.Hanyar gwajin reagent shine kamar haka

    1.Lay a gefe duk reagents da samfurori zuwa dakin zafin jiki.
    2.Bude Portable Immune Analyzer (WIZ-A101), shigar da kalmar sirri shiga asusu bisa ga tsarin aiki na kayan aiki, da kuma shigar da ganowa dubawa.
    3.Scan da lambar haƙori don tabbatar da gwajin abu.
    4.Dauki katin gwaji daga jakar foil.
    5.Saka katin gwaji a cikin ramin katin, duba lambar QR, kuma ƙayyade abin gwajin.
    6.Add 20μL serum ko plasma samfurin zuwa samfurin diluent, da kuma Mix da kyau ..
    7.Add 80μL samfurin bayani don samfurin rijiyar katin.
    8. Danna maɓallin "gwajin misali", bayan minti 15, kayan aiki za su gano katin gwajin ta atomatik, zai iya karanta sakamakon daga allon nuni na kayan aiki, kuma rikodin / buga sakamakon gwajin.
    9. Koma zuwa ga umarnin Portable Immune Analyzer (WIZ-A101).

    SAKAMAKON JARRABAWA DA FASSARA
    .Bayanan da ke sama sakamakon gwajin reagent na TSH ne, kuma ana ba da shawarar cewa kowane dakin gwaje-gwaje ya kafa kewayon ƙimar gano TSH wanda ya dace da yawan jama'a a wannan yanki.Sakamakon da ke sama don tunani ne kawai.
    .Sakamakon wannan hanyar yana aiki ne kawai ga jeri na tunani da aka kafa a cikin wannan hanyar, kuma babu kwatankwacin kai tsaye da sauran hanyoyin.
    .Wasu dalilai kuma na iya haifar da kurakurai a cikin sakamakon ganowa, gami da dalilai na fasaha, kurakuran aiki da sauran abubuwan samfuri.

    AJIYA DA KWANTA
    1.The kit ne 18 watanni shiryayye-rai daga ranar da aka yi.Ajiye kayan da ba a yi amfani da su ba a 2-30 ° C.KAR KA DANKE.Kar a yi amfani da bayan ranar karewa.

    2.Kada ku buɗe jakar da aka rufe har sai kun shirya don yin gwaji, kuma ana ba da shawarar yin amfani da gwajin amfani ɗaya a ƙarƙashin yanayin da ake buƙata (zazzabi 2-35 ℃, zafi 40-90%) a cikin 60 mins da sauri. kamar yadda zai yiwu.
    3.Sample diluent ana amfani da shi nan da nan bayan an bude shi.

    GARGADI DA TSIRA
    .Kit ɗin yakamata a rufe shi kuma a kiyaye shi daga danshi.

    .Duk samfurori masu inganci za a inganta su ta wasu hanyoyin.
    .Duk samfuran za a kula da su azaman masu gurɓata yanayi.
    .KADA KA yi amfani da reagent da ya ƙare.
    .KADA KA musanya reagents tsakanin kits tare da kuri'a daban-daban No..
    .KADA KA sake amfani da katunan gwaji da duk wani kayan haɗi da za'a iya zubarwa.
    .Misoperation, wuce kima ko kadan samfurin iya haifar da sabawa sakamakon.

    LIMITATION
    Kamar yadda yake tare da kowane gwajin amfani da ƙwayoyin rigakafi na linzamin kwamfuta, akwai yuwuwar kutsawa daga ƙwayoyin rigakafin linzamin kwamfuta na ɗan adam (HAMA) a cikin samfurin.Samfura daga marasa lafiya waɗanda suka karɓi shirye-shiryen rigakafin ƙwayoyin cuta na monoclonal don ganewar asali ko jiyya na iya ƙunsar HAMA.Irin waɗannan samfurori na iya haifar da sakamako mara kyau na ƙarya ko ƙarya.

    .Wannan sakamakon gwajin shine kawai don tunani na asibiti, bai kamata ya zama tushen kawai don ganewar asibiti da magani ba, kula da lafiyar marasa lafiya ya kamata a yi la'akari da shi sosai tare da bayyanar cututtuka, tarihin likita, sauran gwaje-gwaje na dakin gwaje-gwaje, amsawar magani, cututtukan cututtuka da sauran bayanai. .
    .Wannan reagent ana amfani dashi kawai don gwajin jini da jini.Maiyuwa baya samun ingantaccen sakamako idan aka yi amfani da shi don wasu samfura kamar yau da fitsari da sauransu.

    HALAYEN YI

    Linearity 0.5μIU/ml zuwa 100μIU/ml bambancin dangi: -15% zuwa +15%.
        Matsakaicin daidaitawar layi:(r)≥0.9900
    Daidaito Adadin dawowa zai kasance cikin 85% - 115%.
    Maimaituwa CV≤15%
    Musamman(Babu ɗaya daga cikin abubuwan da aka gwada wanda aka gwada wanda ya tsoma baki a cikin binciken)   

    Tsangwama

    Matsalolin tsaka-tsaki

    HCG

    2000mIU/ml

    FSH

    500mIU/ml

    LH

    500mIU/ml

    NASARA
    1.Hansen JH, et al.HAMA Tsangwama tare da Murine Monoclonal Antibody-Based Immunoassays[J].J na Clin Immunoassay,1993,16:294-299.
    2.Levinson SS.Yanayin Heterophilic Antibodies da Matsayin Tsangwama na Immunoassay[J].J na Clin Immunoassay,1992,15:108-114.

    Maɓalli ga alamomin da aka yi amfani da su:

     t11-1 In Vitro Diagnostic Medical Na'urar
     tt-2 Mai ƙira
     tt-71 Adana a 2-30 ℃
     tt-3 Ranar Karewa
     tt-4 Kada a sake amfani
     tt-5 HANKALI
     tt-6 Tuntuɓi Umarnin Don Amfani

    Kudin hannun jari Xiamen Wiz Biotech Co.,Ltd
    Adireshi: 3-4 Floor, NO.16 Gina, Bio-Likita Bitar, 2030 Wengjiao West Road, Haicang District, 361026, Xiamen, China
    Lambar waya: + 86-592-6808278
    Fax: + 86-592-6808279


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