I-Pepsinogen I Pepsinogen II kunye ne-Gastrin-17 Combo rapid test kit

inkcazo emfutshane:

Ikhithi yokuxilonga yePepsinogen I/Pepsinogen II/Gastrin-17
uvavanyo lwe-fluorescence immunochromatographic


  • Ixesha lovavanyo:imizuzu eli-10-15
  • Ixesha Elisebenzayo:Iinyanga ezingama-24
  • Ukuchaneka:Ngaphezulu kwe-99%
  • Inkcazo:Uvavanyo/ibhokisi eyi-1/25
  • Ubushushu bokugcina:2℃ -30℃
  • Indlela yokusebenza:uvavanyo lwe-fluorescence immunochromatographic
  • Iinkcukacha zeMveliso

    Iithegi zeMveliso

    Ikhithi yokuxilonga yePepsinogen I/Pepsinogen II/Gastrin-17

    Indlela yokusebenza: uvavanyo lwe-fluorescence immunochromatographic

    Ulwazi lwemveliso

    Inombolo yoMzekelo G17/PGI/PGII Ukupakisha Iimvavanyo ezingama-25/ikhithi, iikhithi ezingama-30/i-CTN
    Igama Ikhithi yokuxilonga yePepsinogen I/Pepsinogen II/Gastrin-17 Ukuhlelwa kwezixhobo Iklasi yesiBini
    Iimbonakalo Uvakalelo oluphezulu, Ukusebenza lula Isatifikethi I-CE/ ISO13485
    Ukuchaneka > 99% Beka ubomi kwishelufa Iminyaka emibini
    Indlela yokusebenza uvavanyo lwe-fluorescence immunochromatographic Inkonzo ye-OEM/ODM Iyafumaneka

    UKUSETYENZISWA OKUJOLISWEYO

    Le khithi iyasebenza ekufumaneni ubungakanani be-Pepsinogen I (PGI) kunye ne-Pepsinogen II kwi-in vitro
    (PGII) kunye neGastrin 17 kwiisampuli ze-serum/plasma/zegazi elipheleleyo lomntu, ukuvavanya iseli ye-gastric oxyntic gland
    umsebenzi, isilonda se-mucosa yesisu kunye ne-atrophic gastritis. Le khithi inika kuphela iziphumo zovavanyo lwePepsinogen I
    (PGI), iPepsinogen II (PGII) kunye neGastrin 17. Iziphumo ezifunyenweyo kufuneka zihlalutywe kunye nezinye iindlela zonyango.
    Ulwazi. Kufuneka lusetyenziswe kuphela ziingcali zezempilo.

    Inkqubo yovavanyo

    1 Ngaphambi kokusebenzisa i-reagent, funda ngononophelo iphakheji kwaye uqhelane neenkqubo zokusebenza.
    2 Khetha imo yovavanyo eqhelekileyo ye-WIZ-A101 portable immune analyzer.
    3 Vula iphakheji ye-reagent yebhegi yefoyile ye-aluminiyam uze ukhuphe isixhobo sovavanyo.
    4 Faka isixhobo sovavanyo ngokuthe tye kwindawo yokuhlaziya umzimba.
    5 Kwiphepha lasekhaya le-interface yokusebenza ye-immune analyzer, cofa u-“Standard” ukuze ungene kwi-interface yovavanyo
    6 Cofa u-“QC Scan” ukuze uskene ikhowudi ye-QR ngaphakathi kwekhithi; iiparameter ezinxulumene nekhithi yokufaka kwisixhobo kunye
    khetha uhlobo lwesampulu.
    Qaphela: Inani ngalinye lebhetshi yekhithi kufuneka liskeniwe kube kanye. Ukuba inani lebhetshi liskeniwe, ngoko ke
    tsiba eli nyathelo.
    7 Jonga ukuhambelana kwe "Igama leMveliso", "Inombolo yeBatch" njl. Kwi-interface yovavanyo kunye nolwazi olukwikhithi
    ileyibhile.
    8 Emva kokuba ulwazi luqinisekisiwe, khupha iisampulu ze-diluents, yongeza i-80µL ye-serum/plasma/igazi elipheleleyo.
    isampuli, kwaye udibanise ngokwaneleyo.
    9 Yongeza i-80µL yesisombululo esixutyiweyo esingentla kumngxuma wesampulu yesixhobo sovavanyo.
    10 Emva kokongeza isampuli epheleleyo, cofa u-“Timing” kwaye ixesha eliseleyo lovavanyo liya kuboniswa ngokuzenzekelayo kwi
    ujongano.
    11 I-immune analyzer izakugqiba uvavanyo kunye nohlalutyo ngokuzenzekelayo xa ixesha lovavanyo lifikile.
    12 Ukubalwa kwesiphumo kunye nokuboniswa
    Emva kokuba uvavanyo oluqhutywa yi-immune analyzer lugqityiwe, iziphumo zovavanyo ziya kuboniswa kwi-interface yovavanyo okanye zinokujongwa
    ngokusebenzisa "Imbali" kwiphepha lasekhaya le-interface yokusebenza.
    I-PGI-PGII-G17-1 Ukubaluleka

    Le khithi ichanekile kakhulu, iyakhawuleza kwaye ingathuthwa kubushushu begumbi. Kulula ukuyisebenzisa, i-app yefowuni ephathwayo inokunceda ekutolikeni iziphumo kwaye izigcine ukuze kube lula ukuzilandelela.

    Uhlobo lwesampuli: iisampulu zegazi/iplasma/igazi elipheleleyo

    Ixesha lovavanyo: 10-15mins

    Indawo yokugcina: 2-30℃/36-86℉

    Indlela yokusebenza: Isigaba Esiqinileyo

    Uphawu:

    • Uvakalelo oluphezulu

    • ukufundwa kweziphumo kwimizuzu eli-15

    • Ukusebenza okulula

    • Uvavanyo olu-2 ngexesha elinye

    I-PGI-PGII-G17-4
    QQ图片20230322140021

    Ukusebenza kweKlinikhi

    Ukusebenza kovavanyo lweklinikhi kwemveliso kuvavanywa ngokuqokelela iisampuli zeklinikhi ezingama-200. Sebenzisa ikhithi ethengiswayo ye-enzyme linked immunosorbent assay njenge-reagent yokulawula. Thelekisa iziphumo zovavanyo lwe-PGI. Sebenzisa i-linearity regression ukuphanda ukuthelekiswa kwazo. Ii-coefficients zokuhambelana kweemvavanyo ezimbini yi-y = 0.964X + 10.382 kunye ne-R=0.9763 ngokwahlukeneyo. Thelekisa iziphumo zovavanyo lwe-PGII. Sebenzisa i-linearity regression ukuphanda ukuthelekiswa kwazo. Ii-coefficients zokuhambelana kweemvavanyo ezimbini yi-y = 1.002X + 0.025 kunye ne-R=0.9848 ngokwahlukeneyo. Thelekisa iziphumo zovavanyo lwe-G-17. Sebenzisa i-linearity regression ukuphanda ukuthelekiswa kwazo. Ii-coefficients zokuhambelana kweemvavanyo ezimbini yi-y = 0.983X + 0.079 kunye ne-R=0.9864 ngokwahlukeneyo.

    Ungathanda kwakhona:

    I-CAL

    Ikhithi yokuxilonga yeCalprotectin(uvavanyo lwe-fluorescence immunochromatographic)

    I-HP-AG

    -Ikhithi yokuxilonga ye-Antigen ukuya kwi-Helicobacter Pylori (Uvavanyo lwe-Fluorescence Immunochromatographic)

    I-HP-AB

    Ikhithi yokuxilonga ye-Antibody To Helicobacter Pylori (Uvavanyo lweFluorescence Immunochromatographic Assay


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