Ikhithi yokuxilonga yeProgesterone (i-fluorescence immunochromatographic assay)

inkcazelo emfutshane:


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

    Iithegi zeMveliso

    I-Diagnostic Kit yeProgesterone(uvavanyo lwe-fluorescence immunochromatographic)
    Ukusetyenziswa kwe-in vitro diagnostic kuphela

    Nceda ufunde le phakheji ifake ngononophelo phambi kokuba uyisebenzise kwaye ulandele ngokungqongqo imiyalelo.Ukuthembeka kweziphumo zovavanyo akunakuqinisekiswa ukuba kukho nakuphi na ukutenxa kwimiyalelo kolu fakelo lwephakheji.

    UKUSETYENZISWA OKUHLOSIWEYO
    I-Diagnostic Kit yeProgesterone (i-fluorescence immunochromatographic assay) luvavanyo lwe-fluorescence immunochromatographic yokufumanisa ubungakanani beProgesterone (PROG) kwi-serum yabantu okanye kwiplasma, isetyenziselwa ukuxilongwa kwe-progesterone ngokungaqhelekanga izifo ezinxulumene nazo.Zonke iisampuli ezilungileyo kufuneka ziqinisekiswe ngezinye iindlela. .Olu vavanyo lwenzelwe ukusetyenziswa kweengcali zezempilo kuphela.

    USHWANKATHELO
    Iprogesterone yi-hormone ebalulekileyo edlala indima ebalulekileyo ekulawuleni umjikelezo wokuya esikhathini kwaye ibalulekile ekugcineni ukukhulelwa.Ukuxinwa kweprogesterone kwi-serum kwanda ngokukhawuleza emva kwe-ovulation.Ingumqondiso othembekileyo we-ovulation yendalo okanye ukufakwa kwe-ovulation.

    UMGAQO WENKQUBO
    I-membrane yesixhobo sokuvavanya ifakwe kwi-conjugate ye-BSA kunye ne-PROG kummandla wokuvavanya kunye nebhokhwe yokulwa nomvundla we-IgG kwingingqi yokulawula.Iphedi yesiphawuli iqatywe nge-fluorescence uphawu lwe-anti-PROG antibody kunye nomvundla we-IgG kwangaphambili.Xa uvavanyo lwesampulu, i-PROG kwisampulu idibanisa kunye ne-fluorescence ephawulwe kwi-anti-PROG antibody, kwaye yenze umxube wokuzivikela komzimba.Ngaphantsi kwesenzo se-immunochromatography, ukuhamba okuyinkimbinkimbi kwicala lephepha lokufunxa, xa i-complex iphumelele ummandla wovavanyo, I-marker ye-fluorescent yamahhala iya kudibaniswa ne-PROG kwi-membrane. Uxinzelelo lwe-PROG kwisampulu lunokubonwa ngovavanyo lwe-fluorescence immunoassay.

    IIREGENTS KUNYE NEZINTO EZIBONISWAYO
    Amacandelo ephakheji ye-25T:

    Ikhadi lokuvavanya ifoyile nganye efakwe kwi-desiccant 25T
    Isampulu yediluyinti 25T
    Faka ipakethi 1

    IZINTO EZIFUNEKAYO KODWA AKUNIKEZWA
    Isampulu yokuqokelela isitya,ixesha

    UKUQOKELELWA KWEsampuli NOKUGCINWA
    1.Iisampulu ezivavanyiweyo zingaba serum, i-heparin anticoagulant plasma okanye i-EDTA anticoagulant plasma.

    2.Ngokungqinelana neendlela eziqhelekileyo zokuqokelela isampuli.I-Serum okanye isampuli ye-plasma inokugcinwa efrijini kwi-2-8 ℃ ye-7days kunye ne-cryopreservation engaphantsi kwe-15 ° C kwiinyanga ezi-6.
    3.Zonke iisampulu ziphephe imijikelo yokunyibilika komkhenkce.

    INKQUBO YOVAVANYO
    Nceda ufunde incwadi yokusebenza kwesixhobo kunye nokufakwa kwephakheji phambi kovavanyo.

    I-1.Lay eceleni zonke ii-reagents kunye neesampuli kwiqondo lokushisa.
    2Vula i-Portable Immune Analyzer (WIZ-A101), ngenisa igama lokungena kwiakhawunti ngokwendlela yokusebenza yesixhobo, kwaye ngenisa ujongano lokubona.
    3.Skena ikhowudi yokuchaza ukuze uqinisekise into yovavanyo.
    4.Khupha ikhadi lovavanyo kwibhegi yefoyile.
    5.Faka ikhadi lovavanyo kwi-slot yekhadi, scan ikhowudi ye-QR, kwaye unqume into yovavanyo.
    6.Yongeza i-20μL ye-serum okanye isampuli yeplasma kwisampulu ye-diluent, kwaye udibanise kakuhle.
    7.Yongeza i-80μL yesisombululo sesampulu kwisampulu kakuhle yekhadi.
    8.Klikha iqhosha elithi "standard test", emva kwemizuzu eyi-10, isixhobo siya kubona ngokuzenzekelayo ikhadi lovavanyo, sinokufunda iziphumo kwisikrini sokubonisa isixhobo, kwaye sirekhode / siprinte iziphumo zovavanyo.
    9.Jonga kumyalelo we-Portable Immune Analyzer(WIZ-A101).

    IZIPHUMO ZOMVAVANYO KUNYE UTOLIKO

    Iqonga

    Uluhlu(ng/mL)

    Indoda

    0.1-0.9

    Ibhinqa

    isigaba se-follicular / ixesha le-ovulatory

    0.3-1.5

    Isigaba seLuteal

    5.2-18.5

    Ukuyeka ukuya exesheni

    <0.8

    .Le datha ingentla isiphumo sovavanyo lwe-PROG ye-reagent, kwaye kucetyiswa ukuba ilabhoratri nganye kufuneka iseke uluhlu lwe-PROG yokubona ixabiso elifanelekileyo kuluntu kulo mmandla.Ezi ziphumo zingentla zezereferensi kuphela.
    .Iziphumo zale ndlela zisebenza kuphela kuluhlu lwereferensi olusekwe kule ndlela, kwaye akukho kuthelekiswa ngokuthe ngqo kunye nezinye iindlela.
    .Ezinye izinto zinokubangela iimpazamo kwiziphumo zokubona, kubandakanywa nezizathu zobugcisa, iimpazamo zokusebenza kunye nezinye izinto zesampulu.

    UKUGCINWA NOZINZI
    1.Ikhithi ziinyanga ezili-18 zobomi beshelufa ukusukela kumhla wokwenziwa.Gcina iikhithi ezingasetyenziswanga kwi-2-30°C.MUSA UKUMKHENZA.Musa ukusebenzisa ngaphaya komhla wokuphelelwa.

    2.Musa ukuvula isingxobo esitywiniweyo de ube ulungele ukwenza uvavanyo, kwaye uvavanyo lokusetyenziswa olunye lucetyiswa ukuba lusetyenziswe phantsi kwendawo efunekayo (iqondo lobushushu 2-35℃, ukufuma 40-90%) ngaphakathi kwemizuzu engama-60 ngokukhawuleza. kangangoko kunokwenzeka.
    3Isampuli yokuxutywa isetyenziswa ngoko nangoko emva kokuvulwa.

    IZILUMKISO NEMIGAQO
    .Ikhithi kufuneka itywinwe kwaye ikhuselwe kumswakama.

    .Yonke imizekelo emihle iya kuqinisekiswa ngezinye iindlela.
    .Yonke imizekelo iya kuphathwa njengongcoliseko olunokubakho.
    .USUKU sebenzisa i-reagent ephelelwe lixesha.
    . MUSA ukutshintshanisa iirejenti phakathi kweekhithi ezineqashiso ezahlukeneyo No..
    .USUKU phinda usebenzise amakhadi ovavanyo kunye naziphi na izincedisi ezilahlwayo.
    .I-Misoperation, isampuli eninzi okanye encinci inokukhokelela ekuphambukeni kweziphumo.

    LUKUXELELA
    .Njengalo naluphi na uvavanyo olusebenzisa izilwa-buhlungu zegundane, kunokwenzeka ukuba kukho ukuphazanyiswa ngama-anti-mouse antibodies (HAMA) kwi-specimen.Iisampulu ezisuka kwizigulane ezifumene amalungiselelo ee-antibodies ze-monoclonal zokuxilongwa okanye unyango zingaquka i-HAMA.Imizekelo enjalo inokubangela ubuxoki okanye iziphumo ezingalunganga.

    .Esi siphumo sovavanyo kuphela kwireferensi yeklinikhi, akufanele isebenze njengesiseko kuphela sokuxilongwa kweklinikhi kunye nonyango, izigulane zolawulo lwezonyango kufuneka ziqwalaselwe ngokubanzi kunye neempawu zayo, imbali yezonyango, ezinye iimviwo zebhubhoratri, impendulo yonyango, i-epidemiology kunye nolunye ulwazi. .
    .Le reagent isetyenziselwa kuphela iimvavanyo ze-serum kunye ne-plasma.Isenokungafumani ziphumo zichanekileyo xa isetyenziselwa ezinye iisampulu ezinje ngamathe nomchamo, njl.

    IIMPAWU ZOKUSEBENZA

    Umgca 0.5ng/mL ukuya ku-50ng/mL ukutenxa okuhambelanayo: -15% ukuya +15%.
    Umgca wolungelelwaniso i-coefficient:(r)≥0.9900
    Ukuchaneka Izinga lokubuyisela liya kuba phakathi kwe-85% - 115%.
    Ukuphindaphinda CV≤15%
    Ukuchaza ngokuthe ngqo(Akukho nanye kwizinto ezivavanyiweyo eziye zaphazamisa kuvavanyo)

    Ungenelelo

    Ukugxininiswa kokuphazamiseka

    E2

    500ng/mL

    T

    500ng/mL

    Kor

    500ng/mL

    E3

    100ng/mL

    17β-E2

    100ng/mL

    RIMIZEKELO
    1.Hansen JH, et al.HAMA Ukuphazamiseka kunye ne-Murine Monoclonal Antibody-Based Immunoassays [J] .J ye-Clin Immunoassay, 1993, 16: 294-299.

    2.Levinson SS.Ubume be-Heterophilic Antibodies kunye nendima kwi-Immunoassay Interference[J].J ye-Clin Immunoassay,1992,15:108-114.

    Isitshixo kwiisimboli ezisetyenzisiweyo:

     t11-1 In Vitro Diagnostic Medical Isixhobo
     tt-2 Umenzi
     tt-71 Gcina kwi-2-30 ℃
     tt-3 Umhla WOKUPHELELWA
     tt-4 Musa Ukuphinda Usebenzise
     tt-5 ISILUMKO
     tt-6 Qhagamshelana neMiyalelo yokuSetyenziswa

    Xiamen Wiz Biotech CO.,LTD
    Idilesi: 3-4 Floor,NO.16 Building,Bio-medical Workshop,2030 Wengjiao West Road,Haicang District,361026,Xiamen,China
    Umnxeba: + 86-592-6808278
    Ifeksi: + 86-592-6808279


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