Ikhithi yokuxilonga yeTotal Triiodothyronine(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 ye-Total Triiodothyronine (i-fluorescence immunochromatographic assay) luvavanyo lwe-fluorescence immunochromatographic yokufumanisa ubuninzi be-Total Triiodothyronine (TT3) kwi-serum yomntu okanye i-plasma, esetyenziselwa ukuvavanya umsebenzi we-thyroid. kufuneka ziqinisekiswe ngezinye iindlela.Olu vavanyo lwenzelwe ukusetyenziswa kweengcali zezempilo kuphela.

USHWANKATHELO
I-Triiodothyronine (T3) ubunzima bemolekyuli 651D.Yeyona ndlela iphambili esebenzayo yehomoni ye-thyroid.Iyonke i-T3(Itotali ye-T3, i-TT3) kwi-serum yahlulwe yaba ziindidi ezibophelelayo nezisimahla.I-99.5 % ye-TT3 ibophelela kwi-serum i-Thyroxine Binding Proteins(TBP), kunye ne-T3 yasimahla (i-T3 yasimahla) ibalelwa kwi-0.2 ukuya kwi-0.4%.I-T4 kunye ne-T3 zithatha inxaxheba ekugcineni nasekulawuleni umsebenzi we-metabolic womzimba.Imilinganiselo ye-TT3 isetyenziselwa ukuvavanya imeko yokusebenza kwe-thyroid kunye nokuxilongwa kwezifo.I-TT3 yonyango luphawu oluthembekileyo lokuxilongwa kunye nokusebenza kakuhle kwe-hyperthyroidism kunye ne-hypothyroidism.Ukumiselwa kwe-T3 kubaluleke kakhulu ekuxilongweni kwe-hyperthyroidism kune-T4.

UMGAQO WENKQUBO

I-membrane yesixhobo sokuvavanya ifakwe kwi-conjugate ye-BSA kunye ne-T3 kwindawo yokuvavanya kunye nebhokhwe yokulwa nomvundla we-IgG kwingingqi yokulawula.Iphedi yokumakisha iqatywe nge-fluorescence uphawu lwe-anti-T3 antibody kunye nomvundla we-IgG kwangaphambili.Xa uvavanyo lwesampulu, i-TT3 kwisampulu idibanisa kunye ne-fluorescence ephawulwe kwi-anti-T3 antibody, kwaye yenze umxube wokuzivikela komzimba.Ngaphantsi kwesenzo se-immunochromatography, ukuhamba okuyinkimbinkimbi kwicala lephepha elifunxayo, xa i-complex iphumelele ummandla wovavanyo, I-marker ye-fluorescent yamahhala iya kudibaniswa ne-T3 kwi-membrane.I-concentration ye-TT3 i-negative correlation for signal fluorescence, kunye Uxinzelelo lwe-TT3 kwisampulu lunokubonwa ngovavanyo lwe-fluorescence immunoassay.

IIREGENTS KUNYE NEZINTO EZIBONISWAYO

Amacandelo ephakheji ye-25T:
.Ikhadi lovavanyo lwefoyile nganye efakwe kwi-desiccant 25T
.Isisombululo 25T
.B isisombululo 1
.Fakela ipakethe 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
Inkqubo yovavanyo yesixhobo bona incwadana ye-immunoanalyzer.Inkqubo yovavanyo lwe-reagent ngolu hlobo lulandelayo
I-1.Lay eceleni zonke ii-reagents kunye neesampuli kwiqondo lokushisa.
2.Vula i-Portable Immune Analyzer (WIZ-A101), faka igama lokungena kwi-akhawunti ngokwendlela yokusebenza yesixhobo, kwaye ungenise 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-30μL serum okanye isampuli yeplasma kwisisombululo, kwaye udibanise kakuhle.
7.Yongeza isisombululo se-20μL B kumxube ongentla, kwaye udibanise kakuhle.
8.Shiya umxube imizuzu engama-20.
9.Yongeza i-80μL umxube kwisampulu yequla lekhadi.
10.Cofa iqhosha elithi “standard test”, emva kwemizuzu eyi-10, isixhobo siya kubona ngokuzenzekelayo ikhadi lovavanyo, siyakwazi ukufunda iziphumo kwiscreen sokubonisa sesixhobo, kwaye sirekhode/siprinte iziphumo zovavanyo.
11.Jonga kumyalelo we-Portable Immune Analyzer (WIZ-A101).

IINDLELA EZILINDELEKILEYO

TT3 uluhlu oluqhelekileyo: 0.5-2.5ng / mL
Kucetyiswa ukuba ilabhoratri nganye iseke uluhlu lwayo oluqhelekileyo olumele izigulane zayo.

IZIPHUMO ZOMVAVANYO KUNYE UTOLIKO
.Le datha ingentla lithuba lereferensi elisekwe kwidatha yobhaqo yale khithi, kwaye kucetyiswa ukuba ilabhoratri nganye kufuneka iseke isithuba sesalathiso sokubaluleka kwezonyango olufanelekileyo lwabemi kulo mmandla.
.Uxinaniso lwe-TT3 luphezulu kunoluhlu lwereferensi, kwaye utshintsho lwe-physiological okanye impendulo yoxinzelelo kufuneka ingabandakanywa.Ngokuqinisekileyo ingaqhelekanga, kufuneka idibanise ukuxilongwa kweempawu zeklinikhi.
.Iziphumo zale ndlela zisebenza kuphela kuluhlu lwereferensi olusekwe yile ndlela, kwaye iziphumo azifani ngokuthe ngqo 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.
I-3.I-diluent yesampuli isetyenziswa ngokukhawuleza 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 ukutshintshiselana ngeerejenti phakathi kweekhithi ezinenombolo eyahlukileyo.
.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

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:

	In Vitro Diagnostic Medical Isixhobo
	Umenzi
	Gcina kwi-2-30 ℃
	Umhla WOKUPHELELWA
	Musa Ukuphinda Usebenzise
	ISILUMKO
	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