CEA Carcinoembryonic Antigen Test Kit
Itheyibhile yeParameter
Inombolo yoMzekelo | I-TSIN101 |
Igama | AFP Alpha-Fetoprotein Test Kit |
Iimbonakalo | Uvakalelo oluphezulu, lulula, lulula kwaye luchanekile |
Umzekelo | WB/S/P |
Inkcazo | 3.0mm 4.0mm |
Ukuchaneka | 99.6% |
Ugcino | 2'C-30'C |
Ukuhambisa ngenqanawe | Ngolwandle/Ngomoya/TNT/Fedx/DHL |
Ukuhlelwa kwesixhobo | Udidi II |
Isatifikethi | CE ISO FSC |
Beka ubomi kwishelufa | iminyaka emibini |
Uhlobo | Izixhobo zokuHlalutya kwePathological |
Umgaqo we-FOB Rapid Test Device
Isixhobo soVavanyo oluKhawulezayo lwe-CEA (igazi elipheleleyo / iSerum / iPlasma) yenzelwe ukufumana i-antigen ye-carcinoembryonic antigen (CEA) ngokuchazwa okubonakalayo kokuphuhliswa kombala kumgca wangaphakathi. I-membrane yayingashukumi kunye ne-anti-CEA yokubamba izilwa-buhlungu kwindawo yovavanyo. Ngexesha lovavanyo, umzekelo uvumelekile ukuba usabele nge-anti-CEA enemibala ye-monoclonal antibodies colloidal conjugates yegolide, eyayifakwe ngaphambili kwisampula yovavanyo. Emva koko umxube uhamba kwi-membrane ngesenzo se-capillary, kwaye udibanise nama-reagents kwi-membrane. Ukuba bekukho i-CEA eyaneleyo kwimizekelo, ibhendi enemibala iya kwenza kwindawo yokuvavanya kwi-membrane. Ubukho beli bhanti elinemibala libonisa umphumo omuhle, ngelixa ukungabikho kwawo kubonisa umphumo ombi. Ukubonakala kwebhanti enemibala kwindawo yokulawula isebenza njengolawulo lwenkqubo. Oku kubonisa ukuba umthamo ofanelekileyo we-specimen wongeziwe kwaye i-membrane wicking yenzeke.
1.Musa ukuvula isingxobo sefoil de ulungele ukuqalisa uvavanyo. Izixhobo zovavanyo ezifakwe efrijini kufuneka zivunyelwe ukuba zize kubushushu begumbi (15°-28°C) phambi kokuba uvule isingxobo.
2. Susa isixhobo kwisingxobo sokhuselo uze uleyibhelishe isixhobo ngophawu lomfanekiso.
3. Yongeza i-50 ul yegazi elitsha kwiSample Well (yeKhadi) okanye iSample Pad (yeDipstick), uze udibanise ama-2 amathontsi (50 ul) ovavanyo oluqhuba isithinteli kwisampulu yesampulu okanye iphedi yesampula.
4. Funda isiphumo kwi-10-15 imizuzu. Sukuzifunda iziphumo emva kwemizuzu eli-15. Qwalasela
ibhendi enemibala ephuhliswe phezu kommandla wolawulo ebonisa ukuba uvavanyo lugqityiwe.
Inkqubo yoVavanyo
UMONGO WEKHITHI
1.Izixhobo zovavanyo ezipakishwe ngumntu ngamnye
Isixhobo ngasinye siqulethe i-strip ene-conjugates enemibala kunye nee-reagents ezisebenzayo ezisasazwe kwangaphambili kwiindawo ezihambelanayo.
2.Iipayipi ezilahlayo
Ukongeza imizekelo sebenzisa.
3.Isithinteli
I-phosphate buffered saline kunye nepreservative.
4.Faka iphakheji
Ngomyalelo wokusebenza.
UKUTOLIKWA KWEZIPHUMO
Okuhle (+)
Amabhanti amabini apinki avela kwindawo yovavanyo. Oku kubonisa ukuba lo mzekelo uneCEA
Engalunganga (-)
Linye kuphela iqela elipinki elivela kummandla wovavanyo. Oku kubonisa ukuba akukho CEA kulo lonke igazi.
Ayisebenzi
Ukuba ngaphandle kwebhendi enemibala ibonakala kwindawo yokuvavanya, oku kubonisa impazamo enokwenzeka ekwenzeni uvavanyo. Uvavanyo kufuneka luphindwe kusetyenziswa isixhobo esitsha.
Ulwazi Lomboniso
Iprofayile yekhampani
Thina, i-Hangzhou Testsea Biotechnology Co., Ltd yinkampani ekhula ngokukhawuleza yobuchwephesha bebhayoloji ekhethekileyo ekuphandeni, ekuphuhliseni, ekuveliseni nasekusasazeni iikhithi zovavanyo lwe-in-vitro diagnostic (IVD) kunye nezixhobo zonyango.
Indawo yethu yi-GMP, ISO9001, kunye ne-ISO13458 eqinisekisiweyo kwaye sinemvume ye-CE FDA. Ngoku sijonge phambili ekusebenzisaneni neenkampani zaphesheya kwezilwandle ngophuhliso olufanayo.
Sivelisa uvavanyo lokuchuma, uvavanyo lwezifo ezosulelayo, uvavanyo lokusetyenziswa kakubi kweziyobisi, uvavanyo lwentliziyo, uvavanyo lokumakisha ithumba, uvavanyo lokutya kunye nokhuseleko kunye novavanyo lwezifo zezilwanyana, ukongezelela, uphawu lwethu lwe-TESTSEALABS luye lwaziwa kakhulu kwiimarike zasekhaya naphesheya. Umgangatho ogqwesileyo kunye namaxabiso ancomekayo asenza sikwazi ukuthatha ngaphezulu kwe-50% yezabelo zasekhaya.
Inkqubo yeMveliso
1.Lungiselela
2.Ikhava
3.Inwebu enqamlezileyo
4.Sika umcu
5.Indibano
6.Pakisha iipowutshi
7.Zitywine iingxowa
8.Pakisha ibhokisi
9.Encasement