AFP Alpha-Fetoprotein Test Kit

Inkcazelo emfutshane:

Uvavanyo lwe-One-Step Alpha Fetoprotein (AFP) luvavanyo lwe-immunoassays lokubona amanqanaba aphezulu e-Alpha Fetoprotein (AFP) kwi-serum.Iziphumo ezisemgangathweni zifundeka lula, azifuni izixhobo ezongezelelweyo okanye ii-reagents, kwaye zimiselwa kwimizuzu eyi-10. Uxinzelelo lwe-AFP kwi-serum lusetyenziswa ngokufanelekileyo ekuncedeni ukuxilongwa kwe-hepatoma, i-ovarian, i-testicular kunye ne-presacral terato-carcinomas.

Thumela i-imeyile kuthi Khuphela njengePDF

Iinkcukacha zeMveliso

Iithegi zeMveliso

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

HIV 382

Umgaqo we-FOB Rapid Test Device

Kwi-serum, qokelela igazi kwisitya ngaphandle kwe-anticoagulant.
Vumela igazi ukuba lijike kwaye lihlukanise i-serum kwihlwili. Sebenzisa i-serum kuvavanyo.
Ukuba lo mzekelo awunakuvavanywa ngomhla wokuqokelela, gcina isampuli yeserum kwisikhenkcisi okanye kwisikhenkcisi. Yiza ne
iisampulu kubushushu begumbi ngaphambi kovavanyo. Musa ukuba ngumkhenkce kwaye unyibilikise lo mzekelo ngokuphindaphindiweyo.

HIV 382

Inkqubo yoVavanyo

1. Xa sele ulungele ukuqalisa uvavanyo, vula isingxobo esivaliweyo ngokukrazula inotshi. Susa uvavanyo kwisingxobo.

2. Dweba i-0.2ml (malunga nama-4 amaconsi) isampuli kwi-pipette, kwaye uyikhuphe kwisampuli kakuhle kwi-cassette.

3. Lindela imizuzu eyi-10-20 kwaye ufunde iziphumo. Sukuzifunda iziphumo emva kwemizuzu engama-30.

UMONGO WEKHITHI

1) Umzekelo: i-serum
2) Ifomathi: strip, ikhasethi
3) Ukukhathazeka: 25ng / ml
4) Ikiti enye ibandakanya uvavanyo lwe-1 (kunye ne-desiccant) kwisikhwama se-foil

HIV 382

UKUTOLIKWA KWEZIPHUMO

Engalunganga (-)

Ibhanti enye kuphela enemibala ibonakala kwindawo yolawulo (C). Akukho band ebonakalayo kuvavanyo (T) kummandla.

Okuhle (+)

Ukongeza kwibhendi yolawulo olunombala opinki (C), ibhendi enemibala epinki eyahlukileyo iya kuvela kwakhona kwindawo yovavanyo (T).

Oku kubonisa ukuxinwa kwe-AFP ngaphezu kwe-25ng / mL. Ukuba ibhendi yovavanyo iyalingana
ukuya okanye kumnyama kunebhendi yolawulo, ibonisa ukuba i-AFP yoxinaniso ye-specimen ifikelele

ukuya okanye kukhulu kuno 400ng/mL. Nceda udibane nogqirha wakho ukuze enze uviwo oluneenkcukacha ngakumbi.

Ayisebenzi

Ukungabikho ngokupheleleyo kombala kuyo yomibini imimandla luphawu lwempazamo yenkqubo kunye/okanye ukuba i-reagent yovavanyo iye yehla.

HIV 382

UKUGCINWA NOZINZI

Iikhithi zovavanyo zinokugcinwa kwiqondo lobushushu begumbi (18 ukuya kwi-30°C) kwisingxobo esivaliweyo ukuya kutsho kumhla wokuphelelwa kwawo.

Iikiti zovavanyo kufuneka zigcinwe kude nelanga elithe ngqo, ukufuma nobushushu.

HIV 382

Ulwazi Lomboniso

Ulwazi ngomboniso (6)

Isatifikethi sembeko

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.