AFP Alpha-Fetoprotein 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
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.
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
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.
UKUGCINWA NOZINZI
Iikiti 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.
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