Uvavanyo lweSifo seTestsea kwiChlamydia Pneumoniae Ab IgM eKhawulezayo yoVavanyo lweKit
Iinkcukacha eziKhawulezayo
| Igama lebrand: | testsea | Igama lemveliso: | Chlamydia Pneumoniae Ab IgM Rapid Test Kit |
| Indawo yemvelaphi: | Zhejiang, China | Uhlobo: | Izixhobo zokuHlalutya kwePathological |
| Isatifikethi: | ISO9001/13485 | Ukuhlelwa kwesixhobo | Udidi II |
| Ukuchaneka: | 99.6% | Umzekelo: | Igazi elipheleleyo/iSerum/Plasma |
| Ubume: | Ikhasethi/Strip | Inkcazo: | 3.00mm/4.00mm |
| MOQ: | 1000 iiPC | Beka ubomi kwishelufa: | iminyaka eyi-2 |
Ukusetyenziswa okucetywayo
Uvavanyo oluKhawulezayo lwe-CP-IgM luvavanyo lwe-chromatographic olukhawulezayo lokukhangela umgangatho we-antibodies (IgM) ukuya kwi-chlamydia pneumoniae kwi-Whole Blood/Serum/Plasma ukunceda ekuxilongweni kweChlamydia pneumoniae virus.
Inkqubo yoVavanyo
Vumela uvavanyo, umfuziselo, isithinteli kunye/okanye ulawulo lufikelele kubushushu begumbi 15-30℃ (59-86℉) phambi kovavanyo.
1. Zisa isingxobo kwiqondo lobushushu begumbi phambi kokuba usivule. Susa isixhobo sovavanyo kwiisingxobo esitywiniweyo kwaye uyisebenzise ngokukhawuleza.
2. Beka isixhobo sokuvavanya kwindawo ecocekileyo kunye nenqanaba.
3. Kwi-serum okanye isampuli yeplasma: Bamba idropha ngokuthe nkqo kwaye udlulisele amathontsi ama-3 eserum.okanye iplasma (malunga ne-100μl) kumzekelo wequla (S) lesixhobo sovavanyo, emva koko uqaliseisibali-xesha. Jonga umfanekiso ongezantsi.
4. Kwimizekelo yegazi elipheleleyo: Bamba idropha ngokuthe nkqo kwaye udlulisele ithontsi eli-1 elipheleleyoigazi (malunga ne-35μl) kumzekelo kakuhle (S) wesixhobo sovavanyo, uze udibanise amathontsi ama-2 e-buffer (malunga ne-70μl) kwaye uqalise isibali-xesha. Jonga umfanekiso ongezantsi.
5. Lindela ukuba kuvele umgca onemibala. Funda iziphumo ngemizuzu eyi-15. Musa ukuyitolika iiziphumo emva kwemizuzu engama-20.
Ukusebenzisa isixa esaneleyo somzekelo kubalulekile kwisiphumo sovavanyo esisebenzayo. Ukuba ukufuduka (ukumanzisaye-membrane) ayijongwa kwifestile yovavanyo emva komzuzu omnye, yongeza enye ithontsi ye-buffer(yegazi elipheleleyo) okanye isampuli (yeserum okanye iplasma) kumfanekiso wequla.
Ukutolikwa kweziPhumo
Okuhle:Kuvela imigca emibini. Umgca omnye kufuneka uhlale ubonakala kwingingqi yolawulo (C), kunyeomnye umgca wombala ocacileyo kufuneka uvele kwindawo yovavanyo.
Engalunganga:Umgca omnye onemibala uvela kummandla wolawulo (C).Akukho mgca wombala obonakalayo ovelayoummandla wovavanyo.
Ayisebenzi:Umgca wolawulo uyasilela ukubonakala. Umthamo wesampuli enganelanga okanye inkqubo engachanekangaubuchule zezona zizathu zinokwenzeka zokusilela komgca wolawulo.
★ Hlaziya inkqubo kwaye uphindeuvavanyo ngesixhobo esitsha sovavanyo. Ukuba ingxaki iyaqhubeka, yeka ukusebenzisa ikiti yovavanyo ngoko nangoko kwaye uqhagamshelane nomsasazi wakho wendawo.
Ulwazi Lomboniso
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.
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
