I-Tessea Disease Test Kit Dengue IgG/IgM Rapid Test Kit

Ikhithi Yokuhlola Isifo Se-Testsea I-Dengue IgG/IgM Esheshayo Esifakiwe Isithombe

Incazelo emfushane:

I gama le-brand:	testsea	Igama lomkhiqizo:	Ikhithi yokuhlola iDengue IgG/IgM
Indawo Yomsuka:	I-Zhejiang, China	Uhlobo:	Izinsiza Zokuhlaziya I-Pathological
Isitifiketi:	ISO9001/13485	Ukuhlukaniswa kwezinsimbi	Ikilasi II
Ukunemba:	99.6%	Isifanekiso:	I-Serum/Plasma
Ifomethi:	Ikhasethi/Strip	Ukucaciswa:	3.00mm/4.00mm
I-MOQ:	1000 Pcs	Impilo yeshelufu:	iminyaka engu-2

Thumela i-imeyili kithi Landa njenge-PDF

Imininingwane Yomkhiqizo

Omaka bomkhiqizo

Imininingwane Esheshayo

I gama le-brand:	testsea	Igama lomkhiqizo:	Ikhithi yokuhlola iDengue IgG/IgM
Indawo Yomsuka:	I-Zhejiang, China	Uhlobo:	Izinsiza Zokuhlaziya I-Pathological
Isitifiketi:	ISO9001/13485	Ukuhlukaniswa kwezinsimbi	Ikilasi II
Ukunemba:	99.6%	Isifanekiso:	I-Serum/Plasma
Ifomethi:	Ikhasethi/Strip	Ukucaciswa:	3.00mm/4.00mm
I-MOQ:	1000 Pcs	Impilo yeshelufu:	iminyaka engu-2

I-HIV 382

Ukusetshenziswa Okuhlosiwe

I-One Step Dengue IgG/IgM Test iyi-chromatographic immunoassay esheshayo yokutholwa kwekhwalithi yamasosha omzimba (IgG kanye ne-IgM) kugciwane lodenga ku-serum noma kuplasma ukusiza ekuxilongweni kwegciwane leDengue.ukutheleleka

I-HIV 382

Isifinyezo

Udenga lusakazwa ngokulunywa umiyane i-Aedes osutheleleke kuwo wonke ama-dengue amaneamagciwane. Kwenzeka ezindaweni ezishisayo nezishisayo emhlabeni. Izimpawu zivela ezinsukwini ezi-3-14ngemva kokulunywa okuthelelanayo. I-Dengue fever yisifo esibuhlungu esihlasela izinsana, izingane ezincane kanyeabadala. I-Dengue haemorrhagic fever (umkhuhlane, ubuhlungu besisu, ukuhlanza, ukopha) kuyinto engenzekainkinga ebulalayo, ethinta ikakhulukazi izingane. Ukuxilongwa kusenesikhathi kanye nomtholampilo ngokucophelelaukuphathwa ngodokotela abanolwazi nabahlengikazi kwandisa ukusinda kweziguli.

Inqubo Yokuhlola

Vumela ukuhlola, isifanekiso, isigcinalwazi kanye/noma izilawuli ukuthi zifinyelele izinga lokushisa legumbi elingu-15-30℃ (59-86℉) ngaphambi kokuhlolwa.

1. Letha isikhwama ekamelweni lokushisa ngaphambi kokusivula. Susa idivayisi yokuhlola ku-isikhwama esivaliwe futhi uyisebenzise ngokushesha ngangokunokwenzeka.
2. Beka idivayisi yokuhlola endaweni ehlanzekile neleveli.
3. Ngeserum noma isampula seplasma: Bamba i-dropper ngokuqondile bese udlulisela amaconsi ama-3 e-serum.noma i-plasma (cishe i-100μl) esibonelweni somthombo(S) wedivayisi yokuhlola, bese uqalaisibali sikhathi. Bheka umfanekiso ngezansi.
4. Ngezibonelo zegazi eliphelele: Bamba i-dropper ngokuqondile bese udlulisela iconsi eli-1 lelonkeigazi(cishe u-35μl) esibonelweni somthombo(S) wedivayisi yokuhlola, bese wengeza amaconsi angu-2 esibhafa (cishe u-70μl) bese uqala isibali sikhathi. Bheka umfanekiso ngezansi.
5. Linda kuze kuvele i(ama)layini anombala. Funda imiphumela ngemizuzu eyi-15. Ungatoliki iumphumela ngemva kwemizuzu engu-20.

Ukusebenzisa inani elanele lesifanekiso kubalulekile ukuze uthole umphumela wokuhlola ovumelekile. Uma ukufuduka (i-wettingye-membrane) ayibonwa efasiteleni lokuhlola ngemva komzuzu owodwa, engeza ithonsi elilodwa lebhafa(yegazi eliphelele) noma isifanekiso (seserum noma iplasma) emthonjeni wesifanekiso.

Ukuhunyushwa Kwemiphumela

Okuhle:Kuvela imigqa emibili. Umugqa owodwa kufanele uvele njalo endaweni yomugqa wokulawula(C), kanyeomunye umugqa onombala obonakalayo kufanele uvele endaweni yomugqa wokuhlola.

Okubi:Umugqa owodwa onombala uvela endaweni yokulawula(C).Awukho umugqa onombala obonakalayo ovelayoisifunda somugqa wokuhlola.

Okungavumelekile:Ulayini wokulawula uyehluleka ukuvela. Ivolumu yesampula enganele noma inqubo engalungileamasu yizizathu okungenzeka kakhulu zokwehluleka komugqa wokulawula.

★ Buyekeza inqubo bese uphindaukuhlola ngedivayisi yokuhlola entsha. Uma inkinga iqhubeka, yeka ukusebenzisa ikhithi yokuhlola ngokushesha futhi uxhumane nomsabalalisi wangakini.

Ulwazi Lombukiso

Ulwazi Lombukiso (6)

Isitifiketi Sokuhlonishwa

Iphrofayela Yenkampani

Thina, i-Hangzhou Testsea Biotechnology Co., Ltd yinkampani ekhula ngokushesha yobuchwephesha be-biotechnology ekhethekile ekucwaningeni, ekuthuthukiseni, ekukhiqizeni nasekusabalaliseni amakhithi okuhlola e-in-vitro diagnostic(IVD) athuthukile namathuluzi ezokwelapha.
Indawo yethu yi-GMP, ISO9001, kanye ne-ISO13458 futhi sinemvume ye-CE FDA. Manje sesibheke ngabomvu ukubambisana nezinye izinkampani zaphesheya ukuze sithuthukiselane.
Sikhiqiza ukuhlolwa kwenzalo, ukuhlolwa kwezifo ezithathelwanayo, ukuhlola ukusetshenziswa kabi kwezidakamizwa, ukuhlola umaka wenhliziyo, ukuhlolwa komaka isimila, ukuhlolwa kokudla nokuphepha kanye nokuhlolwa kwezifo zezilwane, ngaphezu kwalokho, uhlobo lwethu lwe-TESTSEALABS lwaziwa kakhulu ezimakethe zasekhaya neziphesheya kwezilwandle. Izinga eliphezulu nezintengo ezivumayo zisenza sikwazi ukuthatha amasheya asekhaya angaphezu kuka-50%.