I-Tessea Disease Test TYP Typhoid IgG/IgM Rapid Test Kit

Ukuhlolwa Kwesifo Se-Tessea I-TYP Typhoid IgG/IgM Rapid Test Kit Isithombe Esifakiwe

Incazelo emfushane:

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

I-HIV 382

Ukusetshenziswa Okuhlosiwe

I-Typhoid IgG/IgM Rapid Test iyi-lateral flow immunoassay yokutholwa kanye nokuhlukaniswa ngesikhathi esisodwa kwe-anti-Salmonella typhi (S. typhi) IgG ne-IgM ku-serum yomuntu, i-plasma. Kuhloswe ukuthi kusetshenziswe njengokuhlola ukuhlola futhi njengosizo ekuxilongeni ukutheleleka nge-S. typhi. Noma yisiphi isifanekiso esisebenzayo esine-Typhoid IgG/IgM Rapid Test kufanele siqinisekiswe ngezinye izindlela zokuhlola.

I-HIV 382

Isifinyezo

I-typhoid fever ibangelwa i-S. typhi, igciwane le-Gram-negative. Emhlabeni jikelele zilinganiselwa ezigidini eziyi-17 izehlakalo kanye nokufa okuhlobene nezi-600,000 kwenzeka ngonyaka1. Iziguli ezitheleleke nge-HIV zisengozini enkulu kakhulu yokutheleleka nge-S. typhi2. Ubufakazi bokutheleleka nge-H. pylori bubuye buveze ingozi eyengeziwe yokuthola i-typhoid fever. I-1-5% yeziguli iba umthwali wezifo ezingelapheki ophethe i-S. typhi kunyongo.

Ukuxilongwa komtholampilo kwe-typhoid fever kuncike ekuhlukaniseni kwe-S. typhi egazini, umnkantsha noma isilonda esithile se-anatomic. Ezikhungweni ezingakwazi ukwenza le nqubo eyinkimbinkimbi futhi edla isikhathi, ukuhlolwa kwe-Filix-Widal kusetshenziselwa ukusiza ukuxilongwa. Kodwa-ke, ukulinganiselwa okuningi kuholela ebunzimeni ekuchazeni ukuhlolwa kwe-Widal3,4.

Ngokuphambene, iTyphoid IgG/IgM Rapid Test iwukuhlolwa kwaselabhorethri okulula futhi okusheshayo. Ukuhlola kanyekanye kuthola futhi kwehlukanise amasosha omzimba e-IgG kanye ne-IgM ku-S. typhi ethize antigen5 t kusampula yegazi lonke ngaleyo ndlela kusize ekunqumeni ukuchayeka kwamanje noma kwangaphambilini ku-S. typhi.

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%.