Nnwale Ọrịa Testsea TOXO IgG/IgM Ngwa ngwa ngwa ngwa

Nnwale Ọrịa Testsea TOXO IgG/IgM Ngwa ngwa ngwa egosipụtara onyonyo

Nkọwa dị mkpirikpi:

Aha ika:	testsea	Aha ngwaahịa:	Ngwa ngwa ule TOXO IgG/IgM
Ebe amụrụ:	Zhejiang, China	Ụdị:	Ngwa nyocha ọrịa pathological
Asambodo:	ISO9001/13485	Nhazi akụrụngwa	Klas II
izi ezi:	99.6%	Ụdị:	Ọbara dum/Serum/Plasma
Usoro:	Kaseti/Nwapụta	Nkọwapụta:	3.00mm / 4.00mm
MOQ:	1000 PC	Ndụ nchekwa:	afọ 2

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Nkọwa ngwaahịa

Mkpado ngwaahịa

Nkọwa ngwa ngwa

Aha ika:	testsea	Aha ngwaahịa:	Ngwa ngwa ule TOXO IgG/IgM
Ebe amụrụ:	Zhejiang, China	Ụdị:	Ngwa nyocha ọrịa pathological
Asambodo:	ISO9001/13485	Nhazi akụrụngwa	Klas II
izi ezi:	99.6%	Ụdị:	Ọbara dum/Serum/Plasma
Usoro:	Kaseti/Nwapụta	Nkọwapụta:	3.00mm / 4.00mm
MOQ:	1000 PC	Ndụ nchekwa:	afọ 2

HIV 382

Ezubere iji

Toxo igg/igm Rpid Test bụ ule immunochromatographic ngwa ngwa maka nchọpụta otu oge nke ọgwụ mgbochi IgM na IgG.Toxo gondiina mmadụ serum/plasma.Enwere ike iji ule ahụ dị ka nyocha nyocha maka ọrịa Toxo yana enyemaka maka nchọpụta dị iche iche nke na-amachi onwe ya ọrịa Toxo isi na ọrịa Toxo nke abụọ nwere ike ịnwụ na njikọ ndị ọzọ.

HIV 382

Nchịkọta

Nnwale ngwa ngwa Toxo IgG/IgM bụ immunoassay chromatographic nke mpụta.Kaseti ule ahụ nwere: 1) pad conjugate na-acha agba burgundy nwere Toxo recombinant envelopu antigens conjugated na colloid gold (Toxo conjugates) na oke bekee IgG-gold conjugates,2) nitrocellulose akpụkpọ anụ eriri nwere ule abụọ (T1 na T2 bands) na otu njikwa njikwa (C band).A na-eji ihe mgbochi kpuchie T1 band maka nchọpụta IgM anti-Toxo, T2 band a na-ekpuchi ya na mgbochi maka nchọpụta IgG anti-Toxo, na C band ejiri ewu mgbochi oke bekee IgG kpuchie ya.Mgbe a na-ekesa oke nlere ule zuru oke n'ime olulu mmiri nlele nke cassette, ihe nlere ahụ na-akwaga site na capillary edinam gafee cassette.A na-ejide immunocomplex ahụ site na reagent mkpuchi mkpuchi na T2 band, na-eme otu band T2 nwere agba burgundy, na-egosi nsonaazụ Toxo IgG dị mma ma na-atụ aro ọrịa na-adịbeghị anya ma ọ bụ megharịa.A na-ejide immunocomplex ahụ site na reagent kpuchiri ya na band T1, na-akpụ otu band T1 nwere agba burgundy, na-egosi nsonaazụ Toxo IgM dị mma ma na-atụ aro ọrịa ọhụrụ.Enweghị ụdọ T ọ bụla (T1 na T2) na-egosi nsonaazụ na-adịghị mma.

Usoro ule

Kwe ka ule, ụdị, ihe nchekwa na/ma ọ bụ njikwa rute ọnụ ụlọ okpomọkụ 15-30℃ (59-86℉) tupu nnwale.

1. Weta obere akpa ahụ na okpomọkụ tupu imeghe ya.Wepu ngwaọrụ nnwale naobere akpa akara ma jiri ya ozugbo enwere ike.
2. Debe ngwaọrụ ule na elu dị ọcha na larịị.
3. Maka ụdị serum ma ọ bụ plasma: Jide dropper ahụ kwụ ọtọ ma bufee mmiri mmiri 3.ma ọ bụ plasma (ihe dị ka 100μl) gaa na ụdị nke ọma (S) nke ngwaọrụ nnwale, wee malitengụ oge.Lee ihe atụ n'okpuru.
4. Maka ụdị ọbara zuru oke: Jide ntụpọ ahụ kwụ ọtọ ma bufee 1 dobe nke dumọbara (ihe dị ka 35μl) na ụdị nke ọma (S) nke ngwaọrụ nnwale, wee tinye 2 tụlee nke ihe nchekwa (ihe dị ka 70μl) wee malite ngụ oge.Lee ihe atụ n'okpuru.
5. Chere ka ahịrị(s) nwere agba pụta.Gụọ nsonaazụ na nkeji iri na ise.Atụgharịla yapụta mgbe 20 nkeji.

Itinye ihe nlere zuru oke dị mkpa maka nsonaazụ ule dị mma.Ọ bụrụ na mbugharị (wettingA naghị ahụ nke akpụkpọ ahụ) na windo ule mgbe otu nkeji gachara, tinye otu dobe nchekwa ọzọ(maka ọbara zuru oke) ma ọ bụ ụdị (maka serum ma ọ bụ plasma) na ihe nlele ahụ nke ọma.

Nkọwa nke nsonaazụ

Nke dị mma:Ahịrị abụọ pụtara.Otu ahịrị kwesịrị ịpụta mgbe niile na mpaghara akara akara (C), naọzọ otu doro anya na-acha ahịrị kwesịrị ịpụta na mpaghara ahịrị ule.

adịghị mma:Otu ahịrị na-acha na-egosi na mpaghara njikwa(C).Ọnweghị ahịrị agba pụtara ìhè pụtarampaghara akara ule.

Na ezighi ezi:Ahịrị njikwa agaghị apụta.Oke ihe atụ ezughi oke ma ọ bụ usoro ezighi eziusoro bụ ihe yikarịrị kpatara ọdịda akara akara.

★ Nyochaa usoro ma kwugharịaule na ngwaọrụ ule ọhụrụ.Ọ bụrụ na nsogbu ahụ dịgidere, kwụsị iji ngwa nnwale ozugbo wee kpọtụrụ onye nkesa mpaghara gị.

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Asambodo nsọpụrụ

Nkọwapụta Ụlọ ọrụ

Anyị, Hangzhou Testsea Biotechnology Co., Ltd bụ ụlọ ọrụ ọkachamara biotechnology na-eto ngwa ngwa ọkachamara na nyocha, mmepe, nrụpụta na nkesa nke ngwa ule in-vitro diagnostics (IVD) dị elu na ngwa ahụike.
Ụlọ ọrụ anyị bụ GMP, ISO9001, na ISO13458 kwadoro ma anyị nwere nkwenye CE FDA.Ugbu a, anyị na-atụ anya isonyere ọtụtụ ụlọ ọrụ esenidụt maka mmepe otu.
Anyị na-emepụta ule ọmụmụ, ule ọrịa na-efe efe, ule iji ọgwụ ọjọọ eme ihe, ule akara obi, ule akara tumor, ule nri na nchekwa na ule ọrịa anụmanụ, na mgbakwunye, akara TESTSEALABS bụ nke ama ama n'ahịa ụlọ na mba ofesi.Ogo kachasị mma na ọnụ ahịa dị mma na-enyere anyị aka iweghara 50% nke oke ụlọ.