Nnwale Ọrịa Testsea Dengue IgG/IgM Ngwa ngwa ngwa ngwa
Nkọwa ngwa ngwa
| Aha ika: | testsea | Aha ngwaahịa: | Ngwa nyocha dengue IgG/IgM |
| Ebe amụrụ: | Zhejiang, China | Ụdị: | Ngwa nyocha ọrịa pathological |
| Asambodo: | ISO9001/13485 | Nhazi akụrụngwa | Klas II |
| izi ezi: | 99.6% | Ụdị: | Serum/Plasma |
| Usoro: | Kaseti/Nwapụta | Nkọwapụta: | 3.00mm / 4.00mm |
| MOQ: | 1000 PC | Ndụ nchekwa: | afọ 2 |
Ezubere iji
Otu Nzọụkwụ Dengue IgG/IgM Test bụ ngwa ngwa chromatographic immunoassay maka nchọpụta qualitative nke ọgwụ nje (IgG na IgM) ka nje dengue na serum ma ọ bụ plasma iji nyere aka na nchoputa nke Dengue viral.ọrịa
Nchịkọta
A na-ebute Dengue site n'ata anwụnta Aedes butere nke ọ bụla n'ime dengue anọ.nje virus. Ọ na-eme n'ebe okpomọkụ na ebe okpomọkụ nke ụwa. Mgbaàmà na-apụta 3-14 ụbọchịmgbe ọrịa ahụ gasịrị. Ahụ ọkụ dengue bụ ọrịa na-efe efe nke na-emetụta ụmụ ọhụrụ, ụmụntakịrị nandị okenye. Ahụ ọkụ Dengue hemorrhagic (ọkụ ọkụ, afọ mgbu, vomiting, ọbara ọgbụgba) nwere ike imemgbagwoju anya na-egbu egbu, na-emetụta karịsịa ụmụaka. Nchọpụta mbụ nke ụlọ ọgwụ na nlezianya ụlọ ọgwụnjikwa site n'aka ndị dibịa nwere ahụmahụ na ndị nọọsụ na-abawanye ndụ nke ndị ọrịa.
Usoro ule
Kwe ka ule, ụdị, ihe nchekwa na/ma ọ bụ njikwa iru 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.
Ozi ngosi
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 kacha mma na ọnụ ahịa dị mma na-enyere anyị aka iweghara 50% nke oke ụlọ.
Usoro ngwaahịa
1. Kwadebe
2.Mkpuchi
3.Cross akpụkpọ ahụ
4.Ibe warara
5.Mgbakọ
6. Kpochie obere akpa
7.Achie akpa ahụ
8.Pack igbe
9. Ihe mkpuchi
