Testsealabs Avian Influenza Virus Antigen Test

Testsealabs Avian Influenza Virus Antigen Nnwale egosipụtara onyonyo

Nkọwa dị mkpirikpi:

Influenza nke Avian The Vius Anigen Test bụ mpụta eruba immunochromatographic assay maka qualitative nje virus avian influenza (AVAg) na avian laryngeal ma ọ bụ cloacal secretions.

Nsonaazụ ngwa ngwa: Lab-nke ziri ezi na nkeji	Nkọwapụta nke ụlọ nyocha: Kwesịrị ntụkwasị obi na ntụkwasị obi
Nwalee ebe ọ bụla: Enweghị nleta ụlọ nyocha achọrọ	Ogo enwetara: 13485, CE, Mdsap kwadoro
Dị Mfe & Nhazi: Ọ dị mfe iji, nsogbu efu	Ọdịmma kacha mma: nwalee nke ọma n'ụlọ

Zitere anyị email Budata dị ka PDF

Nkọwa ngwaahịa

Mkpado ngwaahịa

Okwu mmalite

Nnwale nje virus nke nje virus nke Avian bụ nyocha nke immunochromatographic n'akụkụ maka nchọpụta qualitative nke nje influenza avian (AIV Ag) na larynx avian ma ọ bụ nzuzo cloaca.

Akụrụngwa

• Ihe Enyere

1.Test Cassette 2.Swab 3.Buffer 4.Package Fanye 5.Ụlọ ọrụ

Uru

Nsonaazụ doro anya	A na-ekewa bọọdụ nchọpụta ahụ ụzọ abụọ, nsonaazụ ya doro anya ma dị mfe ịgụ.
MFE	Mụta ịrụ ọrụ nkeji 1 na enweghị akụrụngwa achọrọ.
Nlele ngwa ngwa	Nkeji 10 nkeji arụpụtaghị nsonaazụ, ọ dịghị mkpa ichere ogologo oge.

Usoro ule:

微信图片_20240607142236

Ntuziaka maka ojiji

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-Ezigbo (+):Ahịrị abụọ nwere agba pụtara. Otu ahịrị kwesịrị ịpụta mgbe niile na mpaghara akara akara (C), na nke ọzọ otu ahịrị nwere agba kwesịrị ịpụta na mpaghara ahịrị ule (T).

-adịghị mma (-):Naanị otu ahịrị agba na-apụta na mpaghara akara akara (C), na enweghị ahịrị nwere agba pụtara na mpaghara ahịrị ule (T).

-adịghị mma:Enweghị ahịrị agba pụtara na mpaghara akara akara (C), na-egosi na nsonaazụ ule adịghị arụ ọrụ. Oke ihe atụ ezughi oke ma ọ bụ usoro usoro na-ezighi ezi bụ ihe kachasị kpatara ọdịda akara njikwa. N'okwu a, gụọ ntinye ngwugwu nke ọma wee jiri ngwaọrụ nnwale ọhụrụ nwalee ọzọ.

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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.