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  • 產品名稱:NDUFS7 抗原(重組蛋白)

  • 產品型號:100ug
  • 產品廠商:通蔚生物
  • 產品價格:800
  • 產品庫存:35
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我司專業經銷生命科學領域NDUFS7 抗原(重組蛋白),有著豐富服務經驗和深厚專業背景的團隊為您提供技術服務和支持,各種標本、種屬、具體指標齊全,檢測范圍以及試劑盒內容及其配制,我們努力的腳步不會就此停息,我們的成績離不開廣大新老客戶的支持與厚愛,在未來的一年里,我們將更加努力,用上等的產品與誠摯的服務回饋廣大用戶!
詳情介紹:



中文名稱: NDUFS7 抗原(重組蛋白)

英文名稱: NDUFS7 Antigen (Recombinant Protein)

別     名:  NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Q reductase); PSST; CI-20; MY017; CI-20KD

儲     存:  冷凍(-20℃)

相關類別: 抗原

概     述

Fusion protein corresponding to a region derived from 39-213 amino acids of human NDUFS7

技術規格

Full name:

NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Q reductase)

Synonyms:

PSST; CI-20; MY017; CI-20KD

Swissprot:

O75251

Gene Accession:

BC005954

Purity:

>85%, as determined by Coomassie blue stained SDS-PAGE

Expression system:

Escherichia coli

Tags:

His tag C-Terminus, GST tag N-Terminus

Background:

This gene encodes a protein that is a subunit of one of the complexes that forms the mitochondrial respiratory chain. This protein is one of over 40 subunits found in complex I, the nicotinamide adenine dinucleotide (NADH):ubiquinone oxidoreductase. This complex functions in the transfer of electrons from NADH to the respiratory chain, and ubiquinone is believed to be the immediate electron acceptor for the enzyme. Mutations in this gene cause Leigh syndrome due to mitochondrial complex I deficiency, a severe neurological disorder that results in bilaterally symmetrical necrotic lesions in subcortical brain regions.





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