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  • COX10抗原(重組蛋白)

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    • 品牌 : 通蔚生物
    • 目錄號(hào) : TW10198
    • 應(yīng)用 : 僅供科研使用
    • 保存條件 : 低溫保存
    • 貨期 : 現(xiàn)貨
    • 商品庫(kù)存:75
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中文名稱:COX10抗原(重組蛋白)

英文名稱:
COX10 Antigen (Recombinant Protein)

儲(chǔ)      存:
冷凍(-20℃)

相關(guān)類別:抗原

概述

Fusion protein corresponding to N terminal 300 amino acids of human COX10


技術(shù)規(guī)格

Full name:

COX10 homolog, cytochrome c oxidase assembly protein, heme A: farnesyltransferase

Swissprot:

Q12887

Gene Accession:

BC000060

Purity:

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

Expression system:

Escherichia coli

Tags:

His tag C-Terminus, GST tag N-Terminus

Background:

Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes heme A:farnesyltransferase, which is not a structural subunit but required for the expression of functional COX and functions in the maturation of the heme A prosthetic group of COX. This protein is predicted to contain 7-9 transmembrane domains localized in the mitochondrial inner membrane. A gene mutation, which results in the substitution of a lysine for an asparagine (N204K), is identified to be responsible for cytochrome c oxidase deficiency. In addition, this gene is disrupted in patients with CMT1A (Charcot-Marie-Tooth type 1A) duplication and with HNPP (hereditary neuropathy with liability to pressure palsies) deletion.


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