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  • DLAT 抗原(重組蛋白)

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    • 品牌 : 通蔚生物
    • 目錄號(hào) : TW4421
    • 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:20
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中文名稱(chēng):DLAT 抗原(重組蛋白)

英文名稱(chēng):DLAT Antigen (Recombinant Protein)

別     名: dihydrolipoamide S-acetyltransferase; DLTA; PDCE2; PDC-E2

儲(chǔ)     存: 冷凍(-20℃)

相關(guān)類(lèi)別:抗原

概     述

Fusion protein corresponding to C terminal 200 amino acids of human DLAT

技術(shù)規(guī)格

Full name:

dihydrolipoamide S-acetyltransferase

Synonyms:

DLTA; PDCE2; PDC-E2

Swissprot:

P10515

Gene Accession:

BC039084

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 component E2 of the multi-enzyme pyruvate dehydrogenase complex (PDC). PDC resides in the inner mitochondrial membrane and catalyzes the conversion of pyruvate to acetyl coenzyme A. The protein product of this gene, dihydrolipoamide acetyltransferase, accepts acetyl groups formed by the oxidative decarboxylation of pyruvate and transfers them to coenzyme A. Dihydrolipoamide acetyltransferase is the antigen for antimitochondrial antibodies. These autoantibodies are present in nearly 95% of patients with the autoimmune liver disease primary biliary cirrhosis (PBC). In PBC, activated T lymphocytes attack and destroy epithelial cells in the bile duct where this protein is abnormally distributed and overexpressed. PBC enventually leads to cirrhosis and liver failure. Mutations in this gene are also a cause of pyruvate dehydrogenase E2 deficiency which causes primary lactic acidosis in infancy and early childhood.