中文名稱：NDUFAF1 抗原（重組蛋白）

英文名稱：NDUFAF1 Antigen (Recombinant Protein)

別名：NADH dehydrogenase (ubiquinone) complex I, assembly factor 1; CGI65; CIA30; CGI-65

儲存：冷凍（-20℃）

相關(guān)類別：抗原

概述

Fusion protein corresponding to a region derived from 25-327 amino acids of human NDUFAF1

技術(shù)規(guī)格

Full name:

NADH dehydrogenase (ubiquinone) complex I, assembly factor 1

Synonyms:

CGI65; CIA30; CGI-65

Swissprot:

Q9Y375

Gene Accession:

BC000780

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 complex I assembly factor protein. Complex I (NADH-ubiquinone oxidoreductase) catalyzes the transfer of electrons from NADH to ubiquinone (coenzyme Q) in the first step of the mitochondrial respiratory chain, resulting in the translocation of protons across the inner mitochondrial membrane. The encoded protein is required for assembly of complex I, and mutations in this gene are a cause of mitochondrial complex I deficiency. Alternatively spliced transcript variants have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 19.

021-54845833/15800441009

ELISA試劑盒

PCR試劑盒

生化試劑盒

農(nóng)殘檢測試劑盒

細(xì)胞庫

基礎(chǔ)培養(yǎng)基

完全培養(yǎng)基

原代細(xì)胞

細(xì)胞專用培養(yǎng)基

細(xì)胞系

菌株

生化試劑

病理染色液

科研抗體

標(biāo)準(zhǔn)品

血清

形態(tài)病理檢測

分子病理

超微病理

細(xì)胞凋亡與檢測

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相關(guān)文章

DUFAF1 抗原（重組蛋白）

Full name:	NADH dehydrogenase (ubiquinone) complex I, assembly factor 1
Synonyms:	CGI65; CIA30; CGI-65
Swissprot:	Q9Y375
Gene Accession:	BC000780
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 complex I assembly factor protein. Complex I (NADH-ubiquinone oxidoreductase) catalyzes the transfer of electrons from NADH to ubiquinone (coenzyme Q) in the first step of the mitochondrial respiratory chain, resulting in the translocation of protons across the inner mitochondrial membrane. The encoded protein is required for assembly of complex I, and mutations in this gene are a cause of mitochondrial complex I deficiency. Alternatively spliced transcript variants have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 19.