ACAA1 (27-424, His-tag)

CAT#: AR09612PU-L

Recombinant human ACAA1 protein, fused to His-tag at N-terminus, was expressed in E.coli and purified by using conventional chromatography techniques.

Product images

Specifications

Product Data

• Description: Recombinant human ACAA1 protein, fused to His-tag at N-terminus, was expressed in E.coli and purified by using conventional chromatography techniques.
• Species: Human
• Expression Host: E.Coli
• Expression cDNA Clone or AA Sequence: MGSSHHHHHH SSGLVPRGSH MLSGAPQASA ADVVVVHGRR TAICRAGRGG FKDTTPDELL SAVMTAVLKD VNLRPEQLGD ICVGNVLQPG AGAIMARIAQ FLSDIPETVP LSTVNRQCSS GLQAVASIAG GIRNGSYDIG MACGVESMSL ADRGNPGNIT SRLMEKEKAR DCLIPMGITS ENVAERFGIS REKQDTFALA SQQKAARAQS KGCFQAEIVP VTTTVHDDKG TKRSITVTQD EGIRPSTTME GLAKLKPAFK KDGSTTAGNS SQVSDGAAAI LLARRSKAEE LGLPILGVLR SYAVVGVPPD IMGIGPAYAI PVALQKAGLT VSDVDIFEIN EAFASQAAYC VEKLRLPPEK VNPLGGAVAL GHPLGCTGAR QVITLLNELK RRGKRAYGVV SMCIGTGMGA AAVFEYPGN
• Tag: His-tag
• Predicted MW: 43.8 kDa
• Concentration: 1.0 mg/ml (determined by Bradford assay)
• Purity: > 95 % by SDS – PAGE
• Buffer: 20 mM Tris-HCl buffer (pH 8.0) containing 10% glycerol, 1 mM DTT, 0.1 M NaCl
• Preparation: Liquid purified protein

Reference Data

• RefSeq: NP_001123882
• Locus ID: 30
• Cytogenetics: 3p22.2
• Synonyms: ACAA; PTHIO; THIO
• Summary: This gene encodes an enzyme operative in the beta-oxidation system of the peroxisomes. Deficiency of this enzyme leads to pseudo-Zellweger syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]
• Protein Pathways: Fatty acid metabolism, Valine, leucine and isoleucine degradation, Biosynthesis of unsaturated fatty acids, Metabolic pathways, PPAR signaling pathway