重组17-β-羟基类固醇脱氢酶10(HSD17b10)蛋白

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重组内质网Aβ相关结合蛋白
Recombinant HSD17B10

基因名：

HSD17B10

产品别名：

17b-HSD10； ABAD； CAMR； DUPXp11.22； ERAB； HADH2； HCD2； HSD10MD； MHBD； MRPP2； MRX17； MRX31； MRXS10； SCHAD； SDR5C1； HSD17B10； hydroxysteroid 17-beta dehydrogenase 10； hydroxysteroid 17-beta dehydrogenase 10； 3-hydroxyacyl-CoA dehydrogenase type-2； 3-hydroxy-2-methylbutyryl-CoA dehydrogenase； AB-binding alcohol dehydrogenase； amyloid-beta peptide binding alcohol dehydrogenase； endoplasmic reticulum-associated amyloid beta-peptide-binding protein； mitochondrial RNase P subunit 2； mitochondrial ribonuclease P protein 2； short chain L-3-hydroxyacyl-CoA dehydrogenase type 2； short chain type dehydrogenase/reductase XH98G2； 17-β-羟基类固醇脱氢酶10(HSD17b10)；内质网Aβ相关结合蛋白；

背景信息：

This gene encodes 3-hydroxyacyl-CoA dehydrogenase type II, a member of the short-chain dehydrogenase/reductase superfamily. The gene product is a mitochondrial protein that catalyzes the oxidation of a wide variety of fatty acids, alcohols, and steroids. The protein has been implicated in the development of Alzheimer's disease, and mutations in the gene are the cause of 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency (MHBD). Several alternatively spliced transcript variants have been identified, but the full-length nature of only two transcript variants has been determined. [provided by RefSeq, Jul 2008].