Quick Order of raPOOL for HSD17B10

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Official Symbol:	HSD17B10
NCBI Gene ID:	3028
Aliases:	17b-HSD10 ABAD CAMR DUPXp11.22 ERAB HADH2 HCD2 HSD10MD MHBD MRPP2 MRX17 MRX31 MRXS10 SCHAD SDR5C1
Official Full Name:	hydroxysteroid 17-beta dehydrogenase 10
Species:	human
Summary:	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 and steroids, and is a subunit of mitochondrial ribonuclease P, which is involved in tRNA maturation. The protein has been implicated in the development of Alzheimer disease, and mutations in the gene are the cause of 17beta-hydroxysteroid dehydrogenase type 10 (HSD10) deficiency. Several alternatively spliced transcript variants have been identified, but the full-length nature of only two transcript variants has been determined. [provided by RefSeq, Aug 2014].

 

Buy raPOOLs for HSD17B10

There is no existing raPOOL for your gene, hence a custom raPOOL set up service is required. Please add this to cart and proceed to choose the raPOOL scale required where 2, 5 or 10 nmol is sufficient for 20, 50 or 100 reactions with the recommended use of 100 pmol raPOOL per reaction.