KD-Validated HSD17B10 Mouse Monoclonal Antibody

Description

EnkiLife offers the KD-Validated HSD17B10 Mouse Monoclonal Antibody. This antibody reacts with Human and is suitable for WB,FCM,ICC application. The product boasts remarkable high specificity, outstanding reproducibility, and exceptional affinity, making it a reliable and superior choice for your needs. Dilution Ratio: WB 1:500-1:2,500; FC 1:200-1:2,000; ICC 1:100-1:1,000 Alternative Names of Immunogen:HSD17B10; Hydroxysteroid 17-Beta Dehydrogenase 10; SDR5C1; MRPP2; ERAB; MHBD; 17b-HSD10; HADH2; ABAD; CAMR; Endoplasmic Reticulum-Associated Amyloid Beta-Peptide-Binding Protein; 3-Hydroxy-2-Methylbutyryl-CoA Dehydrogenase; 3-Hydroxyacyl-CoA Dehydrogenase Type-2; Mitochondrial Ribonuclease P Protein 2; AB-Binding Alcohol Dehydrogenase; Mitochondrial RNase P Subunit 2; MRXS10; SCHAD; Hydroxyacyl-Coenzyme A Dehydrogenase, Type II, Hydroxyacyl-Coenzyme A Dehydrogenase, Type II; Short Chain Dehydrogenase/Reductase Family 5C, Member 1; 3-Alpha-(17-Beta)-Hydroxysteroid Dehydrogenase (NAD(+)); Short Chain Dehydrogenase/Reductase Family 5C Member 1; Short Chain L-3-Hydroxyacyl-CoA Dehydrogenase Type 2; Amyloid-Beta Peptide Binding Alcohol Dehydrogenase; Short Chain Type Dehydrogenase/Reductase XH98G2; Short-Chain Type Dehydrogenase/Reductase XH98G2; 3alpha(Or 20beta)-Hydroxysteroid Dehydrogenase; Type 10 17beta-Hydroxysteroid Dehydrogenase; 2-Methyl-3-Hydroxybutyryl-CoA Dehydrogenase; Mental Retardation, X-Linked, Syndromic 10; Hydroxysteroid (17-Beta) Dehydrogenase 10; 3-Hydroxyacyl-CoA Dehydrogenase Type II; 7-Alpha-Hydroxysteroid Dehydrogenase; 17-Beta-Estradiol 17-Dehydrogenase; Mitochondrial RNase P Protein 2; Type 10 17b-HSD; Type II HADH; EC 1.1.1.239; EC 1.1.1.178; EC 1.1.1.159; EC 1.1.1.35; EC 1.1.1.62; EC 1.1.1.53; DUPXp11.22; HSD10MD; XH98G2; MRX17; MRX31; HCD2 Background: 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] Research Area: Neuroscience,Tags & Cell Markers,Metabolism