KD-Validated HSD17B4 Mouse Monoclonal Antibody

Description

EnkiLife offers the KD-Validated HSD17B4 Mouse Monoclonal Antibody. This antibody reacts with Human,M 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 1:400-1:2,000; FC 1:200-1:2,000; ICC 1:100-1:1,000 Alternative Names of Immunogen:HSD17B4; Hydroxysteroid 17-Beta Dehydrogenase 4; SDR8C1; MFE-2; DBP; 17-Beta-Hydroxysteroid Dehydrogenase 4; 3-Alpha,7-Alpha,12-Alpha-Trihydroxy-5-Beta-Cholest-24-Enoyl-CoA Hydratase; Short Chain Dehydrogenase/Reductase Family 8C Member 1; Peroxisomal Multifunctional Enzyme Type 2; 17beta-Estradiol Dehydrogenase Type IV; Peroxisomal Multifunctional Protein 2; D-Bifunctional Protein, Peroxisomal; D-3-Hydroxyacyl-CoA Dehydratase; Beta-Hydroxyacyl Dehydrogenase; Multifunctional Protein 2; Beta-Keto-Reductase; 17-Beta-HSD IV; 17-Beta-HSD 4; MFP-2; Short Chain Dehydrogenase/Reductase Family 8C, Member 1; Epididymis Secretory Sperm Binding Protein; Hydroxysteroid (17-Beta) Dehydrogenase 4; Hydroxysteroid Dehydrogenase 4; D-Bifunctional Protein; EDH17B4; PRLTS1; MPF-2 Background: The protein encoded by this gene is a bifunctional enzyme that is involved in the peroxisomal beta-oxidation pathway for fatty acids. It also acts as a catalyst for the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids. Defects in this gene that affect the peroxisomal fatty acid beta-oxidation activity are a cause of D-bifunctional protein deficiency (DBPD). An apparent pseudogene of this gene is present on chromosome 8. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2014] Research Area: Signal Transduction,Cancer,Cardiovascular,Metabolism