ARG58811

anti-17 beta HSD 4 antibody

anti-17 beta HSD 4 antibody for IHC-Formalin-fixed paraffin-embedded sections and Human

Overview

Product Description Rabbit Polyclonal antibody recognizes 17 beta HSD 4
Tested Reactivity Hu
Predict Reactivity Ms, Rat, Hm
Tested Application IHC-P
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name 17 beta HSD 4
Antigen Species Human
Immunogen Synthetic peptide corresponding to aa. 744-761 of Human 17 beta HSD 4 (NIMLSQKLQMILKDYAKL).
Conjugation Un-conjugated
Alternate Names EC 1.1.1.n12; Multifunctional protein 2; Peroxisomal multifunctional enzyme type 2; SDR8C1; EC 4.2.1.107; 17-beta-HSD 4; 3R; MFE-2; PRLTS1; 3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholest-24-enoyl-CoA hydratase; Short chain dehydrogenase/reductase family 8C member 1; 17-beta-hydroxysteroid dehydrogenase 4; DBP; MPF-2; EC 4.2.1.119; D-bifunctional protein

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-P0.5 - 1 µg/ml
Application Note IHC-P: Antigen Retrieval: By heat mediation.
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Affinity purification with immunogen.
Buffer 0.9% NaCl, 0.2% Na2HPO4, 0.05% Thimerosal, 0.05% Sodium azide and 5% BSA.
Preservative 0.05% Thimerosal and 0.05% Sodium azide
Stabilizer 5% BSA
Concentration 0.5 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 3295 Human HSD17B4

Swiss-port # P51659 Human Peroxisomal multifunctional enzyme type 2

Gene Symbol HSD17B4
Gene Full Name hydroxysteroid (17-beta) dehydrogenase 4
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]
Function Bifunctional enzyme acting on the peroxisomal beta-oxidation pathway for fatty acids. Catalyzes the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids. [UniProt]
Cellular Localization Peroxisome. [UniProt]
Calculated MW 80 kDa