HSD17B4 anticorps

N° du produit ABIN5647728

Détail du produit anti-HSD17B4 anticorps

Antigène: HSD17B4 (Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp HSD17B4 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Purification: Antigen affinity purified

Immunogène: Amino acids D510-L736 from the human protein were used as the immunogen for the HSD17B4 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the HSD17B4 antibody should be determined by the researcher.\. WB: 0.5-1 μg/mL,IHC (FFPE): 1-2 μg/mL

Restrictions: For Research Use only

Stockage

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: -20 °C

Stockage commentaire: After reconstitution, the HSD17B4 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.

Détails sur HSD17B4

Antigène: HSD17B4 (Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4))

Autre désignation: 17-beta-Hydroxysteroid dehydrogenase 4 (HSD17B4) (HSD17B4 Produits)

Synonymes: anticorps zgc:55545, anticorps zgc:77300, anticorps CG3415, anticorps DmMFE-2, anticorps Dmel\\CG3415, anticorps MFE-2, anticorps DBP, anticorps MPF-2, anticorps PRLTS1, anticorps SDR8C1, anticorps 17-beta-HSD, anticorps 17[b]-HSD, anticorps 4, anticorps MFP2, anticorps Mfp-2, anticorps perMFE-2, anticorps hydroxysteroid (17-beta) dehydrogenase 4, anticorps hydroxysteroid 17-beta dehydrogenase 4, anticorps peroxisomal Multifunctional enzyme type 2, anticorps hsd17b4, anticorps HSD17B4, anticorps Mfe2, anticorps Hsd17b4

Sujet: Peroxisomal multifunctional enzyme type 2 is a protein that in humans is encoded by the HSD17B4 gene. 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.

UniProt: P51659

Pathways: Monocarboxylic Acid Catabolic Process