HSD17B4 Antikörper

Produktnummer ABIN5647728

Produktdetails anti-HSD17B4 Antikörper

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

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser HSD17B4 Antikörper ist unkonjugiert

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

Aufreinigung: Antigen affinity purified

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

Isotyp: IgG

Anwendungsinformationen

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

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

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

Lagerung: -20 °C

Informationen zur Lagerung: 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.

Details zu HSD17B4

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

Andere Bezeichnung: 17-beta-Hydroxysteroid dehydrogenase 4 (HSD17B4) (HSD17B4 Produkte)

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

Hintergrund: 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