HSD17B4 monoclonal Antibody | MB63589

HSD17B4 monoclonal Antibody | MB63589 | Gentaur UK, US & Europe Distribution

Host: Mouse

Reactivity: Human, Mouse, Rat

Application: IF, IHC, WB

Application Range: WB 1:4000, IHC 1:150, IF 1:100

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. [provided by RefSeq, Jul 2008]

Storage & Stability: PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.

Specificity: hydroxysteroid (17-beta) dehydrogenase 4

Molecular Weight: 79.5 kDa (Predicted)

Note: For research use only, not for use in diagnostic procedure.

Alternative Names: DBP; MFE-2; MPF-2; PRLTS1; SDR8C1

Immunogen: Full length human recombinant protein of human HSD17B4 (NP_000405) produced in HEK293T cell.

Conjugate: Unconjugated

Modification: Unmodification

Purification & Purity: Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)

Pathway: N/A