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Product Description
HSD17B4 monoclonal Antibody | MB63589 | Bioworld
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
