HSD17B4 antibody

GeneTex

HSD17B4 antibody

9

WB: 0.1-0.5microg/ml. IHC-P: 0.5-1microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.

Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin

Research Use Only

Polyclonal

500 ug/ml

Unconjugated

HSD17B4

hydroxysteroid 17-beta dehydrogenase 4

DBP, MFE-2, MFP-2, MPF-2, PRLTS1, SDR8C1, peroxisomal multifunctional enzyme type 2, 17-beta-HSD 4, 17-beta-HSD IV, 17-beta-hydroxysteroid dehydrogenase 4, 17beta-estradiol dehydrogenase type IV, 3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholest-24-enoyl-CoA hydratase, D-3-hydroxyacyl-CoA dehydratase, D-bifunctional protein, peroxisomal, beta-hydroxyacyl dehydrogenase, beta-keto-reductase, epididymis secretory sperm binding protein, hydroxysteroid dehydrogenase 4, multifunctional protein 2, peroxisomal multifunctional protein 2, short chain dehydrogenase/reductase family 8C member 1

Rabbit

IgG

Peroxisomal multifunctional enzyme type 2

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]

-20°C or -80°C,2°C to 8°C

12352203