Product Name: HSD17B4 Antibody
Species Reactivity: Human
Tested Applications: IHC-P, WB
Applications: For WB starting dilution is: 1:1000For IHC-P starting dilution is: 1:10~50
User Note: Optimal dilutions for each application to be determined by the researcher.
Predicted Molecular Weight: 80 kDa
Immunogen: This HSD17B4 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 341-370 amino acids from the Central region of human HSD17B4.
Host Species: Rabbit
Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.
Physical State: Liquid
CAS NO.: 99291-25-5
Product: SZL P1-41
Buffer: Supplied in PBS with 0.09% (W/V) sodium azide.
Concentration: 0.25 mg/ml
Storage Conditions: Store at 4˚C for three months and -20˚C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
Clonality: Polyclonal
Conjugate: Unconjugated
Alternate Names: Peroxisomal multifunctional enzyme type 2, MFE-2, 17-beta-hydroxysteroid dehydrogenase 4, 17-beta-HSD 4, D-bifunctional protein, DBP, Multifunctional protein 2, MPF-2, (3R)-hydroxyacyl-CoA dehydrogenase, 111n12, Enoyl-CoA hydratase 2, 3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholest-24-enoyl-CoA hydratase, HSD17B4, EDH17B4
Accession NO.: P51659
Protein Ino: 1706396
Official Symbol: HSD17B4
Geneid: 3295
Background: The protein encoded by this gene is a bifunctional enzymethat is involved in the peroxisomal beta-oxidation pathway forfatty acids. It also acts as a catalyst for the formation of3-ketoacyl-CoA intermediates from both straight-chain and2-methyl-branched-chain fatty acids. Defects in this gene thataffect the peroxisomal fatty acid beta-oxidation activity are acause of D-bifunctional protein deficiency (DBPD). An apparentpseudogene of this gene is present on chromosome 8. [provided byRefSeq].
PubMed ID:http://aac.asm.org/content/24/1/95.abstract
