HSD17B4,ID (HSD17B4,EDH17B4,Peroxisomal multifunctional enzyme type 2,17-beta-hydroxysteroid dehydrogenase 4,D-bifunctional protein,Multifunctional protein 2,(3R)-hydroxyacyl-CoA dehydrogenase,Enoyl-CoA hydratase 2,3-alp

Antibodies / Antibodies-Enzymes, Dehydrogenase

-20°C

Supplied as a liquid in PBS, pH 7.2, 0.09% sodium azide.

HSD17B4 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 340-370 amino acids from the Central region of human HSD17B4.

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].

Applications:
Suitable for use in Western Blot, Immunohistochemistry, ELISA

Recommended Dilution:
ELISA: 1:1, 000
Western Blot: 1:100-500
Immunohistochemistry: 1:10-50

Storage and Stability:
May be stored at 4°C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20°C. Aliquots are stable for 12 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.