EHHADH polyclonal, anti-human, mouse

Background:
The protein encoded by this gene is a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of the encoded protein contains enoyl-CoA hydratase activity while the C-terminal region contains 3-hydroxyacyl-CoA dehydrogenase activity. Defects in this gene are a cause of peroxisomal disorders such as Zellweger syndrome. Two transcript variants encoding different isoforms have been found for this gene.

Synonyms: LBP, ECHD, LBFP, PBFE, L-PBE

Cellular Location: Cytoplasm

Immunogen:
Recombinant protein of human EHHADH

Gene Symbol: EHHADH

Gene ID: 1962

Swiss prot: Q08426

Calculated MW: 79kDa

Recommended dilution:
WB 1:200-1000, IHC 1:50-200,

Purity:
Affinity purification

Storage Buffer:
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.

Storage:
Store at -20℃. Avoid freeze / thaw cycles.