OCRL Polyclonal Antibody, 50ul Digital Burette Deficiency of this enzyme results

Deficiency of this enzyme results in the accumulation of branched fatty acids and bile acid intermediates| and may lead to Zellweger syndrome| severe mental retardation| and death in children

subunit:Homotetramer of alpha or beta subunits

The immunoproteasome contains an alternate regulator

Positively regulates vesicle fusion by maintaining the readily releasable pool of secretory vesicles (By similarity)

OCRL Polyclonal Antibody, 50ul Digital Burette Deficiency of this enzyme resultsOCRL encodes an inositol polyphosphate 5 phosphatase. OCRL, inositol polyphosphate 5 phosphatase is involved in regulating membrane trafficking and is located in numerous subcellular locations including the trans Golgi network, clathrin coated vesicles and, endosomes and the plasma membrane. OCRL, inositol polyphosphate 5 phosphatase may also play a role in primary cilium formation. Mutations in OCRL cause oculocerebrorenal syndrome of Lowe and also