ACSS1 (Acetyl-K642) Polyclonal Antibody, 100ul Cell Culture Plates This gene encodes a member

This gene encodes a member of a family of proteins that function as negative regulators of Wnt receptor signaling through interaction with Dishevelled family members

and functions as a critical regulator of all-trans retinoic acid levels by the specific inactivation of all-trans retinoic acid to hydroxylated forms

This gene is deleted in Williams syndrome| a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11

and inhibit their ability to transactivate by preventing their binding to their DNA response elements

ACSS1 (Acetyl-K642) Polyclonal Antibody, 100ul Cell Culture Plates This gene encodes a memberThis gene encodes a mitochondrial acetyl CoA synthetase enzyme. A similar protein in mice plays an important role in the tricarboxylic acid cycle by catalyzing the conversion of acetate to acetyl CoA. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.