ACAD-10 Polyclonal Antibody, 50ul DNA/RNA Isolation & Purification May be involved in the

May be involved in the regulation of p53-dependent G2 arrest of the cell cycle

Mutations in this gene are the cause of atrioventricular septal defect

the protein mutated in Huntington disease (HD)

The Transcription factor 4 recognizes an Ephrussi-box ('E-box') binding site ('CANNTG') - a motif first identified in immunoglobulin enhancers

In normal tissues

ACAD-10 Polyclonal Antibody, 50ul DNA/RNA Isolation & Purification May be involved in theACAD10 (acyl CoA dehydrogenase family member 10) encodes a member of the acyl CoA dehydrogenase family of enzymes (ACADs), which participate in the beta oxidation of fatty acids in mitochondria. The encoded enzyme contains a hydrolase domain at the N terminal portion, a serine threonine protein kinase catlytic domain in the central region, and a conserved ACAD domain at the C terminus. Several alternatively spliced transcript variants of ACAD10 have