ATF-2 Polyclonal Antibody, 50ul[BT-AP00696] Deep Well Plates Mutations in this gene cause

Mutations in this gene cause Joubert syndrome

this interaction is however not essential for corepressor activity (By similarity)

The encoded protein is located in the Xq28 region and is arranged in a compact head-to-head manner with the isocitrate dehydrogenase 3 (NAD+) gamma gene and both genes are driven by a CpG-embedded bidirectional promoter

The light chain confers the protease-inhibitor function| while the heavy chains are involved in mediating protein-protein interactions with the components of the extracellular matrix

is a 2694 amino acid protein that belongs to the WD repeat Neurobeachin family

ATF-2 Polyclonal Antibody, 50ul[BT-AP00696] Deep Well Plates Mutations in this gene causeATF2 encodes a transcription factor that is a member of the leucine zipper family of DNA binding proteins. The encoded protein (activating transcription factor 2) has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions This protein binds to the cAMP responsive element (CRE), an octameric palindrome. It forms a homodimer or a heterodimer with c Jun and stimulates CRE dependent transcription. This