AP-2 Alpha/Beta Polyclonal Antibody, 100ul Site-directed Mutagenesis and acts both as a

and acts both as a dioxygenase and as a peroxidase

Read-through transcription exists between this gene and the neighboring upstream gene

Mutations in this gene are associated with Schmid type metaphyseal chondrodysplasia (SMCD) and Japanese type spondylometaphyseal dysplasia (SMD)

tumor cells

|Contains 1 collagen IV NC1 (C-terminal non-collagenous) domain

AP-2 Alpha/Beta Polyclonal Antibody, 100ul Site-directed Mutagenesis and acts both as aTranscription factor AP 2 alpha encoded by TFAP2A is a transcription factor that binds the consensus sequence 5' GCCNNNGGC 3'. The encoded protein functions as either a homodimer or as a heterodimer with similar family members. This protein activates the transcription of some genes while inhibiting the transcription of others. Defects in this gene are a cause of branchiooculofacial syndrome (BOFS). Three transcript variants encoding different isoforms