GDF-6 Polyclonal Antibody, 100ul In vitro Transcription Defects in EP300 are a

Defects in EP300 are a cause of Rubinstein-Taybi syndrome and may also play a role in epithelial cancer

Adenosine has widespread effects on the cardiovascular

Component of the SCF(BTRC) complex containing BTRC

A related pseudogene is located on the X chromosome

known as SL1

GDF-6 Polyclonal Antibody, 100ul In vitro Transcription Defects in EP300 are aGDF6 encodes a member of the bone morphogenetic protein (BMP) family and the TGF beta superfamily of secreted signaling molecules. It is required for normal formation of some bones and joints in the limbs, skull, and axial skeleton. Mutations in this gene result in colobomata, which are congenital abnormalities in ocular development, and in Klippel Feil syndrome (KFS), which is a congenital disorder of spinal segmentation.