SYK Monoclonal Antibody, 100ul Peptide Modification Mutations in CREBBP cause Rubinstein-Taybi

Mutations in CREBBP cause Rubinstein-Taybi syndrome (RTS)

This gene is similar to disabled-1

It is found in secretory vesicles of neurons and endocrine cells

Carboxy-terminal modifications and differences in subcellular localization allow these three proteins to respond to and act on distinct signaling molecules

SYK Monoclonal Antibody, 100ul Peptide Modification Mutations in CREBBP cause Rubinstein-TaybiPolyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. This gene is one of three similar cation transporter genes located in a cluster on chromosome 6. The encoded protein contains twelve putative transmembrane domains and is a plasma integral membrane protein. Two transcript variants