PKR2 Polyclonal Antibody, 20ul Protein Post-translational Modification MARK subfamily

MARK subfamily

and it may play a role in membrane transport and signal transduction

where it may be involved in nuclear inositol phosphate signaling processes

This gene is deleted in Williams syndrome| a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11

liver and esophagus

PKR2 Polyclonal Antibody, 20ul Protein Post-translational Modification MARK subfamilyProkineticins are secreted proteins that can promote angiogenesis and induce strong gastrointestinal smooth muscle contraction. The protein encoded by this gene is an integral membrane protein and G protein coupled receptor for prokineticins. The encoded protein is similar in sequence to GPR73, another G protein coupled receptor for prokineticins.