PEX16 Polyclonal Antibody, 100ul Peptide Synthesis This gene encodes a member

This gene encodes a member of the transforming acidic colied-coil protein family

suggesting a role of this cytokine in the pathogenesis of the disease

is located on chromosome on chromosome 7

The product consists of a 3D porous structure with good connectivity

Syntaxins bind synaptotagmin in a calcium-dependent fashion and interact with voltage dependent calcium and potassium channels via the C-terminal H3 domain

PEX16 Polyclonal Antibody, 100ul Peptide Synthesis This gene encodes a memberThe protein encoded by this gene is an integral peroxisomal membrane protein. An inactivating nonsense mutation localized to this gene was observed in a patient with Zellweger syndrome of the complementation group CGD CG9. Expression of this gene product morphologically and biochemically restores the formation of new peroxisomes, suggesting a role in peroxisome organization and biogenesis. Alternative splicing has been observed for this gene and two