SYN3 Polyclonal Antibody, 50ul High Speed Micro-Centrifuges Mutations in this gene are

Mutations in this gene are associated with pyruvate dehydrogenase E1-alpha deficiency and X-linked Leigh syndrome

acting on carbon-nitrogen (but not peptide) bonds

telomere maintenance

tissue specificity:Predominantly expressed in thymus

The encoded protein interacts with IRS1 protein| suggesting a role in regulating insulin sensitivity

SYN3 Polyclonal Antibody, 50ul High Speed Micro-Centrifuges Mutations in this gene areThis gene is a member of the synapsin gene family. Synapsins encode neuronal phosphoproteins which associate with the cytoplasmic surface of synaptic vesicles. Family members are characterized by common protein domains, and they are implicated in synaptogenesis and the modulation of neurotransmitter release, suggesting a potential role in several neuropsychiatric diseases. The protein encoded by this gene shares the synapsin family domain model, with