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

Individuals homozygous for a mutation in this gene are at higher risk for type 2 diabetes and have higher levels of circulating glucose and insulin levels after glucose ingestion

it has been demonstrated that the protein actually has protein disulfide isomerase activity

The protein encoded by this gene is a member of the fetuin family

MAP-9 localizes to microtubules in interphase

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