Synapsin I Polyclonal Antibody, 100ul[BT-AP08706] NGS Oligos Mutations in this gene caused

Mutations in this gene caused an autosomal recessive progressive myoclonic epilepsy-4 (EPM4)

which encodes a 100-kD type II transmembrane glycoprotein

1-10μl and being DNase/RNase-Free and Sterile

Centromeres are the differentiated chromosomal domains that specify the mitotic behavior of chromosomes

Synapsin I Polyclonal Antibody, 100ul[BT-AP08706] NGS Oligos Mutations in this gene causedSYN1 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. This member of the synapsin family plays a role in regulation of axonogenesis and