儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性： Monoclonal
克隆號： PT0602R
特異性： Endogenous
基因名稱： SYN1
蛋白名稱： Synapsin-1
別名： SYN1;Synapsin-1;Brain protein 4.1;Synapsin I
Organism-1： Human
基因ID-1： 6853
SwissProt-1： P17600
Organism-2： Mouse
基因ID-2： 20964
SwissProt-2： O88935
Organism-3： Rat
基因ID-3： 24949
SwissProt-3： P09951
背景： This 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. This member of the synapsin family plays a role in regulation of axonogenesis and synaptogenesis. The protein encoded serves as a substrate for several different protein kinases and phosphorylation may function in the regulation of this protein in the nerve terminal. Mutations in this gene may be associated with X-linked disorders with primary neuronal degeneration such as Rett syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008],
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性： Monoclonal
克隆號： PT0602R
特異性： Endogenous
基因名稱： SYN1
蛋白名稱： Synapsin-1
別名： SYN1;Synapsin-1;Brain protein 4.1;Synapsin I
Organism-1： Human
基因ID-1： 6853
SwissProt-1： P17600
Organism-2： Mouse
基因ID-2： 20964
SwissProt-2： O88935
Organism-3： Rat
基因ID-3： 24949
SwissProt-3： P09951
背景： This 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. This member of the synapsin family plays a role in regulation of axonogenesis and synaptogenesis. The protein encoded serves as a substrate for several different protein kinases and phosphorylation may function in the regulation of this protein in the nerve terminal. Mutations in this gene may be associated with X-linked disorders with primary neuronal degeneration such as Rett syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008],
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