SYN1 Antibody Blocking Peptide(bs-3501P)-500ug

SYN1 Antibody Blocking Peptide

(bs-3501P)-500ug
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  • bs-3501P
  • 2025年10月16日
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      500ug

    产品编号bs-3501P
    英文名称SYN1 Antibody Blocking Peptide
    中文名称神经突触素1封闭多肽
    英文别名Brain protein 4.1; SYN 1; SYN 1a; SYN 1b; SYN I; SYN1; SYN1a; SYN1b; Synapsin 1; Synapsin1; SynapsinI; Synapsin-1; SYNI; SYN1_HUMAN.
    纯化方法HPLC
    研究领域

    Neuroscience > Cell Type Marker > Neuron marker > Synapse marker

    Neuroscience > Neurotransmission > Secretory Vesicles > SNAPs & SNAREs

    亚基Homodimer. Interacts with CAPON. Forms a ternary complex with NOS1. Isoform Ib interacts with PRNP.
    亚细胞定位Cell junction, synapse. Golgi apparatus.
    翻译后修饰Substrate of at least four different protein kinases. It is probable that phosphorylation plays a role in the regulation of synapsin-1 in the nerve terminal. Phosphorylated upon DNA damage, probably by ATM or ATR.
    Phosphorylation at Ser-9 dissociates synapsins from synaptic vesicles.
    相似性Belongs to the synapsin family.
    功能Neuronal phosphoprotein that coats synaptic vesicles, binds to the cytoskeleton, and is believed to function in the regulation of neurotransmitter release. The complex formed with NOS1 and CAPON proteins is necessary for specific nitric-oxid functions at a presynaptic level.
    保存条件Shipped at 4℃. Stored at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    注意事项This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    背景资料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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