Anti-SYN1/Synapsin 1神经突触素1抗体

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bioss
国产
2022-03-25 11:45

上海恪敏生物科技有限公司

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上海恪敏生物科技有限公司
王羽
18021003406
1914109725@qq.com
产品属性
保存条件-20℃
是否单克隆2
抗体英文名Anti-SYN1/Synapsin 1
抗原来源详询
保质期1年
供应商上海科敏
应用范围WB,IHC-P,IHC-F,ICC,IF, Elisa
适应物种hu, rat, mo, pig
宿主
规格100ug
产品说明
本公司提供科研SYN1/Synapsin 1神经突触素1抗体,抗体质量可靠,订购SYN1/Synapsin 1神经突触素1抗体请联系在线客服或者销售人员。
抗体参数如下>>>>
中文名称:神经突触素1抗体
英文名称:Anti-SYN1/Synapsin 1
货号:bs-3501R
抗体来源:兔
克隆类型:多克隆
蛋白分子量:predicted molecular weight: 85kDa
纯化方法:affinity purified by Protein A
交叉反应:hu, rat, mo, pig
测试应用:ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500
(石蜡切片需做抗原修复)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
产品背景介绍:Synapsin I is a member of the synapsin family. Synapsins are 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 serves as a substrate for several different protein kinases and phosphorylation may function in the regulation of this protein in the nerve terminal. Mutations of the Synapsin I gene may be associated with X linked disorders with primary neuronal degeneration such as Rett syndrome.Function : 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.Subcellular Location : Cell junction > synapse. Golgi apparatus.Post-translational modifications : 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.DISEASE : Defects in SYN1 are a cause of epilepsy X-linked with variable learning disabilities and behavior disorders [MIM:300491]. XELBD is characterized by variable combinations of epilepsy, learning difficulties, macrocephaly, and aggressive behavior.Similarity : Belongs to the synapsin family.