突触小泡蛋白P38重组兔单克隆抗体-抗体-抗体-生物在线
上海雅吉生物科技有限公司
突触小泡蛋白P38重组兔单克隆抗体

突触小泡蛋白P38重组兔单克隆抗体

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产品名称: 突触小泡蛋白P38重组兔单克隆抗体

英文名称: Synaptophysin

产品编号: YJ-52951

产品价格: null

产品产地: 上海

品牌商标: 雅吉

更新时间: null

使用范围: WB, IF, ICC

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 中文名称 突触小泡蛋白P38重组兔单克隆抗体 
别    名 Major synaptic vesicle protein P38; MRXSYP; Syn p38; Synaptophysin; SYP; SYPH; SYPH_HUMAN; SypI.   
研究领域 细胞生物  神经生物学   
抗体来源 Rabbit 
克隆类型 Monoclonal 
克 隆 号 2B1 
交叉反应 (predicted: Human, Mouse, Rat, ) 
产品应用 WB=1:1000-5000 IHC-P=1:50-200 IHC-F=1:50-200 ICC=1:50-200 IF=1:50-200 (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. 
分 子 量 34kDa 
细胞定位 细胞浆  
性    状 Liquid 
浓    度 1mg/ml 
免 疫 原 KLH conjugated synthetic peptide derived from human Synaptophysin:  
亚    型 IgG 
纯化方法 affinity purified by Protein A 
储 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. 
保存条件 Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. 
PubMed PubMed 
产品介绍 This gene encodes an integral membrane protein of small synaptic vesicles in brain and endocrine cells. The protein also binds cholesterol and is thought to direct targeting of vesicle-associated membrane protein 2 (synaptobrevin) to intracellular compartments. Mutations in this gene are associated with X-linked mental retardation (XLMR). [provided by RefSeq, Aug 2011]
 
Function:
Possibly involved in structural functions as organizing other membrane components or in targeting the vesicles to the plasma membrane. Involved in the regulation of short-term and long-term synaptic plasticity.
 
Subcellular Location:
Cytoplasmic vesicle > secretory vesicle > synaptic vesicle membrane. Cell junction > synapse > synaptosome.
 
Tissue Specificity:
Characteristic of a type of small (30-80 nm) neurosecretory vesicles, including presynaptic vesicles, but also vesicles of various neuroendocrine cells of both neuronal and epithelial phenotype.
 
Post-translational modifications:
Ubiquitinated; mediated by SIAH1 or SIAH2 and leading to its subsequent proteasomal degradation.
 
DISEASE:
Defects in SYP are the cause of mental retardation X-linked SYP-related (MRXSYP) [MIM:300802]. Mental retardation is characterized by significantly below average general intellectu