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磷酸化神經(jīng)突觸前膜胞內(nèi)蛋白抗體品牌 英文名稱  Anti-phospho-STXBP1(Ser515)

中文名稱  磷酸化神經(jīng)突觸前膜胞內(nèi)蛋白抗體品牌 

別    名 Stxbp1(phospho S515); FLJ37475; hUNC 18; hUNC18; Munc 18 1; Munc 18; Munc 18a; Munc18 1; Munc18a; N Sec1; N-Sec1; Neuronal SEC1; NSec1; p67; Protein unc-18 homolog 1; Protein unc-18 homolog A; Rb sec1; RBSEC1; STX BP1; STXB1_HUMAN; STXBP 1; STXBP1; Syntaxin binding protein 1; Syntaxin-binding protein 1; Unc 18 1; UNC 18; Unc 18 homolog; Unc 18A; Unc-18A; Unc18 1; UNC18; Unc18 homolog; Unc18-1; Unc18A.

產(chǎn)品屬性：

濃    度  1mg/1ml

規(guī) 格  0.1ml/100μg

抗體來源  Rabbit

克隆類型   polyclonal

交叉反應(yīng)   Human, Mouse, Rat

產(chǎn)品類型   一抗 磷酸化抗體  

研究領(lǐng)域     細(xì)胞生物 免疫學(xué) 神經(jīng)生物學(xué) 結(jié)合蛋白

蛋白分子量  predicted molecular weight: 68kDa 

性    狀   Lyophilized or Liquid

免 疫 原  KLH conjugated Synthesised phosphopeptide derived from human STXBP1 around the phosphorylation site of Ser515

亞    型  IgG

純化方法   affinity purified by Protein A

儲(chǔ) 存 液   0.01M PBS, pH 7.4 with 10 mg/ml BSA and 0.1% Sodium azide

磷酸化神經(jīng)突觸前膜胞內(nèi)蛋白抗體品牌 產(chǎn)品應(yīng)用   WB=1:100-500 ELISA=1:500-1000 IP=1:20-100 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500

（石蠟切片需做抗原修復(fù)） 

 not yet tested in other applications.

 optimal dilutions/concentrations should be determined by the end user.  

保存條件  Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C. 

Important Note  This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. 

產(chǎn)品介紹 Munc18 may participate in the regulation of synaptic vesicle docking and fusion, possibly through interaction with GTP binding proteins. It is essential for neurotransmission and binds syntaxin, a component of the synaptic vesicle fusion machinery probably in a 1:1 ratio. Munc18 can interact with syntaxins 1, 2, and 3 but not syntaxin 4. It may play a role in determining the specificity of intracellular fusion reactions. Mutations in Munc18 can result in accumulations of acetylcholine and paralytic phenotype suggestive of a neurotransmitter release defect. Two Munc18 isoforms have recently been identified. Munc18-1 has been shown to be primarily expressed in brain, while Munc18-2 is expressed in most tissues.

Function : May participate in the regulation of synaptic vesicle docking and fusion, possibly through interaction with GTP-binding proteins. Essential for neurotransmission and binds syntaxin, a component of the synaptic vesicle fusion machinery probably in a 1:1 ratio. Can interact with syntaxins 1, 2, and 3 but not syntaxin 4. May play a role in determining the specificity of intracellular fusion reactions.

Subunit : Binds SYTL4 (By similarity). Interacts with STX1A.

Subcellular Location : Cytoplasm. Membrane; Peripheral membrane protein.

Tissue Specificity : Brain and spinal cord. Highly enriched in axons.

DISEASE : Defects in STXBP1 are the cause of epileptic encephalopathy early infantile type 4 (EIEE4) [MIM:612164]. Affected individuals have neonatal or infantile onset of seizures, suppression-burst pattern on EEG, profound mental retardation, and MRI evidence of hypomyelination.

Similarity : Belongs to the STXBP/unc-18/SEC1 family.

Database links : UniProtKB/Swiss-Prot: P61764.1

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