货号 | 5355S |
反应种属 | Mouse/Rat |
来源宿主 | Rabbit |
应用 | W/IP |
目标/特异性 | Phospho-NMDAR2B (Ser1284) Antibody recognizes endogenous levels of NMDAR2B protein only when phosphorylated at Ser1284. |
使用方法 | WB(1:1000) IP (1:50) |
供应商 | CST |
背景 | N-methyl-D-aspartate receptor (NMDAR) forms a heterodimer of at least one NR1 and one NR2A-D subunit. Multiple receptor isoforms with distinct brain distributions and functional properties arise by selective splicing of the NR1 transcripts and differential expression of the NR2 subunits. NR1 subunits bind the co-agonist glycine and NR2 subunits bind the neurotransmitter glutamate. Activation of the NMDA receptor or opening of the ion channel allows flow of Na+ and Ca2+ ions into the cell, and K+ out of the cell (1). Each subunit has a cytoplasmic domain that can be directly modified by the protein kinase/phosphatase (2). PKC can phosphorylate the NR1 subunit (NMDAR1) of the receptor at Ser890/Ser896, and PKA can phosphorylate NR1 at Ser897 (3). The phosphorylation of NR1 by PKC decreases its affinity for calmodulin, thus preventing the inhibitory effect of calmodulin on NMDAR (4). The phosphorylation of NR1 by PKA probably counteracts the inhibitory effect of calcineurin on the receptor (5). NMDAR mediates long-term potentiation and slow postsynaptic excitation, which play central roles in learning, neurodevelopment, and neuroplasticity (6).Ephrin-B2 binding to its receptor EphB leads to the activation of Src family tyrosine kinases, which phosphorylate NMDAR2B at Tyr1252, Tyr1336, and Tyr1472. In turn, phosphorylated NMDAR2B enhances the ability of the functional NMDA receptor to regulate Ca2+ influx in response to glutamate (7). Phosphorylation of NMDAR2B at Ser1284 was identified at Cell Signaling Technology (CST) using PhosphoScan®, an MS/MS platform for phosphorylation site discovery. Phosphorylation of NMDAR2B at Ser1284 was observed in extracts isolated from embryo and adult mouse brain. For additional information please visit PhosphoSitePlus®, a CST modification site knowledgebase, at www.phosphosite.org. |
存放说明 | -20C |
计算分子量 | 190 |
Western blot analysis of extracts from rat brain using Phospho-NMDAR2B (Ser1284) Antibody. The phospho-specificity of the antibody was verified by blocking with a phospho or non-phosphopeptide. Western blot分析大鼠大脑提取物,使用的抗体是Phospho-NMDAR2B (Ser1284) Antibody 兔多抗。抗体的磷酸化特异性由磷酸化或非磷酸化肽段封闭实验进行验证。 |