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Phospho-NMDAR1 (Ser897)抗体

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产品名称: Phospho-NMDAR1 (Ser897)抗体
产品型号:
产品展商: XYbscience
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简单介绍

Phospho-NMDAR1 (Ser897)抗体该基因编码的蛋白质的N-甲基-D-天冬氨酸受体亚基的一个关键,谷氨酸受体通道超家族是排列成多个亚基异源蛋白复合物的配体门控离子通道成员。这些亚基在突触可塑性中起着关键作用,这种突触被认为是记忆和学习的基础。细胞特异性因子被认为控制不同亚型的表达,可能有助于亚基的功能多样性。Phospho-NMDAR1 (Ser897)抗体选择性剪接转录变体已被描述。[由RefSeq提供,月2008日]


Phospho-NMDAR1 (Ser897)抗体  的详细介绍

Phospho-NMDAR1 (Ser897)抗体特异性结合抗原:抗体本身不能直接溶解或杀伤带有特异抗原的靶细胞,通常需要补体或吞噬细胞等共同发挥效应以**病原微生物或导致病理损伤。然而,抗体可通过与病毒或**的特异性结合,直接发挥中和病毒的作用。

产品编号xy- 3903R

英文名称Phospho-NMDAR1 (Ser897)

中文名称磷酸化离子型谷氨酸受体1抗体

别    名NMDAR1 (phospho S897); p-NMDAR1 (phospho S897); NMDA-NR1; N-Methyl-d-Asprtate receptor 1; GRIN1; NMDA1; NR1; Glutamate [NMDA] receptor subunit zeta 1; Glutamate receptor ionotropic N methyl D aspartate 1; Grin 1; Grin1; N methyl D aspartate receptor channel; N-methyl-D-aspartate receptor; N-methyl-D-aspartate receptor subunit NR1; NMD-R1; NMDA 1; NMDA NR1; NMDA R1; NMDA receptor 1; NMDA1; NMDAR 1; NMDAR; NR 1; NMDZ1_HUMAN.  

说 明 书100ul  

产品类型磷酸化抗体

研究领域细胞生物  **学  神经生物学  信号转导  转录调节因子  激酶和磷酸酶  细胞膜受体  细胞类型标志物  

抗体来源Rabbit

克隆类型Polyclonal

Phospho-NMDAR1 (Ser897)抗体交叉反应 Human, Mouse, Rat, Chicken, Dog, Cow,

产品应用WB=1:500-2000 ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 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.

分 子 量103kDa

细胞定位细胞膜

性    状Lyophilized or Liquid

浓    度1mg/1ml

免 疫 原KLH conjugated Synthesised phosphopeptide derived from human NMDAR1 around the phosphorylation site of Ser897:851-938/938 <Cytoplasmic>

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.

Phospho-NMDAR1 (Ser897)抗体保存条件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.

PubMedPubMed

产品介绍background:

The protein encoded by this gene is a critical subunit of N-methyl-D-aspartate receptors, members of the glutamate receptor channel superfamily which are heteromeric protein complexes with multiple subunits arranged to form a ligand-gated ion channel. These subunits play a key role in the plasticity of synapses, which is believed to underlie memory and learning. Cell-specific factors are thought to control expression of different isoforms, possibly contributing to the functional diversity of the subunits. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jul 2008]


Function:

NMDA receptor subtype of glutamate-gated ion channels with high calcium permeability and voltage-dependent sensitivity to magnesium. Mediated by glycine. This protein plays a key role in synaptic plasticity, synaptogenesis, excitotoxicity, memory acquisition and learning. It mediates neuronal functions in glutamate neurotransmission. Is involved in the cell surface targeting of NMDA receptors.


Subunit:

Forms heteromeric channel of a zeta subunit (GRIN1), a epsilon subunit (GRIN2A, GRIN2B, GRIN2C or GRIN2D) and a third subunit (GRIN3A or GRIN3B); disulfide-linked. Found in a complex with GRIN2A or GRIN2B, GRIN3A or GRIN3B and PPP2CB. Interacts with DLG4 and MPDZ (By similarity). Interacts with LRFN1 and LRFN2 (By similarity). Interacts with MYZAP.


Subcellular Location:

Cell membrane; Multi-pass membrane protein. Cell junction, synapse, postsynaptic cell membrane. Cell junction, synapse, postsynaptic cell membrane, postsynaptic density.


Post-translational modifications:

NMDA is probably regulated by C-terminal phosphorylation of an isoform of NR1 by PKC. Dephosphorylated on Ser-897 probably by protein phosphatase 2A (PPP2CB). Its phosphorylated state is influenced by the formation of the NMDAR-PPP2CB complex and the NMDAR channel activity.


DISEASE:

Defects in GRIN1 are the cause of mental retardation autosomal dominant type 8 (MRD8) [MIM:614254]. Mental retardation is characterized by significantly below average general intellectual functioning associated with impairments in adaptative behavior and manifested during the developmental period.


Similarity:

Belongs to the glutamate-gated ion channel (TC 1.A.10.1) family. NR1/GRIN1 subfamily.


SWISS:

Q05586


Gene ID:

2902

Phospho-NMDAR1 (Ser897)抗体antibody, Ab)是由效应B细胞(效应**B细胞)分泌,机体用于抵御外来物质,如病毒,**等抗原,结构呈“Y”字型的球状蛋白质,仅仅存在于脊椎动物的血液和B**细胞膜表面。凡是能够跟抗体结合的物质,均被称作抗原,因此对于抗抗体(能够结合抗体的抗体)来说,抗体本身也是一种抗原物质。

   QQ图片20171030091318

Phospho-NMDAR1 (Ser897)抗体普通抗体重链和轻链的结构

重链结构:普通的**球蛋白具有2条重链(H链),分子量约为50kD,有μ、δ、γ、ε和α五种重链亚型,对应的**球蛋白名称分别为IgMIgGIgAIgDIgE

轻链结构:  普通**球蛋白具有2条轻链(L链),分子质量约25kDa,有κ链和λ链两种亚型,这两种轻链决定了Ig的亚型类别(IgG1IgG2IgG3IgG4)。一个天然的Ig分子两条轻链总是相同的,但在同一个体内可存在分别带有κ或λ链的抗体分子。不同种属生物体内两型轻链的比例不同,正常人血清**球蛋白κ链:λ链约为21,而在小鼠的比例为201

2.2抗体Fab段和Fc

IgG经木瓜蛋白酶酶切后裂解为2个完全相同的Fab段和1Fc,每个Fab段都为单价,可与抗原结合但不会再发生凝集反应;经胃蛋白酶酶切后裂解为1个完整F(ab)2片段和碎片化的Fc片段,F(ab)2片段为双价,可同时结合两个抗原表位。Fab段为抗原结合片段(fragment of antigen bindingFab),相当于抗体分子的两个臂,由一个完整的轻链和重链的VHCH1结构域组成。Fc段为可结晶段(fragment crystallizableFc)相当于IgCH2CH3结构域,是Ig与效应分子或者细胞相互作用的部位。Fab段包含完整的可变区,以及恒定区的CH1区域。Fc段仅指Ig恒定区CH2CH3的区域,相当于Y字结构下面那一部分。

合格 B MyB 转录因子MYB相关蛋白B抗体
合格 合格 NARG2 谷氨酸受体调节蛋白2抗体
合格 PLAG1 多型性腺瘤基因1蛋白抗体
合格 SIRT7 沉默调节样蛋白SirT7抗体
合格 合格 AARE 氧化蛋白质水解酶
合格 DAB2IP Dab2相互作用蛋白抗体
合格 DAB2 信号转导功能磷蛋白DAB2抗体
合格 HSP40 热休克蛋白家族40抗体
合格 DAL1/EPB41L3 细胞骨架4.1蛋白家族DAL1抗体
合格 FBXO31 F-box蛋白家族FBXO31抗体
合格 合格 ASAM 脂肪细胞特异性粘附分子抗体
合格 BST1 骨髓基质干细胞抗原1抗体
合格 TSLC1 细胞粘附分子1抗体
合格 CD16 FC段γ受体3/**球蛋白G Fc段受体III抗体
合格 合格 phospho-CD32B(Tyr292) 磷酸化CD32B抗体
合格 CPA1 胰羧肽酶A1抗体
合格 Protective protein/Cathepsin A 组织蛋白酶A抗体
合格 Ephrin A3 酪氨酸蛋白激酶A3受体抗体
合格 Prostaglandin dehydrogenase 1 前列腺素脱氢酶1抗体
合格 METTL11A 甲基化样蛋白11抗体(N端)
合格 IGFBP9 胰岛素样生长因子结合蛋白9抗体
合格 PRMT6 组蛋白精氨酸甲基转移酶6抗体
合格 TCF3 转录因子3抗体(螺旋环螺旋蛋白HE47)
合格 MFSD2A 促进调解蛋白家族2A抗体
合格 RASAL1 RAS蛋白样激活剂1抗体
 


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