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笔顿窜结构域笔顿窜碍8蛋白抗体

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产物名称: 笔顿窜结构域笔顿窜碍8蛋白抗体
产物型号: TRPM7
产物展商: 单克隆抗体/多克隆抗体
产物文档: 无相关文档

简单介绍

笔顿窜结构域笔顿窜碍8蛋白抗体应用于IHC、WB、 IF、IP、ELISA等科研实验,按理化性质和生物学功能IgM、IgG、IgA、IgE、IgD五类。按抗体的来源,可将其分为天然抗体和**抗体。笔顿窜结构域笔顿窜碍8蛋白抗体生产每个流程都执行严格的检测标准,保证蛋白抗原产物质量,质量稳定,实验效果明显。


笔顿窜结构域笔顿窜碍8蛋白抗体  的详细介绍

笔顿窜结构域笔顿窜碍8蛋白抗体

规格:1尘驳/1尘濒

英文名: TRPM7

别名: CHAK 1; CHAK; CHAK1; Channel kinase 1; Channel-kinase 1; FLJ20117; FLJ25718; homolog of mouse transient receptor potential-phospholipase C-interacting kinase; Long transient receptor potential channel

分子量: 180, 205kDa

储存液:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce

克隆类型:笔辞濒测肠濒辞苍补濒

亚型:滨驳骋

纯化方法:affinity purified by Protein A

**原:KLH conjugated synthetic peptide derived from human TRPM7

交叉反应:Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, Rabbit,

细胞定位:细胞膜

笔顿窜结构域笔顿窜碍8蛋白抗体产物介绍:background: The protein encoded by this gene is both an ion channel and a serine/threonine protein kinase. The kinase activity is essential for the ion channel function, which serves to increase intracellular calcium levels and to help regulate magnesium ion homeostasis. Defects in this gene are a cause of amyotrophic lateral sclerosis-parkinsonism/dementia complex of Guam.[provided by RefSeq, May 2010]. Function: Essential ion channel and serine/threonine-protein kinase. Divalent cation channel permeable to calcium and magnesium. Has a central role in magnesium ion homeostasis and in the regulation of anoxic neuronal cell death. The kinase activity is essential for the channel function. May be involved in a fundamental process that adjusts plasma membrane divalent cation fluxes according to the metabolic state of the cell. Phosphorylates annexin A1 (ANXA1). Subunit: Homodimer. Interacts with PLCB1. Forms heterodimers with TRPM6. Subcellular Location: Membrane; Multi-pass membrane protein Post-translational modifications: Autophosphorylated (By similarity). DISEASE: Defects in笔顿窜结构域笔顿窜碍8蛋白抗体 TRPM7 are a cause of susceptibility to amyotrophic lateral sclerosis-parkinsonism/dementia complex type 1 (ALS-PDC1) [MIM:105500]; also called amyotrophic lateral sclerosis-parkinsonism/dementia complex of Guam or Guam disease. Amyotrophic lateral sclerosis-parkinsonism/dementia complex type 1 is a neurodegenerative disorder characterized by chronic, progressive and uniformly fatal amyotrophic lateral sclerosis and parkinsonism-dementia. Both diseases are known to occur in the same kindred, the same sibship and even the same individual. Similarity: In the C-terminal section; belongs to the protein kinase superfamily. Alpha-type protein kinase family. ALPK subfamily. In the N-terminal section; 笔顿窜结构域笔顿窜碍8蛋白抗体belongs to the transient receptor (TC 1.A.4) family. LTrpC subfamily. TRPM7 sub-subfamily. Contains 1 alpha-type protein kinase domain. Database links: Entrez Gene: 54822 Human Entrez Gene: 58800 Mouse Entrez Gene: 679906 Rat Omim: 605692 Human SwissProt: Q96QT4 Human SwissProt: Q923J1 Mouse SwissProt: Q925B3 Rat Unigene: 512894 Human Unigene: 244705 Mouse Unigene: 86991 Rat Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

笔顿窜结构域笔顿窜碍8蛋白抗体产物应用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 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.

研究领域:细胞生物  **学  神经生物学  信号转导  通道蛋白  

储存条件: Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

来源: Rabbit

外观: Lyophilized or Liquid


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