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TRPM7 Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PN1443
产品名称
TRPM7 Rabbit Polyclonal Antibody
类别
常规抗体
基因名称
TRPM7 CHAK1 LTRPC7
蛋白名称
Transient receptor potential cation channel subfamily M member 7 (EC 2.7.11.1) (Channel-kinase 1) (Long transient receptor potential channel 7) (LTrpC-7) (LTrpC7)
推荐应用
WB
反应种属
Human,Rat,Mouse
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, and 0.02% New type preservative N.
Human Gene ID
54822
Human Swissprot No.
Q96QT4
Human Swissprot Link
https://www.uniprot.org/uniprotkb/Q96QT4/entry
Mouse Swissprot No.
Q923J1
Mouse Swissprot Link
http://www.uniprot.org/uniprot/Q923J1
Rat Swissprot No.
Q925B3
Rat Swissprot Link
http://www.uniprot.org/uniprot/O54941Q925B3
免疫原
Synthesized peptide derived from part region of human protein
特异性
TRPM7 Polyclonal Antibody detects endogenous levels of protein.
稀释度
WB 1:500-2000 ELISA 1:5000-20000
预测分子量
205kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
transient receptor potential cation channel subfamily M member 7(TRPM7) Homo sapiens 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. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2014],
组织表达
Colon,Liver,Placenta,
细胞定位
Membrane ; Multi-pass membrane protein .
功能
catalytic activity:ATP + a protein = ADP + a phosphoprotein.,cofactor:Binds 1 zinc ion per subunit.,disease:Defects in TRPM7 influence susceptibility to amyotrophic lateral sclerosis-parkinsonism/dementia complex type 1 [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 with unusually high incidence among the Chamorro people of the Western Pacific Islands of Guam. Both amyotrophic lateral sclerosis and parkinsonism-dementia are chronic, progressive, and uniformly fatal disorders in this population. Both diseases are known to occur in the same kindred, the same sibship, and even the same individual.,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).,PTM:Autophosphorylated.,similarity:Contains 1 alpha-type protein kinase domain.,similarity:In the C-terminal section; belongs to the protein kinase superfamily. Alpha-type protein kinase family. ALPK subfamily.,similarity:In the N-terminal section; belongs to the transient receptor family. LTrpC subfamily.,subunit:Homodimer. Interacts with PLCB1 (By similarity). Forms heterodimers with TRPM6.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

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