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LIMK-1/2 (PTR2545) Mouse mAb

-YM4686

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主要信息
Target

LIMK-1/2

Host Species

Mouse

Reactivity

Human, Mouse, Rat,

Applications

WB, IF, ELISA

MW

68kD,72kD (Observed)

Conjugate/Modification

Unmodified

货号: YM4686
规格
价格
货期
数量
200μL
¥3,780.00
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0

100μL
¥2,300.00
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0

40μL
¥960.00
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0

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详细信息
推荐稀释比
WB 1:500-2000; IF 1:100-500; ELISA 1:1000-5000
组成
PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
特异性
This antibody detects endogenous levels of LIMK-1/2 protein.
纯化工艺
Protein G
储存
-15°C to -25°C/1 year(Do not lower than -25°C)
实测条带
68kD,72kD
修饰
Unmodified
克隆性
Monoclonal
克隆号
PTR2545
同种型
IgG1,Lambda
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抗原&靶点信息
免疫原:
Synthesized peptide derived from human LIMK-1/2 AA range: 500-600
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特异性:
This antibody detects endogenous levels of LIMK-1/2 protein.
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基因名称:
LIMK1 LIMK
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蛋白名称:
LIM domain kinase 1 (LIMK-1) (EC 2.7.11.1)
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别名:
LIM domain kinase 1 ;
LIMK-1 ;
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数据库链接:
Organism 基因 ID SwissProt
Human 3984;3985; P53667;P53671;
Rat P53669;
背景:
LIM domain kinase 1(LIMK1) Homo sapiens There are approximately 40 known eukaryotic LIM proteins, so named for the LIM domains they contain. LIM domains are highly conserved cysteine-rich structures containing 2 zinc fingers. Although zinc fingers usually function by binding to DNA or RNA, the LIM motif probably mediates protein-protein interactions. LIM kinase-1 and LIM kinase-2 belong to a small subfamily with a unique combination of 2 N-terminal LIM motifs and a C-terminal protein kinase domain. LIMK1 is a serine/threonine kinase that regulates actin polymerization via phosphorylation and inactivation of the actin binding factor cofilin. This protein is ubiquitously expressed during development and plays a role in many cellular processes associated with cytoskeletal structure. This protein also stimulates axon growth and may play a role in brain development. LIMK1 hemizygosity is implicated in the impaired visuospatial constructive cog
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功能:
Catalytic activity:ATP + a protein = ADP + a phosphoprotein.,Disease:Haploinsufficiency of LIMK1 may be the cause of certain cardiovascular and musculo-skeletal abnormalities observed in Williams-Beuren syndrome (WBS), a rare developmental disorder. It is a contiguous gene deletion syndrome involving genes from chromosome band 7q11.23.,Function:Protein kinase which regulates actin filament dynamics. Phosphorylates and inactivates the actin binding/depolymerizing factor cofilin, thereby stabilizing the actin cytoskeleton. Isoform 3 has a dominant negative effect on actin cytoskeletal changes. May be involved in brain development.,PTM:Autophosphorylated.,PTM:Phosphorylated on serine and/or threonine residues by ROCK1. May be dephosphorylated and inactivated by SSH1.,similarity:Belongs to the protein kinase superfamily. TKL Ser/Thr protein kinase family.,similarity:Contains 1 PDZ (DHR) domain.,similarity:Contains 1 protein kinase domain.,similarity:Contains 2 LIM zinc-binding domains.,subunit:Self-associates. The LIM domain interacts with the cytoplasmic domain of NRG1. Binds ROCK1. Interacts with SSH1. Interacts with NISCH.,tissue specificity:Highest expression in both adult and fetal nervous system. Detected ubiquitously throughout the different regions of adult brain, with highest levels in the cerebral cortex. Expressed to a lesser extent in heart and skeletal muscle.,
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组织表达:
Highest expression in both adult and fetal nervous system. Detected ubiquitously throughout the different regions of adult brain, with highest levels in the cerebral cortex. Expressed to a lesser extent in heart and skeletal muscle.
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研究领域:
>>Axon guidance ;
>>Fc gamma R-mediated phagocytosis ;
>>Regulation of actin cytoskeleton ;
>>Yersinia infection ;
>>Human immunodeficiency virus 1 infection
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货号: YM4686
规格
价格
货期
数量
200μL
¥3,780.00
现货

0

100μL
¥2,300.00
现货

0

40μL
¥960.00
现货

0

加入购物车

已收藏

收藏

定制服务咨询

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