储存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性： Monoclonal
克隆号： PT0625R
特异性： Endogenous
基因名称： VCL
蛋白名称： Vinculin
别名： VCL;Vinculin;Metavinculin
Organism-1： Human
基因ID-1： 7414
SwissProt-1： P18206
Organism-2： Mouse
基因ID-2： 22330
SwissProt-2： Q64727
Organism-3： Rat
基因ID-3： 305679
SwissProt-3： P85972
背景： Vinculin is a cytoskeletal protein associated with cell-cell and cell-matrix junctions, where it is thought to function as one of several interacting proteins involved in anchoring F-actin to the membrane. Defects in VCL are the cause of cardiomyopathy dilated type 1W. Dilated cardiomyopathy is a disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Multiple alternatively spliced transcript variants have been found for this gene, but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008],
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性： Monoclonal
克隆号： PT0625R
特异性： Endogenous
基因名称： VCL
蛋白名称： Vinculin
别名： VCL;Vinculin;Metavinculin
Organism-1： Human
基因ID-1： 7414
SwissProt-1： P18206
Organism-2： Mouse
基因ID-2： 22330
SwissProt-2： Q64727
Organism-3： Rat
基因ID-3： 305679
SwissProt-3： P85972
背景： Vinculin is a cytoskeletal protein associated with cell-cell and cell-matrix junctions, where it is thought to function as one of several interacting proteins involved in anchoring F-actin to the membrane. Defects in VCL are the cause of cardiomyopathy dilated type 1W. Dilated cardiomyopathy is a disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Multiple alternatively spliced transcript variants have been found for this gene, but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008],
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