产品名称
							
							
								 IRK13 Rabbit Polyclonal Antibody							
						 
												
												
												
							
								蛋白名称
							
							
								Inward rectifier potassium channel 13 (Inward rectifier K(+) channel Kir7.1) (Potassium channel, inwardly rectifying subfamily J member 13)							
						 
												
												
												
												
							
								存储缓冲液
							
							
								Liquid in PBS containing 50% glycerol,  and 0.02% New type preservative N.							
						 
												
												
							
								Human Swissprot No.
							
							
								O60928							
						 
												
							
								Human Swissprot Link
							
							
								https://www.uniprot.org/uniprotkb/O60928/entry							
						 
												
							
								Mouse Swissprot No.
							
							
								P86046							
						 
												
							
								Mouse Swissprot Link
							
							
								http://www.uniprot.org/uniprot/P86046							
						 
												
												
							
								Rat Swissprot Link
							
							
								http://www.uniprot.org/uniprot/O54941O70617							
						 
												
							
								免疫原
							
							
								Synthesized peptide derived from part region of human protein							
						 
												
							
								特异性
							
							
								IRK13 Polyclonal Antibody detects endogenous levels of protein.							
						 
												
							
								稀释度
							
							
								WB 1:500-2000 ELISA 1:5000-20000							
						 
												
												
												
							
								宿主
							
							
								Polyclonal, Rabbit,IgG							
						 
												
							
								背景介绍
							
							
								 This gene encodes a member of the inwardly rectifying potassium channel family of proteins. Members of this family form ion channel pores that allow potassium ions to pass into a cell. The encoded protein belongs to a subfamily of low signal channel conductance proteins that have a low dependence on potassium concentration. Mutations in this gene are associated with snowflake vitreoretinal degeneration. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Feb 2010],							
						 
												
							
								组织表达
							
							
								Predominantly expressed in small intestine. Expression is also detected in stomach, kidney, and all central nervous system regions tested with the exception of spinal cord.							
						 
												
							
								细胞定位
							
							
								Membrane; Multi-pass membrane protein.							
						 
												
							
								功能
							
							
								disease:Defects in KCNJ13 are the cause of snowflake vitreoretinal degeneration (SVD) [MIM:193230]. SVD is a developmental and progressive hereditary eye disorder that affects multiple tissues within the eye. Diagnostic features of SVD include fibrillar degeneration of the vitreous humor, early-onset cataract, minute crystalline deposits in the neurosensory retina, and retinal detachment.,function:Inward rectifier potassium channels are characterized by a greater tendency to allow potassium to flow into the cell rather than out of it. Their voltage dependence is regulated by the concentration of extracellular potassium; as external potassium is raised, the voltage range of the channel opening shifts to more positive voltages. The inward rectification is mainly due to the blockage of outward current by internal magnesium. KCNJ13 has a very low single channel conductance, low sensitivity to block by external barium and cesium, and no dependence of its inward rectification properties on the internal blocking particle magnesium.,similarity:Belongs to the inward rectifier-type potassium channel family.,tissue specificity:Predominantly expressed in small intestine. Expression is also detected in stomach, kidney, and all central nervous system regions tested with the exception of spinal cord.,							
						 
												
												
							
								纯化
							
							
								The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.