产品名称
							
							
								 SIX3 Rabbit Polyclonal Antibody							
						 
												
												
												
							
								蛋白名称
							
							
								Homeobox protein SIX3 (Sine oculis homeobox homolog 3)							
						 
												
												
												
												
							
								存储缓冲液
							
							
								Liquid in PBS containing 50% glycerol,  and 0.02% New type preservative N.							
						 
												
												
							
								Human Swissprot No.
							
							
								O95343							
						 
												
							
								Human Swissprot Link
							
							
								https://www.uniprot.org/uniprotkb/O95343/entry							
						 
												
							
								Mouse Swissprot No.
							
							
								Q62233							
						 
												
							
								Mouse Swissprot Link
							
							
								http://www.uniprot.org/uniprot/Q62233							
						 
												
							
								免疫原
							
							
								Synthesized peptide derived from part region of human protein							
						 
												
							
								特异性
							
							
								SIX3 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 sine oculis homeobox transcription factor family. The encoded protein plays a role in eye development. Mutations in this gene have been associated with holoprosencephaly type 2. [provided by RefSeq, Oct 2009],							
						 
												
												
												
							
								功能
							
							
								disease:Defects in SIX3 are the cause of holoprosencephaly type 2 (HPE2) [MIM:157170]. Holoprosencephaly (HPE) [MIM:236100] is the most common structural anomaly of the brain, in which the developing forebrain fails to correctly separate into right and left hemispheres. Holoprosencephaly is genetically heterogeneous and associated with several distinct facies and phenotypic variability.,function:May be involved in visual system development.,similarity:Belongs to the SIX/Sine oculis homeobox family.,similarity:Contains 1 homeobox DNA-binding domain.,							
						 
												
												
							
								纯化
							
							
								The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.