产品名称
							
							
								 HXA11 Rabbit Polyclonal Antibody							
						 
												
												
												
							
								蛋白名称
							
							
								Homeobox protein Hox-A11 (Homeobox protein Hox-1I)							
						 
												
												
												
												
							
								存储缓冲液
							
							
								Liquid in PBS containing 50% glycerol,  and 0.02% New type preservative N.							
						 
												
												
							
								Human Swissprot No.
							
							
								P31270							
						 
												
							
								Human Swissprot Link
							
							
								https://www.uniprot.org/uniprotkb/P31270/entry							
						 
												
							
								Mouse Swissprot No.
							
							
								P31311							
						 
												
							
								Mouse Swissprot Link
							
							
								http://www.uniprot.org/uniprot/P31311							
						 
												
							
								免疫原
							
							
								Synthesized peptide derived from part region of human protein							
						 
												
							
								特异性
							
							
								HXA11 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
							
							
								 In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. This gene is involved in the regulation of uterine development and is required for female fertility. Mutations in this gene can cause radio-ulnar synostosis with amegakaryocytic thrombocytopenia. [provided by RefSeq, Jul 2008],							
						 
												
												
												
							
								功能
							
							
								disease:Defects in HOXA11 are the cause of radioulnar synostosis with amegakaryocytic thrombocytopenia [MIM:605432]. The syndrome consists of an unusual association of bone marrow failure and skeletal defects. Patients have the same skeletal defects, the proximal fusion of the radius and ulna, resulting in extremely limited pronation and supination of the forearm. Some patients have also symptomatic thrombocytopenia, with bruising and bleeding problems since birth, necessitating correction by bone marrow or umbilical-cord stem-cell transplantation.,function:Sequence-specific transcription factor which is part of a developmental regulatory system that provides cells with specific positional identities on the anterior-posterior axis.,similarity:Belongs to the Abd-B 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.