本公司经销HOXA6/HOX1B,同源盒基因HOXA6蛋白抗体,克隆类型为polyclonal,宿主来源是Rabbit,HOXA6/HOX1B同源盒基因HOXA6蛋白抗体可应用于WB、elisa、IP、IF、IHC等实验,欢迎垂询订购!
本公司经销HOXA6/HOX1B,同源盒基因HOXA6蛋白抗体,克隆类型为polyclonal,宿主来源是Rabbit,HOXA6/HOX1B同源盒基因HOXA6蛋白抗体可应用于WB、elisa、IP、IF、IHC等实验,欢迎垂询订购!
货号:BY-11294R
英文名称:Anti-HOXA6/HOX1B
中文名称:同源盒基因HOXA6蛋白抗体
其他名称:名Homeo box 1B;Homeo box A6;Homeobox 1B;Homeobox A6;Homeobox protein Hox A6;Homeobox protein Hox-1B;Homeobox protein Hox-A6 antibodyHomeobox protein HoxA6;HOX 1;Hox 1B;HOX1;HOX1.2;Hox1B;HOXA6;HX A6;HXA6;HXA6_HUMAN.
抗体来源:Rabbit
克隆类型:polyclonal
蛋白分子量:predicted molecular weight: 34kDa
纯化方法:affinity purified by Protein A
交叉反应:hu, mo, rat, dog, Horse
产品介绍:The Hox homeobox genes encode proteins that are transcriptional regulators with an established role in embryonic development. HoxA6 (homeobox A6), also known as HOX1B, is a 233 amino acid protein that localizes to the nucleus. Expressed during embryonic development, HoxA6 functions as a sequence-specific DNA-binding transcription factor that is part of a regulatory mechanism that provides cells with positional identities during development. Via its ability to bind DNA, HoxA6 plays an important role in the regulation of gene expression, as well as morphogenesis and differentiation. The gene encoding HoxA6 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome.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.Tissue Specificity : Nucleus.Similarity : Belongs to the Antp homeobox family.Contains 1 homeobox DNA-binding domain.