重组JHDM1D蛋白
交货期：1周
产品别名：Recombinant KDM7A
Recombinant lysine demethylase 7A protein
Recombinant lysine demethylase 7A protein
基因名：
产品别名：
背景信息：
KDM7A
产品别名：
JHDM1D； KDM7A； lysine demethylase 7A； lysine demethylase 7A； lysine-specific demethylase 7A； [histone H3]-dimethyl-L-lysine9 demethylase 7A； histone lysine demethylase JHDM1D； jmjC domain-containing histone demethylation protein 1D； jumonji C domain containing histone demethylase 1 homolog D； lysine (K)-specific demethylase 7A； lysine-specific demethylase 7； JHDM1D蛋白；
背景信息：
JHDM1D is a 941 amino acid protein belonging to the JHDM1 histone demethylase family. Existing as two alternatively spliced isoforms, JHDM1D contains one JmjC domain and a PHD-type zinc finger. The gene encoding JHDM1D 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, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
产品发布日期：2026.01.29
广州伟伯科技有限公司