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7号染色体开放阅读框46抗体
产品名称 Anti-Fam221a Anti-family with sequence similarity 221, member A Antibody 产品介绍
靶标: Fam221a 产品别名: D330028D13Rik; Fam221a; family with sequence similarity 221, member A; family with sequence similarity 221, member A; protein FAM221A; uncharacterized protein C7orf46 homolog; 7号染色体开放阅读框46; 背景信息: Chromosome 7 has 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. The C7orf46 gene product has been provisionally designated C7orf46 pending further characterization. |
广州伟伯科技有限公司
手机: 13533759269 传真: 020-36393398 联系人: 林生 邮编: 362011 地址: 广州市白云区石井石槎路金碧新城5栋904室 相关产品:
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