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重组SAMD9蛋白
半岛bd体育手机客户端
介绍 基因名: SAMD9 半岛bd体育手机客户端 别名: C7orf5; DRIF1; M7MLS2; MIRAGE; NFTC; OEF1; OEF2; SAMD9; sterile alpha motif domain containing 9; sterile alpha motif domain containing 9; sterile alpha motif domain-containing protein 9; SAM domain-containing protein 9; expressed in aggressive fibromatosis; SAMD9蛋白; 背景信息: Defects in SAMD9 are the cause of normophosphatemic familial tumoral calcinosis (NFTC). NFTC is an uncommon life-threatening disorder characterized by massive periarticular, and seldom visceral, deposition of calcified tumors. 标签:His-tag |
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