NTCC® NA02016 Fibroblast DNA-BioVector NTCC典型培养物保藏中心Coriell NA02016
- 价 格:¥59850
- 货 号:NTCC®-Coriell NA02016
- 产 地:北京
- BioVector NTCC典型培养物保藏中心
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Name:NTCC® NA02016 Fibroblast DNACategory分类:DNACat#货号:NTCC®-Coriell NA02016Size/Quantity数量: 1 VialBiosafety Level生物安全级别:1Shipping Info运输方式: RTStorage储存方式: 4CSpecies物种来源: Age年龄: 35 YRGender性别: FemaleDescription描述: HURLER-SCHEIE SYNDROME | CYTOCHROME P450, SUBFAMILY IID, POLYPEPTIDE 6; CYP2D6 | CYTOCHROME P450, SUBFAMILY IIC, POLYPEPTIDE 19; CYP2C19 | CYTOCHROME P450, SUBFAMILY IIC, POLYPEPTIDE 9; CYP2C9 | VITAMIN K EPOXIDE REDUCTASE COMPLEX, SUBUNIT 1; VKORC1 | UDP-GLYCOSYLTRANSFERASE 1 FAMILY, POLYPEPTIDE A1; UGT1A1Remarks: Clinically unaffected mother of affected child (GM01898); The following datasets were obtained and reported by the GeT-RM program: HLA variants (HLA-A*02:01/*30:02, HLA-B*53:01/*58:01, HLA-C*04:01/*07:01, HLA-DRB1*08:04/*14:01, HLA-DQB1*04:02/*05:01); pharmacogenomic variants ( CYP2D6*2XN/*17, CYP2C19*1/*2, CYP2C9*1/*1, VKORC1*WT/-1639G>A, UGT1A1*1/*1).
Alternate IDs其他编号: Cell Type细胞类型:
FibroblastSource组织来源: FibroblastGene: CYP2D6 Disease疾病类型: Mutations突变: DUP THR107ILE, ARG296CYS, AND SER486THRKaryotypes核型: Cytogenetics: Mutation description突变描述: Origin: Transformants: Alias别名: Images图片:References参考文献:Supplier供应商:BioVector质粒载体菌株细胞蛋白抗体基因保藏中心
NTCC典型培养物保藏中心
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