NTCC? NA05168 LCL DNA-BioVector NTCC典型培養物保藏中心Coriell NA05168
- 價 格:¥59850
- 貨 號:NTCC?-Coriell NA05168
- 產 地:北京
- BioVector NTCC典型培養物保藏中心
- 聯系人:Dr.Xu, Biovector NTCC Inc.
電話:400-800-2947 工作QQ:1843439339 (微信同號)
郵件:Biovector@163.com
手機:18901268599
地址:北京
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Name:NTCC? NA05168 LCL DNACategory分類:DNACat#貨號:NTCC?-Coriell NA05168Size/Quantity數量: 1 VialBiosafety Level生物安全級別:1Shipping Info運輸方式: RTStorage儲存方式: 4CSpecies物種來源: Age年齡: 28 YRGender性別: FemaleDescription描述: CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A; CMT1A | PERIPHERAL MYELIN PROTEIN 22; PMP22Remarks: Clinically affected; high arches of feet; difficulty with running as a teenager; marked equinus deformity of the foot with early hammer toes; marked weakness of the foot extensors; mildly reduced sensation to pin and light touch; walks with slight steppage gait; normal strength in bulk in upper extremities; normal strength of psoas, quadriceps, hamstrings, and gastrocnemius muscles; no palpably enlarged nerves noted peripherally; affected father is GM05166; EMG performed at age 28 was "compatible with a rather significant polyneuropathic process of a primary demyelinating type. The findings would be consistent with a clincial suspected diagnosis of Charcot-Marie-Tooth disease."; see GM05167 fibroblast; donor subject was found to have a duplication (17p) of the PMP22 gene by MLPA; no mutations were found in the MPZ gene; donor subject also has a homozygous polymorphism: IVS3+64T>C (rs6674383)Alternate IDs其他編號: Cell Type細胞類型:
LCLSource組織來源: LCLGene: PMP22 Disease疾病類型: Mutations突變: DUP (17p)Karyotypes核型: Cytogenetics: Mutation description突變描述: Origin: Transformants: Alias別名: Images圖片:References參考文獻:Supplier供應商:BioVector質粒載體菌株細胞蛋白抗體基因保藏中心
NTCC典型培養物保藏中心
Tel電話:400-800-2947
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