NTCC® NA17583 LCL DNA-BioVector NTCC典型培养物保藏中心Coriell NA17583
- 价 格:¥59850
- 货 号:NTCC®-Coriell NA17583
- 产 地:北京
- BioVector NTCC典型培养物保藏中心
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地址:北京
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Name:NTCC® NA17583 LCL DNACategory分类:DNACat#货号:NTCC®-Coriell NA17583Size/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: 7 YRGender性别: FemaleDescription描述: RETT SYNDROME; RTT | METHYL-CPG-BINDING PROTEIN 2; MECP2Remarks: Clinically affected; also has triple X syndrome; normal growth parameters at birth; weak suck and poor weight gain in first few weeks of life; intestinal malrotation at 4 months; psychomotor development normal until 9 months when development slowed; walked at 16 months; head circumference and weight decreased at 6 months of age; regression of social skills evident at 20 months of age; bruxism, constipation and decreased sensitivity to pain developed at 21 months of age; significant delay in language development; no language and limited functional use of hands at age 6; MRI of cranium normal; EEG performed at 44 months showed intermittent occurence of epileptiform discharges, suggestive of partial seizures; supernumerary X chromosome is maternally derived; X-inactivation studies indicated preferential inactivation of the paternal allele; parental origin of MECP2 mutation could not be determined; donor subject has one allele that has a C>G transversion in the MBD coding region of the gene encoding methyl-CpG binding protein 2 (MECP2) resulting in a substitution of a valine for a leucine at codon 100 [Leu100Val (L100V)].Alternate IDs其他编号: Cell Type细胞类型:
LCLSource组织来源: LCLGene: MECP2 Disease疾病类型: Mutations突变: LEU100VALKaryotypes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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