NTCC® NA25151 LCL DNA-BioVector NTCC典型培养物保藏中心Coriell NA25151
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- 货 号:NTCC®-Coriell NA25151
- 产 地:北京
- BioVector NTCC典型培养物保藏中心
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Name:NTCC® NA25151 LCL DNACategory分类:DNACat#货号:NTCC®-Coriell NA25151Size/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: 16 YRGender性别: FemaleDescription描述: NEMALINE MYOPATHY 2, AUTOSOMAL RECESSIVE; NEM2Remarks: Clinically affected; diagnosed at age 5 years; symptom onset at birth; high arched palate; very weak suck; swallowing dysfunction; aspiration; failure to thrive; motor delay; skeletal muscle weakness; respiratory weakness; drooling; speech impairment; maximum motor function achieved: climb 4 stairs with handrail; electron microscopy result: biopsy of the left gluteus muscle showed chronic myopathy with excessive accumulation of rod structures, indicative of nemaline rod myopathy, and fatty replacement within the muscle; NEB gene sequencing test result: heterozygous in the NEB gene for a mutation defined as c.3252_3255+3delTGACGTA, which includes the terminal four nucleotides of exon 32 and the first three nucleotides of intron 32, this region covers the conserved GT splice donor signal; array comparative genomic hybridization (aCGH) test result: heterozygous for ~2.7 kb deletion within the NEB gene encompassing exon 77 with genomic locations 152,469,299 in intron 77 and 152,471,995 in intron 76 (GRCh37/hg19); management: physical therapy, occupational therapy, psychological therapy and speech language therapy; surgeries:pharyngeal flap, g-tube, and tonsillectomy; medications: l-tyrosine + l-carnitine, Miralax, Prilosec, mesalamine; assistive devices: wheelchair, orthotics, service animal, respiratory support used at night.Alternate IDs其他编号: Cell Type细胞类型:
LCLSource组织来源: LCLGene: NEB Disease疾病类型: Mutations突变: c.3252_3255+3DELTGACGTA del encompassing exon 77Karyotypes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
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