NTCC® NA17472 Fibroblast DNA-BioVector NTCC典型培养物保藏中心Coriell NA17472
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- 货 号:NTCC®-Coriell NA17472
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Name:NTCC® NA17472 Fibroblast DNACategory分类:DNACat#货号:NTCC®-Coriell NA17472Size/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: 13 YRGender性别: MaleDescription描述: ACYL-CoA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF | ACYL-CoA DEHYDROGENASE, SHORT-CHAIN; ACADSRemarks: Clinically affected; benign heart murmur; reactive airway disease; recurrent migraine headaches usually accompanied by a visual aura; noninflammatory myopathy; severe leg and calf pain after infections and exertion; acute episode of severe muscle cramping, contractions and pain associated with elevated CPK levels in serum occurred at age 8 years; at the time of this acute episode the total carnitine was 22.5 (normal 33.9-69) and free carnitine was 18.7 (normal 30.2-56.8); recurrent rhabdomyolysis; light microscopy performed on muscle biopsy was normal; 50% of normal carnitine palmitoyl transferase II activity; normal small-chain Acyl-CoA dehydrogenase activity in fibroblasts and muscle; fibroblast oxidation studies showed marked elevation of butylcarnitine; elevation of butyryl carnitine after MCT load consistent with a partial defect in short-chain acyl-Co-A dehydrogenase deficiency; ethylmalonic acid level was normal in urine; donor subject is a compound heterozygote: one allele has a G>A transition at nucleotide 625 of the ACADS gene [625G>A] resulting in a substitution of serine for glycine at codon 185 [Gly185Ser (G185S)] and a second allele has a C>T transition at nucleotide 511 of the ACADS gene [511C>T] resulting in a substitution of tryptophan for arginine at codon 147 [Arg147Trp (R147W)].Alternate IDs其他编号: Cell Type细胞类型:
FibroblastSource组织来源: FibroblastGene: ACADS Disease疾病类型: Mutations突变: ARG147TRP GLY185SERKaryotypes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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