首页 » NTCC® NA16192 Fibroblast DNA-BioVector NTCC典型培养物保藏中心Coriell NA16192

NTCC® NA16192 Fibroblast DNA-BioVector NTCC典型培养物保藏中心Coriell NA16192

  • 价  格:¥59850
  • 货  号:NTCC®-Coriell NA16192
  • 产  地:北京
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BioVector NTCC典型培养物保藏中心
联系人:Dr.Xu, Biovector NTCC Inc.

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Name:NTCC® NA16192 Fibroblast DNA
Category分类:DNA
Cat#货号:NTCC®-Coriell NA16192
Size/Quantity数量: 1 Vial
Biosafety Level生物安全级别:1
Shipping Info运输方式: RT
Storage储存方式: 4C
Species物种来源:
Age年龄: 1 MO
Gender性别: Male
Description描述: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4 (WALKER-WARBURG SYNDROME INCLUDED) | FUKUTIN; FKTN
Remarks: Clinically affected; foreskin; type II lissencephaly; congenital myotonic dystrophy; hydrocephalus indicated in utero by MRI; no aqueductal stenosis by post-natal MRI/CT; vermis hypoplasia; absent septum pellucidum; CPK = 2,200 u/ml; retinal exam showed vitreous hemorrhage but no pigmentary retinopathy; hypertonia; karyotype is 46,XY.ish 17(LIS1x2,RARAx2); donor is a compound heterozygote: one allele has a 1 bp deletion at nucleotide 385 in exon 5 of the FKTN gene (c.385delA) resulting in a frameshift and creation of a stop at codon 129 (I129fsX1); the second allele has a C>A transversion at nucleotide 1176 in exon 10 (c.1176C>A) resulting in a stop at codon 392 [Tyr392Ter (Y392X)]
Alternate IDs其他编号:
Cell Type细胞类型: Fibroblast
Source组织来源: Fibroblast
Gene: FKTN
Disease疾病类型:
Mutations突变: 385delA TYR392TER
Karyotypes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
Tel电话:400-800-2947
Email:Biovector@163.com
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