NTCC® NA21969 Fibroblast DNA-BioVector NTCC典型培养物保藏中心Coriell NA21969
- 价 格:¥59850
- 货 号:NTCC®-Coriell NA21969
- 产 地:北京
- BioVector NTCC典型培养物保藏中心
- 联系人:Dr.Xu, Biovector NTCC Inc.
电话:400-800-2947 工作QQ:1843439339 (微信同号)
邮件:Biovector@163.com
手机:18901268599
地址:北京
- 已注册
Name:NTCC® NA21969 Fibroblast DNA
Category分类:DNA
Cat#货号:NTCC®-Coriell NA21969
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: 45 YR
Gender性别: Female
Description描述: MARFAN SYNDROME; MFS | FIBRILLIN 1; FBN1
Remarks: Clinically affected; pectus carinatum; scoliosis; high narrow palate; contractures, including hammertoes; hypermobile small joints; hypermobile large joints; positive thumb sign; ascending aortic aneurysm; aortic dissection; aortic root replacement at age 42 years; mitral valve prolapse; mitral regurgitation; striae; donor subject has a 3 bp deletion and 20 bp insertion at nucleotide 1642 in exon 13 of the FBN1 gene (1642del3ins20) resulting in a premature stop codon [Ile578Ter (I578X)]
Alternate IDs其他编号:
Cell Type细胞类型: Fibroblast
Source组织来源: Fibroblast
Gene: FBN1
Disease疾病类型:
Mutations突变: 1642del3ins20
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
http://www.biovector.net
Category分类:DNA
Cat#货号:NTCC®-Coriell NA21969
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: 45 YR
Gender性别: Female
Description描述: MARFAN SYNDROME; MFS | FIBRILLIN 1; FBN1
Remarks: Clinically affected; pectus carinatum; scoliosis; high narrow palate; contractures, including hammertoes; hypermobile small joints; hypermobile large joints; positive thumb sign; ascending aortic aneurysm; aortic dissection; aortic root replacement at age 42 years; mitral valve prolapse; mitral regurgitation; striae; donor subject has a 3 bp deletion and 20 bp insertion at nucleotide 1642 in exon 13 of the FBN1 gene (1642del3ins20) resulting in a premature stop codon [Ile578Ter (I578X)]
Alternate IDs其他编号:
Cell Type细胞类型: Fibroblast
Source组织来源: Fibroblast
Gene: FBN1
Disease疾病类型:
Mutations突变: 1642del3ins20
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
http://www.biovector.net
- 公告/新闻