NTCC® NA01098 Fibroblast DNA-BioVector NTCC典型培养物保藏中心Coriell NA01098
- 价 格:¥59850
- 货 号:NTCC®-Coriell NA01098
- 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® NA01098 Fibroblast DNA
Category分类:DNA
Cat#货号:NTCC®-Coriell NA01098
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: 20 YR
Gender性别: Male
Description描述: COCKAYNE SYNDROME, TYPE B; CSB | EXCISION-REPAIR CROSS-COMPLEMENTING, GROUP 6; ERCC6
Remarks: Clinically affected; subject alternate ID is CS2BE or CS5HO; complementation group B; 46,XY; sensitive to UV irradiation; pigmentary retinopathy symptoms; gait defect; donor subject is a compound heterozygote: one allele has a 1 bp deletion at nucleotide 3614 in exon 18 of the ERCC6 gene (3614delT) causing a frameshift beginning at codon 1179 and ending with a stop codon at 1200 (1179fsX1200); the second allele has a deletion of exon 10 (del665_723); see GM01712 Lymphoid;
Alternate IDs其他编号:
Cell Type细胞类型: Fibroblast
Source组织来源: Fibroblast
Gene: ERCC6
Disease疾病类型:
Mutations突变: 3614delT DEL EX10
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 NA01098
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: 20 YR
Gender性别: Male
Description描述: COCKAYNE SYNDROME, TYPE B; CSB | EXCISION-REPAIR CROSS-COMPLEMENTING, GROUP 6; ERCC6
Remarks: Clinically affected; subject alternate ID is CS2BE or CS5HO; complementation group B; 46,XY; sensitive to UV irradiation; pigmentary retinopathy symptoms; gait defect; donor subject is a compound heterozygote: one allele has a 1 bp deletion at nucleotide 3614 in exon 18 of the ERCC6 gene (3614delT) causing a frameshift beginning at codon 1179 and ending with a stop codon at 1200 (1179fsX1200); the second allele has a deletion of exon 10 (del665_723); see GM01712 Lymphoid;
Alternate IDs其他编号:
Cell Type细胞类型: Fibroblast
Source组织来源: Fibroblast
Gene: ERCC6
Disease疾病类型:
Mutations突变: 3614delT DEL EX10
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
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