NTCC® NA08894 LCL DNA-BioVector NTCC典型培养物保藏中心Coriell NA08894
- 价 格:¥59850
- 货 号:NTCC®-Coriell NA08894
- 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® NA08894 LCL DNA
Category分类:DNA
Cat#货号:NTCC®-Coriell NA08894
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:
Gender性别: Male
Description描述: NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III; HSAN3 | INHIBITOR OF KAPPA LIGHT POLYPEPTIDE GENE ENHANCER IN B CELLS, KINASE-COMPLEX ASSOCIATED PROTEIN; IKBKAP
Remarks: Clinically affected; recurrent pneumonia; restrictive lung disease; azotemia; below 3rd percentile for height; persistent anemia possibly due to chronic blood loss from esophagitis; oropharyngeal incoordination with misdirection of fluids and foods with a watery consistency; gastroesophageal reflux; hypotension; chronic dehydration; nocturnal enuresis; alacrima; no corneal problems; divergent left exotropia; optic pallor; right thoracic kyphoscoliosis; bilateral pronated feet; history of seizures; history of fractures; tires easily; affected siblings are GM08895, GM08896; mother is GM08893; father is GM08892; donor subject is homozygous for the 2507+6T>C mutation in the IKBKAP gene; this donor splice site mutation (IVS20+6T>C) leads to deletion of exon 20 from the mRNA
Alternate IDs其他编号:
Cell Type细胞类型: LCL
Source组织来源: LCL
Gene: IKBKAP
Disease疾病类型:
Mutations突变: c.2204+6T>C (IVS20+6T>C)
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 NA08894
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:
Gender性别: Male
Description描述: NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III; HSAN3 | INHIBITOR OF KAPPA LIGHT POLYPEPTIDE GENE ENHANCER IN B CELLS, KINASE-COMPLEX ASSOCIATED PROTEIN; IKBKAP
Remarks: Clinically affected; recurrent pneumonia; restrictive lung disease; azotemia; below 3rd percentile for height; persistent anemia possibly due to chronic blood loss from esophagitis; oropharyngeal incoordination with misdirection of fluids and foods with a watery consistency; gastroesophageal reflux; hypotension; chronic dehydration; nocturnal enuresis; alacrima; no corneal problems; divergent left exotropia; optic pallor; right thoracic kyphoscoliosis; bilateral pronated feet; history of seizures; history of fractures; tires easily; affected siblings are GM08895, GM08896; mother is GM08893; father is GM08892; donor subject is homozygous for the 2507+6T>C mutation in the IKBKAP gene; this donor splice site mutation (IVS20+6T>C) leads to deletion of exon 20 from the mRNA
Alternate IDs其他编号:
Cell Type细胞类型: LCL
Source组织来源: LCL
Gene: IKBKAP
Disease疾病类型:
Mutations突变: c.2204+6T>C (IVS20+6T>C)
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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