首页 » NTCC® NA25493 LCL DNA-BioVector NTCC典型培养物保藏中心Coriell NA25493

NTCC® NA25493 LCL DNA-BioVector NTCC典型培养物保藏中心Coriell NA25493

  • 价  格:¥59850
  • 货  号:NTCC®-Coriell NA25493
  • 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.

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

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Name:NTCC® NA25493 LCL DNA
Category分类:DNA
Cat#货号:NTCC®-Coriell NA25493
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: 8 YR
Gender性别: Female
Description描述: DEAFNESS, AUTOSOMAL RECESSIVE 1A; DFNB1A | GAP JUNCTION PROTEIN, BETA-2; GJB2 (CONNEXIN 26; CX26)
Remarks: Clinically affected; symptom onset at approximately age 3 or 4 years; diagnosed at age 6 years by a specialist (ENT/Audiology); bilateral sensorineural hearing loss that is severe in the lower frequencies rising to mild in the higher frequencies; history of chronic ear infections; noted issues with articulation; normal temporal bone CT; normal EKG; sequencing revealed that subject is homozygous for a c.11G>A mutation in the GJB2 gene resulting in p.Gly4Asp; subject also has a mitochondrial variant associated with non-syndromic hearing loss (mtDNA: 963T>C); normal SNP array: arr (1-22,X)x2 (Human Genome Build 37, hg19, 2009); assistive devices include: hearing aid; surgeries include: bilateral myringotomy and tube placement (BMT), tonsillectomy and adenoidectomy; Patient also has a mitochondrial variant associated with non-syndromic hearing loss: mtDNA:963T>C.
Alternate IDs其他编号:
Cell Type细胞类型: LCL
Source组织来源: LCL
Gene: GJB2
Disease疾病类型:
Mutations突变: GLY4ASP
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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