NTCC® NA25285 LCL DNA-BioVector NTCC典型培养物保藏中心Coriell NA25285
- 价 格：¥59850
- 货 号：NTCC®-Coriell NA25285
- 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® NA25285 LCL DNA
Category分类：DNA
Cat#货号:NTCC®-Coriell NA25285
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: 5 YR
Gender性别: Male
Description描述: CODAS SYNDROME | COAGULATION FACTOR V; F5 | LON PEPTIDASE 1, MITOCHONDRIAL; LONP1
Remarks: Clinically affected; diagnosed at 3 years of age; physical features: broad skull and flattened midface; ptosis; congenital cataracts causing visual impairment; grooved nasal tip; anteverted nares; small ears; helix hypoplasia (crumpled ears); bilateral hearing loss; pre-tragal cartilagenous bumps; high intact palate; paretic atrophic vocal cords; congenital stridor; laryngeal dysplasia (glottic narrowing); swallowing dysfunction; small patent foramen ovale; unilateral cryptorchidism; hypotonia; perennial rhinitis; environmental allergies; chronic sialorrhea causing aspiration and recurrent pneumonia; recurrent vomiting; spondoepi/metaphyseal dysplasia(skeletal survey at 1 year old shows abnormal cervical vertebrae and abnormal proximal/distal femurs); scoliosis of thoracolumbar spine (films at at 3 years of age show 45 degree curvature T2-T9 apex to the right); bilateral genu valgum; symmetric somatic and linear growth delay (5th percentile); subject ambulatory with walker by age 30 months; developmental delay; Sanger sequencing determined the subject to be homozygous for a c.2161C>G mutation in the LONP1 gene; subject is also heterozygous for the c.1601G>A mutation in the Factor 5 Leiden gene (determined by high resolution melting curve analysis) procedures include: tracheostomy, myringotomy; gastro-jejunal feeding (gastrostomy tube). [see publication by Strauss et al, PMID: 25574826].
Alternate IDs其他编号:
Cell Type细胞类型: LCL
Source组织来源: LCL
Gene: F5 LONP1
Disease疾病类型:
Mutations突变: c.1601G>A c.2161C>G
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 NA25285
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: 5 YR
Gender性别: Male
Description描述: CODAS SYNDROME | COAGULATION FACTOR V; F5 | LON PEPTIDASE 1, MITOCHONDRIAL; LONP1
Remarks: Clinically affected; diagnosed at 3 years of age; physical features: broad skull and flattened midface; ptosis; congenital cataracts causing visual impairment; grooved nasal tip; anteverted nares; small ears; helix hypoplasia (crumpled ears); bilateral hearing loss; pre-tragal cartilagenous bumps; high intact palate; paretic atrophic vocal cords; congenital stridor; laryngeal dysplasia (glottic narrowing); swallowing dysfunction; small patent foramen ovale; unilateral cryptorchidism; hypotonia; perennial rhinitis; environmental allergies; chronic sialorrhea causing aspiration and recurrent pneumonia; recurrent vomiting; spondoepi/metaphyseal dysplasia(skeletal survey at 1 year old shows abnormal cervical vertebrae and abnormal proximal/distal femurs); scoliosis of thoracolumbar spine (films at at 3 years of age show 45 degree curvature T2-T9 apex to the right); bilateral genu valgum; symmetric somatic and linear growth delay (5th percentile); subject ambulatory with walker by age 30 months; developmental delay; Sanger sequencing determined the subject to be homozygous for a c.2161C>G mutation in the LONP1 gene; subject is also heterozygous for the c.1601G>A mutation in the Factor 5 Leiden gene (determined by high resolution melting curve analysis) procedures include: tracheostomy, myringotomy; gastro-jejunal feeding (gastrostomy tube). [see publication by Strauss et al, PMID: 25574826].
Alternate IDs其他编号:
Cell Type细胞类型: LCL
Source组织来源: LCL
Gene: F5 LONP1
Disease疾病类型:
Mutations突变: c.1601G>A c.2161C>G
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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