NTCC? NA22090 LCL DNA-BioVector NTCC典型培養物保藏中心Coriell NA22090
- 價 格:¥59850
- 貨 號:NTCC?-Coriell NA22090
- 產 地:北京
- BioVector NTCC典型培養物保藏中心
- 聯系人:Dr.Xu, Biovector NTCC Inc.
電話:400-800-2947 工作QQ:1843439339 (微信同號)
郵件:Biovector@163.com
手機:18901268599
地址:北京
- 已注冊
Name:NTCC? NA22090 LCL DNA
Category分類:DNA
Cat#貨號:NTCC?-Coriell NA22090
Size/Quantity數量: 1 Vial
Biosafety Level生物安全級別:1
Shipping Info運輸方式: RT
Storage儲存方式: 4C
Species物種來源:
Age年齡:
Gender性別: Male
Description描述: PELIZAEUS-MERZBACHER-LIKE DISEASE, TYPE UNKNOWN
Remarks: Clinically affected; presents with PMD-like symptoms; born after full term pregnancy with no complications to healthy, unrelated Ashkenazi Jewish parents; was irritable and "colicky" as an infant; never developed normal sleep patterns; did not develop motor milestones by age 3 months; subject was negative for storage and metabolic abnormalities; speech delay: non-verbal but able to understand and be receptive of language; severe visual impairment due to optic atrophy, but no abnormal eye movements; spasticity; dysphagia; severely exaggerated gag reflex; active bite reflex-often bit his own lower lip; severe reflux; severely underweight; vomited nearly daily, frequent GI illness; minimal pubertal development: onset of pubic hair, slight enlargement of penis, no facial hair and voice did not change; failure to thrive; reactive airway disease; died suddenly at age 17; Analysis of PCR-based automated fluorescent sequencing of the 5' untranslated region, the intron-exon junction, and the coding region of the GJA12 gene detected a heterozygous base change c.966G>C in the GJA12 gene that does not result in amino acid changes; no mutations in GJA12 that would result in amino acid changes were detected; no duplications or mutations of the PLP gene were detected using multiplex PCR amplification and PCR-based automated fluorescent sequencing; whole exome sequencing of DNA revealed no pathogenic mutations in PLP1, GJC2, AIMP1, HSPD1, FAM126A, TUBB4A, POLR3A, POLR3B, or ALC16A2; treatments included: H2 blockers, nebulized Albuterol, and Baclofen; deceased affected sister (GM22060, fibroblast).
Alternate IDs其他編號:
Cell Type細胞類型: LCL
Source組織來源: LCL
Gene:
Disease疾病類型:
Mutations突變:
Karyotypes核型:
Cytogenetics:
Mutation description突變描述:
Origin:
Transformants:
Alias別名:
Images圖片:
References參考文獻:
Supplier供應商:
BioVector質粒載體菌株細胞蛋白抗體基因保藏中心
NTCC典型培養物保藏中心
Tel電話:400-800-2947
Email:Biovector@163.com
http://www.biovector.net
Category分類:DNA
Cat#貨號:NTCC?-Coriell NA22090
Size/Quantity數量: 1 Vial
Biosafety Level生物安全級別:1
Shipping Info運輸方式: RT
Storage儲存方式: 4C
Species物種來源:
Age年齡:
Gender性別: Male
Description描述: PELIZAEUS-MERZBACHER-LIKE DISEASE, TYPE UNKNOWN
Remarks: Clinically affected; presents with PMD-like symptoms; born after full term pregnancy with no complications to healthy, unrelated Ashkenazi Jewish parents; was irritable and "colicky" as an infant; never developed normal sleep patterns; did not develop motor milestones by age 3 months; subject was negative for storage and metabolic abnormalities; speech delay: non-verbal but able to understand and be receptive of language; severe visual impairment due to optic atrophy, but no abnormal eye movements; spasticity; dysphagia; severely exaggerated gag reflex; active bite reflex-often bit his own lower lip; severe reflux; severely underweight; vomited nearly daily, frequent GI illness; minimal pubertal development: onset of pubic hair, slight enlargement of penis, no facial hair and voice did not change; failure to thrive; reactive airway disease; died suddenly at age 17; Analysis of PCR-based automated fluorescent sequencing of the 5' untranslated region, the intron-exon junction, and the coding region of the GJA12 gene detected a heterozygous base change c.966G>C in the GJA12 gene that does not result in amino acid changes; no mutations in GJA12 that would result in amino acid changes were detected; no duplications or mutations of the PLP gene were detected using multiplex PCR amplification and PCR-based automated fluorescent sequencing; whole exome sequencing of DNA revealed no pathogenic mutations in PLP1, GJC2, AIMP1, HSPD1, FAM126A, TUBB4A, POLR3A, POLR3B, or ALC16A2; treatments included: H2 blockers, nebulized Albuterol, and Baclofen; deceased affected sister (GM22060, fibroblast).
Alternate IDs其他編號:
Cell Type細胞類型: LCL
Source組織來源: LCL
Gene:
Disease疾病類型:
Mutations突變:
Karyotypes核型:
Cytogenetics:
Mutation description突變描述:
Origin:
Transformants:
Alias別名:
Images圖片:
References參考文獻:
Supplier供應商:
BioVector質粒載體菌株細胞蛋白抗體基因保藏中心
NTCC典型培養物保藏中心
Tel電話:400-800-2947
Email:Biovector@163.com
http://www.biovector.net
- 公告/新聞