供货周期: | 7天 |
品牌: | Coriell Institute |
货号: |
Coriell Institute 作为已被国际认可的权威机构,致力于为个性化医疗和干细胞生物学快速发展做出贡献。其中,Biobank的人类基因组DNA标准品,已广泛应用被国内各大知名基因公司及科研单位所信赖。比如,北京信诺佰世医学检验所、安诺优达基因科技(北京)有限公司、北京中仪康卫医疗器械有限公司、华大基因等。
其中,NA12878 在国内也已成为基因组测序行业的标准。例如,北京博奥晶典生物技术有限公司 10X Genomics全基因组重测序解决方案,用 NA12878 做的分型检测 (NA12878 trio分析)和NA12878的基因组缺失检测。
以NA12878 为例,展示如下:
NA12878 DNA from LCL
Description:
CEPH/UTAH PEDIGREE 1463 INTERNATIONAL HAPMAP PROJECT - CEPH (PLATE I) [UTAH RESIDENTS WITH ANCESTRY FROM NORTHERN AND WESTERN EUROPE]
CYTOCHROME P450, SUBFAMILY IIC, POLYPEPTIDE 19; CYP2C19
INTERNATIONAL HAPMAP PROJECT - CEPH [UTAH RESIDENTS WITH ANCESTRY FROM NORTHERN AND WESTERN EUROPE]
NA CUSTOM SERVICE PLATE 01
Affected: No Data
Gender: Female
Age: No Data
Repository: NIGMS Human Genetic Cell Repository
Subcollection: CEPH
Repository Linkage Families
Pharmacogenetics
PIGI Consented Sample
Quantity: 50 μg
Quantitation: MethodPlease see our FAQ
Biopsy Source: Peripheral vein
Cell Type: B-Lymphocyte
Tissue Type: Blood
Transformant: Epstein-Barr Virus
Race: Caucasian
Ethnicity: UTAH/MORMON
Country of Origin: USA
Family Member: 2
Relation to Proband: mother
Confirmation: Clinical summary/Case history
ISCN: 46,XX[23].arr[hg19] 9p13.1(38,787,480-40,911,212)x3
Species: Homo sapiens
Common Name: Human
Remarks:
Mother; donor subject has a single bp (G-to- A) transition at nucleotide 681 in exon 5 of the CYP2C19 gene (CYP2C19*2) which creates an aberrant splice site. The change altered the reading frame of the mRNA starting with amino acid 215 and produced a premature stop codon 20 amino acids downstream, resulting in a truncated, nonfunctional protein. Because of the aberrant splice site, a 40-bp deletion occurred at the beginning of exon 5 (from bp 643 to bp 682), resulting in deletion of amino acids 215 to 227. The truncated protein had 234 amino acids and would be catalytically inactive because it lacked the heme-binding region.
库存:NA12878、NA17195、NA00472、NA22031、NA16718、NA24385 、HG00096 等等
另有库存细胞:GM03576、GM04126、GM09596、GM10160、GM12878 等等
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