久久99国产这里只有精品/欧美黄片大全/男生晚上睡不着想看点害羞的/小可爱免费直播下载 - 久色网

首頁 ? GM15989奈梅亨骨折綜合癥 |奈梅亨斷裂綜合癥基因; NBS1 皮膚,未特指成纖維細胞Cell Line細胞株-BioVector NTCC細胞庫

GM15989奈梅亨骨折綜合癥 |奈梅亨斷裂綜合癥基因; NBS1 皮膚,未特指成纖維細胞Cell Line細胞株-BioVector NTCC細胞庫

  • 價  格:¥98950
  • 貨  號:NTCC?---GM15989
  • 產  地:北京
點擊詢問我要采購
 竭誠為您服務!
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細胞名稱:NTCC? GM15989 NIJMEGEN BREAKAGE SYNDROME | NIJMEGEN BREAKAGE SYNDROME GENE; NBS1 Skin, Unspecified Cell Line
奈梅亨斷裂綜合癥 |奈梅亨斷裂綜合癥基因;國家統計局1細胞株
Description描述:The SV40 Transformed precrisis derivative of GM07166, a skin fibroblast strain established from a child diagnosed initially as having severe combined immunodeficiency and chromosome breakage syndrome (Conley et al, Blood 67:1251-1256,1986) later distinguished as genetically separate from ataxia-telangiectasia (Wegner et al, Clinical Genetics 33:20-32,1988; Jasper et al, Am J Hum Genet 42:66-73,1988), but showing similar x-ray sensitivity to ataxia telangiectasia (Jaspers et al, Cytogenet Cell Genet 49:259-263,1988); in 1998 GM07166 was identified as Nijmegen breakage syndrome carrying the Slavic mutation: deletion of 5bp at nucleotide 657 in exon 6 of the NBS1 gene resulting in premature termination at codon 218 [657-661delACAAA (657del5)] (Vason et al, Cell 93:467-476,1998); the chromosome counts vary from near diploid to near triploid to near tetraploid; the number of structural chromosome aberrations varies from 2 per cell in the near diploids to 17 per cell in the near tetraploids; it is not clear that any of the marker chromosomes recur in any of the cells; massive numbers of aberrations that are not clonal cannot be dealt with by the ISCN; it is to be expected that an SV40 transformant of a cell line from a donor with a chromosome instability syndrome is unstable with respect to both chromosome number and structural integrity
Category分類:Fibroblast
ID編號:NTCC?-GM15989
Size/Quantity數量: 1 Flask/2 Vials
Biosafety Level生物安全級別:1
Shipping Info運輸方式: RT/Dry Ice
Storage儲存方式: RT/Liquid Nitrogen
Race: White
Age年齡:20 YR
Gender性別:Female
Cell Type細胞類型: NIJMEGEN BREAKAGE SYNDROME | NIJMEGEN BREAKAGE SYNDROME GENE; NBS1
Affected State:Yes
Product:Fibroblast
Gene:NBS1
Mutations突變:5-BP DEL, NT657-661
Ethnicity:
Family:2100
Relationship:proband
Karyotype:
Tissue Type組織來源:Skin
Complete Growth Medium完全培養基: BioVector? Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent Complete Medium
Subculturing傳代方法:
Cryopreservation凍存方法:Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO
Storage temperature: liquid nitrogen vapor phase
Culture Conditions培養條件:Atmosphere: air, 95%; carbon dioxide (CO2), 5%
Temperature: 37.0°C
STR Profile鑒定數據:
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

您正在向 biovector.net  發送關于產品 GM15989奈梅亨骨折綜合癥 |奈梅亨斷裂綜合癥基因; NBS1 皮膚,未特指成纖維細胞Cell Line細胞株-BioVector NTCC細胞庫 的詢問

點擊“立即發送”后,我們將在1個工作日內與您取得聯系。