半岛bd体育手机客户端 介绍
目录号 Serial |
SCSP-223 |
标识符 Identifier |
CSTR:19375.09.3101MOUSCSP223 |
描述 Description |
R1细胞系建系于1991年8月,取材于两个129亚品系(129S1/SvImJ and 129X1/SvJ)交配获得的3.5天囊胚。R1的多能性最初通过四倍体胚胎检测,当然也可以用二倍体胚胎检测。然而,当进行四倍体聚集体检测时,来自第14代的约20%的亚克隆具有R1的原始发育潜能。R1衍生的动物成年后可育。将经过基因改造的R1细胞注射到C57囊胚中或将其与CD-1或远交系ICR 8细胞期胚胎聚集,可以产生高效的生殖系传递。90%以上敲除克隆通过聚集嵌合体进入生殖系(n> 60)。每个批次均通过本库支原体检测,结果为阴性。冻存时为P22代。 |
动物种别 Organism |
小鼠,129X1×129S1品系 |
性别 Gender |
雄性 |
组织来源 Tissue and Cell Type |
小鼠胚胎内细胞团 |
形态 Morphology |
球形克隆,贴壁生长 |
培养基和添加剂 Complete Growth Medium and Culture Conditions |
mES完全培养液配方(600 ml): DMEM (Invitrogen 12430) 497 ml ES级FBS (biochrom S4115) 90 ml Glutamax (Invitrogen 35050) 6 ml NEAA (Invitrogen 11140) 6 ml LIF (Millipore ESG1107) 60 μl(终浓度为1000U/ml) β-Mer (Invitrogen 21985) 1.5 ml 气相:空气,95%;二氧化碳,5%。温度:37摄氏度。 |
供应限制 Permits and Restrictions |
A。仅供研究之用。 |
REFERENCE |
Matise M, et alProduction of targeted embryonic stem cell clonesIn: Matise M, et alGene Targeting: A Practical ApproachOxfordOxford University Press101-132, 1999Nagy A, et al. Derivation of completely cell culture-derived mice from early-passage embryonic stem cells. Proc. Natl. Acad. Sci. USA : 8424-8428, 1993. PubMed: 8378314Wood SA, et al. Non-injection methods for the production of embryonic stem cell-embryo chimaeras. Nature 365: 87-89, 1993. PubMed: 8361547Nagy A, Rossant JProduction and analysis of ES-cell aggregation chimerasIn: Nagy A, Rossant JGene Targeting: A Practical ApproachOxfordOxford University Press177-206, 1999Hay RJ, Caputo JL, Macy, ML, Eds. (1992) ATCC Quality Control Methods for Cell Lines. 2nd edition, Published by ATCC.Caputo JL. Biosafety procedures in cell culture. J. Tissue Culture Methods 11:223-227, 1988Fleming, D.O., Richardson, J. H., Tulis, J.J. and Vesley, D., (1995) Laboratory Safety: Principles and Practice. Second edition, ASM press, Washington, DC. |
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