细胞培养基 >> 细胞株
C3H/10T1/2, Clone 8小鼠纤维原细胞
产品介绍 目录号 Serial | SCSP-506 | 标识符 Identifier | CSTR:19375.09.3101MOUSCSP506 | 描述 Description | 这株细胞由C. Reznikoff、D. Brankow和C. Heidelberger于1972年从C3H系小鼠胚胎细胞中分离而来。建系人建议在P15前使用。该细胞为接触抑制型,在同源小鼠中不产生肿瘤,无自然转化的背景,也不含有明显的内源性转化鼠类白血病或肉瘤病毒。该细胞易于转染,容易被化学试剂转化。为了保持细胞原有的特性,应严格控制该细胞的接种密度、培养和传代周期。血清批次间的差异有可能影响细胞形态和细胞转染等实验结果。据报道,鼠痘病毒(ectromelia virus,ECTV)检测结果为阴性。本库冻存时为P10。 细胞质控结果: 1.支原体检测结果:每个批次均通过本库支原体检测,结果为阴性。 2.STR鉴定结果: ①该株细胞DNA进行小鼠细胞STR分型结果显示,扩增后图谱清晰,分型结果良好:1-1:10;1-2:16;2-1:9;3-2:14;4-2:20.3;5-5:15;6-4:18;6-7:12;7-1:26;8-1:15;11-2:16;12-1:16;13-1:17.1;15-3:25.3;17-2:14;18-3:16;19-2:12;X-1:26。 ②该株细胞确为小鼠细胞,没有人源细胞污染。 | 动物种别 Organism | 小鼠,C3H品系 | 性别 Gender | | 组织来源 Tissue and Cell Type | 胚胎 | 形态 Morphology | 成纤维细胞,贴壁生长 | 培养基和添加剂 Complete Growth Medium and Culture Conditions | MEM (Invitrogen, 11090081) 87 ml FBS (Gibco) 10 ml Glutamax(invitrogen 35050061) 1 ml SODIUM PYRUVATE SOL(invitrogen 11360070) 1 ml Non-essential Amino Acids, 100×(Invitrogen, 11140050) 1 ml 气相:空气,95%;二氧化碳,5%。温度:37摄氏度。 参考传代周期:必须在细胞交汇前传代 参考传代比例:2000个细胞/平方厘米 参考换液频率:如有需要,可在两次传代之间换一次液 冻存液配方:完全培养液95%,DMSO 5% | 供应限制 Permits and Restrictions | A。仅供研究之用。 | REFERENCE | Reznikoff CA, et al. Quantitative and qualitative studies of chemical transformation of cloned C3H mouse embryo cells sensitive to postconfluence inhibition of cell division. Cancer Res. 33: 3239-3249, 1973. PubMed: 4796800Terzaghi M, Little JB. Repair of potentially lethal radiation damage in mammalian cells is associated with enhancement of malignant transformation. Nature 253: 548-549, 1975. PubMed: 1167940Mondal S, Heidelberger C. Transformation of C3H/10T1/2 CL8 mouse embryo fibroblasts by ultraviolet irradiation and a phorbol ester. Nature 260: 710-711, 1976. PubMed: 1264242Smith GJ, et al. Clonal analysis of the expression of multiple transformation phenotypes and tumorigenicity by morphologically transformed 10T1/2 cells. Cancer Res. 53: 500-508, 1993. PubMed: 8425183Rapp UR, et al. Endogenous oncornaviruses in chemically induced transformation. I. Transformation independent of virus production. Virology 65: 392-409, 1975. PubMed: 165619Reznikoff CA, et al. Establishment and characterization of a cloned line of C3H mouse embryo cells sensitive to postconfluence inhibition of division. Cancer Res. 33: 3231-3238, 1973. PubMed: 4357355Jain MK, et al. Molecular cloning and characterization of SmLIM, a developmentally regulated LIM protein preferentially expressed in aortic smooth muscle cells. J. Biol. Chem. 271: 10194-10199, 1996. PubMed: 8626582 |
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