产品介绍 目录号 Serial | SCSP-5036 | 标识符 Identifier | CSTR:19375.09.3101MOUSCSP5036 | 描述 Description | 该细胞株建自Abelson小鼠白血病病毒诱发的肿瘤组织,是科研上最常用的炎症细胞模型之一。该细胞易于增殖,高效DNA转染力,对RNA干扰敏感,常用作转染宿主细胞和复制小鼠诺如病毒。该细胞表面sIg-、Ia-、Thy-1.2抗原阴性。据报道,该细胞建系后已不分泌且检测不到病毒颗粒,XC斑点形成实验阴性。可以抗体依赖性地分解绵羊红血球与肿瘤靶细胞,LPS或PPD处理2天后可诱导分解红血球但对肿瘤靶细胞无作用。经检测鼠痘病毒阴性。 质量控制: 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:1-1:16;1-2:17;2-1:16;3-2:14;4-2:22.3;5-5:14;6-4:17,18;6-7:12;7-1:25.2;8-1:13;11-2:17;12-1:16;13-1:16.2;15-3:22.3;17-2:14,16;18-3:18;19-2:14;X-1:24。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 | 性别 Gender | 雄性 | 组织来源 Tissue and Cell Type | Abelson鼠科白血病病毒诱导的肿瘤;腹水 | 形态 Morphology | 单核细胞样/巨噬细胞样,贴壁生长 | 培养基和添加剂 Complete Growth Medium and Culture Conditions | 小鼠白血病病毒诱发肿瘤巨噬细胞RAW 264.7完全培养液配方(100 ml): DMEM (Invitrogen, 11960-044) 88 ml Glutamax (Invitrogen, 35050061) 1 ml Sodium Pyruvate 100 mM Solution (Invitrogen, 11360070) 1 ml FBS (Gibco) 10 ml 气相:空气95%,二氧化碳5%;37℃培养。 参考传代周期:3-5天 参考传代比例:1:3-1:6 参考换液频率:2-3天 冻存液配方:完全培养液95%,DMSO 5% 生物安全等级:BSL-2 注意事项: (1)该细胞传代时不需要用胰酶消化。传代时,吸走部分培养液,留下少许培养液(例如使用T75培养瓶则留下10 ml),用无菌细胞刮刮拭培养表面将细胞刮落,充分吹打后接种到新的装有新鲜培养液+的培养瓶内,混匀。 (2)在正常培养条件下,未经诱导分化的RAW264.7细胞形态上呈现松散贴壁的纺锤形和圆形或者立方形。当细胞密度较大时,细胞会轻微脱落变圆或者许多细胞堆积在一起,有些细胞甚至脱落漂浮。这些漂浮的细胞是存活的,在传代时应收集起来,离心后细胞沉淀可以继续培养。 (3)血清质量差异可能引起细胞贴壁能力变化,应选用高质量的胎牛血清。 | 供应限制 Permits and Restrictions | A。仅供研究之用。 | REFERENCE | Ralph P, Nakoinz I. Antibody-dependent killing of erythrocyte and tumor targets by macrophage-related cell lines: enhancement by PPD and LPS. J. Immunol. 119: 950-954, 1977. PubMed: 894031</br>Raschke WC, et al. Functional macrophage cell lines transformed by Abelson leukemia virus. Cell 15: 261-267, 1978. PubMed: 212198</br>Denlinger LC, et al. Regulation of inducible nitric oxide synthase expression by macrophage purinoreceptors and calcium. J. Biol. Chem. 271: 337-342, 1996. PubMed: 8550583<br />Hambleton J, et al. Activation of c-Jun N-terminal kinase in bacterial lipopolysaccharide-stimulated macrophages. Proc. Natl. Acad. Sci. USA 93: 2774-2778, 1996. PubMed: 8610116<br />Taylor GA, et al. Identification of anovel GTPase, the inducibly expresed GTPase, that accumulates in response to interferon gamma. J. Biol. Chem. 271: 20399-20405, 1996. PubMed: 8702776<br />Li YM, et al. Molecular identity and cellular distribution of advanced glycation endproduct receptors: relationship of p60 to OST-48 and p90 to 80K-H membrane proteins. Proc. Natl. Acad. Sci. USA 93: 11047-11052, 1996. PubMed: 8855306<br />Panneerselvam K, Freeze HH. Mannose enters mammalian cells using a specific transporter that is insensitive to glucose. J. Biol. Chem. 271: 9417-9421, 1996. PubMed: 8621609<br />Lokuta MA, et al. Mechanisms of murine RANTES chemokine gene induction by newcatle disease virus. J. Biol. Chem. 271: 13731-13738, 1996. PubMed: 8662857<br />Taylor MF, et al. In vitro efficacy of morpholino-modified antisense oligomers directed against tumor necrosis factor-alpha mRNA. J. Biol. Chem. 271: 17445-17452, 1996. PubMed: 8663413<br />Standard Practice for Testing for Biological Responses to Particles in Vitro. West Conshohocken, PA:ASTM International;ASTM Standard Test Method F 1903-98R03.<br />Hartley JW, et al. Expression of infectious murine leukemia viruses by RAW264.7 cells, a potential complication for studies with a widely used mouse macrophage cell line. Retrovirology. 4: 5:1, 2008. PubMed 18177500.<br /> |
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