期刊文献+

RNAiFect^(TM)和SuperFect转染试剂对4种细胞活性的影响 被引量:2

The lnfluence on the four kinds of cells by adding RNAiFect^(TM) and super fect
下载PDF
导出
摘要 在RNA干涉中,转染试剂的用量与siRNAs的量成正相关关系,但因转染试剂对细胞有一定的毒性作用,超过一定用量可以引起细胞形状改变、脱落、甚至死亡,直接影响着干涉的效率,所以确定转染试剂的优化用量,是RNA干涉试验中的重要环节.将不同用量的RNA iFectTM和SuperFect两种转染试剂分别加入鸡胚成纤维(CEF)细胞、293细胞、PK细胞和MDCK细胞中,在4h和24h后观察细胞的活力情况,比较了不同转染试剂对不同细胞的影响.结果表明:相同用量的两种转染试剂对293细胞、PK细胞和MDCK细胞的生长的影响远远小于对CEF细胞的影响;两种转染试剂用于外源小分子转染时,建议在293细胞、PK细胞和MDCK细胞上的用量不超过3u l;两种转染试剂对CEF细胞的毒性较大,不适合用于转染. In the RNA interference,the dosage of siRNAs has positive correlativity with that of transfection reagent.However,transfection reagents have a great influence on the growth of cells,including cells falling off,morphological change,even dying,etc.,when the dosage of the transfection reagent exceeds to some extend.So it is a very important process to RNA interference that ascertaining the optimization dosage of transfection reagent.In the test,the author added different dosages of two transfection reagents R...
出处 《西南民族大学学报(自然科学版)》 CAS 2005年第S1期53-56,共4页 Journal of Southwest Minzu University(Natural Science Edition)
基金 四川省应用基础课题(05JY029-007-5) 四川省畜牧食品局资助项目
关键词 RNAiFectTM转染试剂 SuperFect转染试剂 鸡胚成纤维细胞 293细胞 PK细胞 MDCK细胞 毒性 RNAiFect^(TM)Transfection Reagent SuperFect Transfection Reagent CEF cell 293 cell PK cell MDCK cell toxicity
  • 相关文献

参考文献2

二级参考文献22

  • 1B.Q. Jiang, L. Gu,W.L. Zhang,Y.S. Sun and F. Lin Chemical Engineering Department of Nanchang University, Nanchang 330029, China.PREPARATION OF SILICA MOLECULAR SIEVE MEMBRANE FOR HYDROGEN SEPARATION[J].Acta Metallurgica Sinica(English Letters),1999,12(5):1077-1081. 被引量:1
  • 2Alvarado AS, Newmark PA, 1999. Double-stranded RNA specifically disrupts gene expression during planarian regeneration. Proc.Natl. Acad. Sci. USA 96:5 049-5 054.
  • 3Bernstein E, Hammond SM, Hannon GJ, 2001. Role for a bidentate ribonuclease in the initiation step of RNA interference. Nature 409(6 818): 363 - 366.
  • 4Billy E, Zhang HD, Filipowicz W, 2001. Specific interference with gene expression induced by long, double-stranded RNA in mouse embryonal teratocarcinoma cell lines. Proc. Natl. Acad. Sci. USA 98 (25): 14 428- 14 433.
  • 5Chalfie M, Tu Y, Euskirchen G, 1994. Green fluorescent protein as a marker for gene express. Science 263: 802 - 805.
  • 6Chuang C, Meyerowitz EM, 2000. Specific and heritable genetic interference by double-stranded RNA in Arabidopsis thaliana. Proc.Natl. Acad. Sci. USA 97 (9): 4 985-5 054.
  • 7Cogoni C, Macino G, 1999. Gene silencing in Neurospora crassa requires a protein homologous to RNA-dependent RNA polymerase.Nature 399 (6 732): 166- 169.
  • 8Elbashir SM, Lendeckel W, Tuschl T, 2001. Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells. Nature 411 (6 836): 428-429.
  • 9Fire A, Xu S, Montgomery MK, Kostas SA, Driver SE, Mello CC,1998. Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans. Nature 391 (6 669): 806-811.
  • 10Fraser AG, Kamath RS, Zipperlen P, Campos MM, Sohrmann M,Ahringer J, 2000. Functional genomic analysis of C. elegans chromosome Ⅰ by systematic RNA interference. Nature 408: 325-330.

共引文献10

同被引文献38

引证文献2

二级引证文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部