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四种传代细胞株软琼脂抛锚能力观察 被引量:1

Anchoring ability of 4 passage cells strain in soft-agar
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摘要 目的 观察传代细胞在软琼脂中生长情况 .方法 将4种细胞与软琼脂混合均匀 ,铺于平皿中 ,置 37℃ ,5 0~ 10 0m L·L- 1 CO2 环境中培养 .观察细胞集落形成情况 .结果 本实验室的五株非洲绿猴肾细胞 Vero- XAYU ,Vero- XAYE,Vero- XAH,Vero- XAJN和 Vero- XAM,三株猫肾细胞 F81 -XAJU,F81 - XAM和 F81 - XAK不呈现致瘤性独立抛锚生长 ;犬肾细胞 MDCK- XAYE,MDCK- XAYU,MDCK- XAJN,MD-CK- XAJA和 MDCK- XAM五株则呈现较低的致瘤性独立抛锚生长 ;两株金黄地鼠肾细胞 BHK2 1 - XAYU和 BHK2 1 - XAM及两株非洲绿猴肾细胞 Vero- XAYU和 Vero- AIM To observe the growth of passage cells in soft agar. METHODS Four kinds of passage cells were blended with soft agar and cultured at 37℃, 5%~10% CO 2 atmosphere and then the clone forming was observed. RESULTS Of the five strains of Vero XAYU, Vero XAYE, Vero XAH, Vero XAJN and Vero XAM in our laboratory, 3 strains of F 81 XAJU, F 81 XAM,and F 81 XAK grew anchor free without carcinogenesis, but 5 strains of MDCK XAYE,MDCK XAYU,MDCK XAJN,MDCK XAJA,and MDCK XAM grew anchor free with lower carcinogenesis; 2 strains of BHK 21 XAYu,BHK 21 XAM and another 2 strains of Vero XAYU,Vero XAK demonstrated an anchor free growth with high carcinogenesis.
出处 《第四军医大学学报》 2000年第6期736-737,共2页 Journal of the Fourth Military Medical University
基金 国家火炬计划 ![火炬发 ( 1997) 10 9号 ]
关键词 传代细胞系 克隆 克隆率 致瘤性 passage cell line clone clone ratio carcinogenesis
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参考文献4

  • 1王明俊,兽医生物制品学,1998年,5页
  • 2殷震,动物病毒学(第2版),1997年,467页
  • 3王衡文,实验肿瘤学基础,1992年,310页
  • 4汪希明,肿瘤生物学,1990年,213页

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  • 3Wilkins MR, Pasquali C, Appel RD, et al. From proteins to pro- teomes: large scale protein identification by two-dimensional elec- trophorcsis and amino acid analysis. Biotechnology (N Y), 1996, 14(1) : 61-65.
  • 4Chang WW, Huang L, Shen M, et al. Patterns of protein synthe- sis and tolerance of anoxia in root tips of maize seedlings acclima- ted to a low-oxygen environment, and identification of proteins by mass spectrometry. Plant Physiol, 2000, 122 (2) : 295-318.
  • 5Sheets R, Petricciani J. Vaccine cell substrates 2004. Expert Rev Vaccines, 2004, 3(6): 633-638.
  • 6Wolf JJ, Wang L, Wang F. Application of PCR technology in vac- cine product development. Expert Rev Vaccines, 2007, 6 ( 4 ) : 547 -558.
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