首页> 美国卫生研究院文献>Journal of Experimental Clinical Cancer Research : CR >Correction to: Circ-ASH2L promotes tumor progression by sponging miR-34a to regulate Notch1 in pancreatic ductal adenocarcinoma
【2h】

Correction to: Circ-ASH2L promotes tumor progression by sponging miR-34a to regulate Notch1 in pancreatic ductal adenocarcinoma

机译:校正至:循环灰2L通过冲压miR-34a调节胰腺导管腺癌中的Notch1来促进肿瘤进展

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

a-b The invasion abilities of indicate treated Capan-1 (a) and Aspc-1 cells (b) were measured by transwell assays. Scale bars = 50 μm. c-d The proliferation abilities of indicate treated Capan-1 (c) and Aspc-1 cells (d) were measured by EdU assays. Scale bars = 50 μm. e-g The indicate treated Aspc-1 and Capan-1 cells (e) were stained by propidium iodide and analyzed using flow cytometry, the statistical results of Aspc-1 (f) and Capan-1 (g) cells were showed in right column. h-i The in vitro angiogenesis abilities of indicated treated Capan-1 and Aspc-1 cells were measured by tube-formation assays of HUVECS cells (h), and the statistical result was showed in right column (i)
机译:A-B通过Transwell测定法测量指示治疗的蜡蜡-1(A)和ASPC-1细胞(B)的侵袭能力。秤条=50μm。 C-D通过EDU测定法测定了指示治疗蜡蜡-1(c)和ASPC-1细胞(d)的增殖能力。秤条=50μm。通过碘化丙酰染色E-G表明治疗的ASPC-1和Capan -1细胞(E)并使用流式细胞术分析,ASPC-1(F)和Capan-1(G)细胞的统计结果在右塔中显示。 H-I通过HUVECS细胞(H)的管形成测定法测量所示处理的蜡蜡和ASPC-1细胞的体外血管生成能力,统计结果显示在右柱(i)

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号