| Literature DB >> 26329470 |
Bin Li1, Ming-Zhu Huang2, Xiao-Qiang Wang3, Bang-Bao Tao1, Jun Zhong1, Xu-Hui Wang1, Wen-Chuan Zhang1, Shi-Ting Li4.
Abstract
Entities:
Year: 2015 PMID: 26329470 PMCID: PMC4556009 DOI: 10.1186/s13045-015-0199-0
Source DB: PubMed Journal: J Hematol Oncol ISSN: 1756-8722 Impact factor: 17.388
Fig. 1Suppressing of TMEM140 expression by RNAi. a TMEM140 expression level in five glioma cell lines was analyzed by RT-PCR (left) and immunoblot (middle and right). b, c The effect of TMEM140 knockdown through siRNA silencing. The cells were transfected with normal control or TMEM140-RNAi for 48 h and then subjected to RT-PCR (left) and immunoblot analysis (middle and right) of the TMEM140 expression level. The representative images for immunoblot are shown in the middle panel, and data from three independent experiments were expressed as the mean ± S.D. (right panel). Wild type: wild-type cells; normal control: scrambled siRNA transfected cells; RNAi-1, RNAi-2, and RNAi-3: TMEM140-RNAi-1, -2, and -3 transfected cells (*P < 0.05, **P < 0.01, ***P < 0.001 compared with normal control)