Selected article for: "culture plate and tissue culture"

Author: Li, Lv; Dai, Hong-Juan; Ye, Mao; Wang, Shu-Ling; Xiao, Xiao-Juan; Zheng, Jie; Chen, Hui-Yong; Luo, Yu-hao; Liu, Jing
Title: Lycorine induces cell-cycle arrest in the G0/G1 phase in K562 cells via HDAC inhibition
  • Document date: 2012_11_23
  • ID: 13amcxh2_26
    Snippet: Cell viability and cytotoxicity were measured with 2-(2-methoxy-4-nitrophenyl)-3-(4-nitrophenyl)-5-(2,4disulfophenyl)-2H tetrazolium monosodium salt (CCK-8) assay as described previously. Briefly, exponentially growing K562 cells treated with various concentrations of lycorine (1.25, 2.5, or 5.0 μM) or without lycorine were cultivated at 1.25 × 10 4 cells/well in a 96-well tissue culture plate (BioCoat) at a total volume of 100 μL per well. Af.....
    Document: Cell viability and cytotoxicity were measured with 2-(2-methoxy-4-nitrophenyl)-3-(4-nitrophenyl)-5-(2,4disulfophenyl)-2H tetrazolium monosodium salt (CCK-8) assay as described previously. Briefly, exponentially growing K562 cells treated with various concentrations of lycorine (1.25, 2.5, or 5.0 μM) or without lycorine were cultivated at 1.25 × 10 4 cells/well in a 96-well tissue culture plate (BioCoat) at a total volume of 100 μL per well. After cells were incubated for 24 and 48 h, 10 μL of CCK-8 solution (Beyotime) was added to each well and incubation of cells was performed for another 4 h at 37°C. The relative cell viability was determined by scanning with an ELISA reader with a 450 nm filter and calculated by CCK-8 assay.

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