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©2013 Baishideng Publishing Group Co.
World J Gastroenterol. Jun 7, 2013; 19(21): 3226-3240
Published online Jun 7, 2013. doi: 10.3748/wjg.v19.i21.3226
Published online Jun 7, 2013. doi: 10.3748/wjg.v19.i21.3226
Figure 8 Identification of the effectiveness of lysine-acetylated antibodies enriching acetylated proteins.
Line 1: 20 μg total protein from AGS cells unexposed to trichostatin A (TSA); Line 2: 20 μg total protein from AGS cells exposed to 0.5 μmol/L TSA; Line 3: 20 μg flow-through protein from AGS cells unexposed to TSA, which was incubated with an antibody gel column; Line 4: 20 μg flow-through protein from AGS cells exposed to 0.5 μmol/L TSA, which was incubated with an antibody gel column; Line 5: 100 ng enriched protein from AGS cells unexposed to TSA, which was incubated with an antibody gel column; and Line 6: 100 ng enriched protein from AGS cells exposed to 0.5 μmol/L TSA, which was incubated with an antibody gel column.
- Citation: Wang YG, Wang N, Li GM, Fang WL, Wei J, Ma JL, Wang T, Shi M. Mechanisms of trichostatin A inhibiting AGS proliferation and identification of lysine-acetylated proteins. World J Gastroenterol 2013; 19(21): 3226-3240
- URL: https://www.wjgnet.com/1007-9327/full/v19/i21/3226.htm
- DOI: https://dx.doi.org/10.3748/wjg.v19.i21.3226