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2 protocols using cleaved caspase 7 asp198

1

RPPA Analysis of Apoptosis Markers

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RPPA was performed as previously published by us [16 (link)] (more details in the Supplementary Data). The following antibodies were used: Parp-1#sc-7150 (Santa Cruz, TX, USA). Cleaved caspase-9 (Asp315) #9505, cleaved caspase-9 (Asp330) #9501, cleaved caspase-7 (Asp198) #9491 and XIAP#2042 (Cell Signaling, MA, USA).
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2

Western Blot Analysis Specifications

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Western blot analysis was performed in our previous study.5 (link) Some of the western blot results were quantified by densitometric scans using ImageJ (version 1.48p; W Rasband, National Institutes of Health; available at http://rsb.info.nih.gov/ij/) for the following Pearson’s correlation analysis. The primary antibodies of TEAD1 (sc-376113), TEAD4 (sc-134071), CTGF (L-20) (sc-14939) and Cyr-61 (sc-374129) were commercially available from Santa Cruz (Dallas, TX, USA). YAP1 (ab52771) antibody was achieved from Abcam (Cambridge, MA, USA). TEAD2 (SAB2102402) and TEAD3 (AV38278) antibodies were obtained from Sigma-Aldrich (St Louis, MO, USA). Other primary antibodies were from Cell Signaling (Danvers, MA, USA), including p21 (#2946), p27 (#2552), p-Rb (Ser807/811) (#9308), cleaved-caspase 3 (Asp175) (#9661), cleaved-caspase 7 (Asp198) (#9491), cleaved-PARP (Asp214) (#9541), cyclin D1 (#2978), cyclin D3 (#2936), CDK4 (#12790), CDK6 (#3136), c-Myc (#9402) and GAPDH (#2118). Anti-Mouse IgG-HRP (Dako, Glostrup, Denmark, 00049039, 1:30 000) and anti-Rabbit IgG-HRP (Dako, 00028856, 1:10 000) were used for secondary antibodies.
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