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2 protocols using phospho fak y397

1

Immunoblotting Antibody Validation Protocol

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Primary antibodies used for immunoblotting were as follows: total and cleaved forms of PARP and caspase-3, phospho-KIT Y719, phospho-AKT S473, AKT, ABCG2, phospho-FGFR Y653/654 (Cell Signaling, Danvers, MA, USA), FAK, phospho-FAK Y397 (BD Biosciences, Franklin Lakes, NJ, USA), KIT (DakoCytomation), phospho-Met Tyr1230/1234/1235 (R&D Systems, Minneapolis, MN, USA), Axl, FGFR2 (Sigma), c-Met, MDR, MRP-1 and actin (Santa Cruz Biotechnology, Dallas, TX, USA). The HRP-conjugated secondary antibodies for Western blotting were purchased from Santa Cruz Biotechnology.
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2

Immunoblot Analysis of Cell Adhesion Proteins

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Immunoblot assays were performed as described previously (Oh et al., 2001.). The primary antibodies used were as follows: RECK (5B11D12)6 (link), E-cadherin (610181, BD Biosciences), N-cadherin (610920, BD Biosciences), FN (610077, BD Biosciences), α-tubulin (CP06, Calbiochem), vimentin (V5255, Sigma), phospho-FAK (Y397) (611722, BD Biosciences), FAK (sc-557, Santa Cruz), integrin α5 (610633, BD Biosciences), and integrin β1 (610467, BD Biosciences).
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