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INTEGRIN AFFINITY AND FOCAL ADHESION DYNAMICS • MILLON-FR É MILLON ET AL. 441 Downloa<strong>de</strong>d from jcb.rupress.org on March 30, 2009
tel-00435843, version 1 - 24 Nov 2009 Figure S1: <strong>ICAP</strong>-1 loss induces no changes in the distribution of β3 integrin containing FA and in the expression of adhesion proteins. A. Confocal images of Icap-1 +/+ and Icap-1 -/- MEF cells. Cells were cultured overnight on 1µg/ml FN and processed for immunostaining to visualize β3 integrin and vinculin. B. <strong>ICAP</strong>-1 and FA proteins expression in Icap-1 +/+ and Icap-1 -/- MEF cells. An equal amount of protein from cell lysates in radioimmunoprecipitation assay was subjected to Western blotting analysis using either anti-<strong>ICAP</strong>-1 pAb, anti-talin, anti-vinculin or anti-paxillin mAb. The same membrane has been blotted with anti-actin mAb to control loading. C. Cell surface analysis of β1- and β3- integrin expression on Icap-1 +/+ and Icap-1 -/- MEF cells estimated by flow cytom<strong>et</strong>ry. (left) Icap-1 +/+ (b<strong>la</strong>ck line and red line) or Icap-1 -/- cells (dashed line and blue line) were stained with control antibody (b<strong>la</strong>ck line) or with anti-β1 MB1.2 mAb. (right) Icap-1 +/+ (b<strong>la</strong>ck and blue lines) or Icap-1 -/- (dashed and red lines) cells were stained with control antibody (b<strong>la</strong>ck line) or with anti-β3 rat mAb. Bar, 20µm.
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