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. 2021 Mar 3;4(5):e201900332. doi: 10.26508/lsa.201900332

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© 2021 Afanasyeva et al.

This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/).

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Figure S6. — (A) Immunolabelling of TRIO and TIAM1 in IMR-32, SK-N-BE(2)c, and KELLY grown on (collagenIV/laminin/fibronectin)-coated plastic. Scale bar 20 μm. (B) Subcellular localisation of kalirin-STYV, Golgi apparatus and γ-tubulin (left) in IMR-32 cells. Scale bar 10 μm. For superimposed images (right), centrosome-specific (centrin-2), and Golgi apparatus signals were colored green. Scale bar 5 μm. (C) Heterogeneity of kalirin-SP and kalirin-STYV subcellular localisation in IMR-32 and SK-N-BE(2)c. Scale bar 20 μm. (D) WB analysis of TIAM1, TRIO, and kalirin in IMR-32 cells after 48 h of SOX11 RNAi. (E) Migration fronts of NB-S-124 stained by kalirin-STYV and kalirin-SP. Scale bar 10 μm.