Supplementary Figure 9: Primary immunoblotting data.
From: Cellular chirality arising from the self-organization of the actin cytoskeleton
(a) 10 μg samples of protein cell lysates from control siRNA- and ACTN1 siRNA-transfected cells were separated on SDS-PAGE gel and transferred to PVDF membranes. Positions of molecular weight markers are indicated to the right of each PVDF membrane. (b) Immunoblotting was performed with corresponding antibodies, anti-ACTN1, anti-ACTN4 and anti-α-tubulin, and developed using standard ECL procedure. Scans of uncropped immunoblot is shown here. Data from this immunoblot was used in Fig. 7c.
