Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2022 May 12;33(6):tp1. doi: 10.1091/mbc.E21-10-0506

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© 2022 Hobson and Aaron. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology.

This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial-Share Alike 4.0 International Creative Commons License.

PMC Copyright notice

FIGURE 2: — Multi-instrument microscopy experiments examine FA dynamics and architecture in hPSCs. (A) Representative SD confocal image depicting paxillin-positive FAs located at the cell edge (green) and cell interior (magenta). Selected time points of 0 min (green), 50 min (cyan), and 100 min (magenta) are shown for both edge and center FAs. White regions indicate highly stable FAs. (B) Corresponding images of the inset square region shown in A. (C–F). Lateral (top) and axial (bottom) projections of iPALM images of (C) Eos-tagged integrin β5, (D) paxillin, (E) Eos-tagged actin, and (F) Eos-tagged α-actinin. Color scale in each bottom panel represents axial position as noted. Scale bar = 1 µm. (G) Average (and standard deviation) axial positions of hPSC cornerstone FA components as determined from iPALM images. Images are reproduced with permission from Stubb, Guzmán, et al. (2019).