The main regulators of Arp2/3 activity appear to be N‐WASP and the other members of the Scar/WAVE family of proteins. We show here that after EGF stimulation, N‐WASP is recruited to the nucleation zone of the dynamic leading edge compartment of carcinoma cells, with maximal recruitment of N‐WASP within 1 min after EGF stimulation. The timing of N‐WASP recruitment mirrors the timing of barbed‐end formation at the leading edge. To determine the cellular activation of N‐WASP after EGF stimulation, we made a conformation‐sensitive antibody (CSA) against the CRIB domain of N‐WASP that is predicted to recognize N‐WASP in its open, active conformation, but not in its closed, inactive conformation. The ability of CSA to detect only active N‐WASP was demonstrated by in vitro experiments using immunoprecipitation of active N‐WASP from EGF‐stimulated cells and Cdc42 activation of N‐WASP activity. In cell staining experiments, N‐WASP is maximally accessible to CSA 40 sec after EGF stimulation and this activated N‐WASP is in the nucleation zone. These results indicate that active N‐WASP is present at the leading edge of lamellipods, an unexpected finding given its reported involvement in filopod formation. This work establishes the feasibility of using antibodies directed against specific conformations or epitopes with changing accessibilities as a window on the status and localization of activity. Cell Motil. Cytoskeleton 59:141–152, 2004. © 2004 Wiley‐Liss, Inc.