JCB logo
Avanti Polar Lipids, Inc.
  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents

This Article
Right arrow Abstract
Right arrow Full Text
Services
Right arrow Email this article
Right arrow Alert me to new content in the JCB
Citing Articles
Right arrow Citing Articles via CrossRef

Index of Online Supplemental Material for
J. Cell Biol. 10.1083/jcb.200209019
Lampugnani et al.

Figure S1 Accessibility of VEGFR-2 in VEC-null and -positive cells.

Figure S2 Confluent VEC-null and -positive endothelial cells were stimulated with VEGF (80 ng/ml) for 10 and 160 min.

Figure S3 Inhibition of phosphotyrosine phosphatases with pervanadate releases the inhibition of VEGFR-2 tyrosine phosphorylation in VEC-positive endothelial cells.

Figure S4 Immunofluorescence microscopy of VEC-positive cells transfected with DEP-1 wt, DEP-1 C/S, DEP-1 siRNA, and scramble (scr) siRNA.

Figure S5 DEP-1 C/S point mutated in the cysteine residue 1239 essential for tyrosine phosphatase activity increases VEGFR-2 phosphorylation at tyr 996 and 951.

Figure S6 Tyrosine phosphorylation of VEGFR-2 in sparse and confluent VEC-positive cells transfected with DEP-1 wt or DEP-1 C/S.





This Article
Right arrow Abstract
Right arrow Full Text
Services
Right arrow Email this article
Right arrow Alert me to new content in the JCB
Citing Articles
Right arrow Citing Articles via CrossRef


  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents