<p dir="ltr">Scaffold files following mass spectrometry of proteins isolated on streptavidin beads following proximity biotinylation. This was done using (1 file) full-length APEX2 fused to the N-terminus of SRSF1 and (1 file) split-APEX, with complementary portions of APEX2 fused to the N-terminus of SRSF1 and to the N-terminus of helicases involved in pre-mRNA splicing. Experiments were done in triplicate.</p>
Funding
Strategic Longer and Larger Grant: Frontier Bioscience from the Biotechnology and Biological Sciences Research Council, BBSRC (How do RNA-binding proteins control splice site selection? BB/T000627/1)