There was an error in Biology Open (2019) 8, bio038554 (doi:10.1242/bio.038554).
The 1BLCTL PY-Enolase panel in Fig. 1C was inadvertently a duplicate of the 1ALCTL panel. The corrected and original panels are shown below; both the online full text and PDF versions of the paper have been corrected.
Stable transfected Arg isoforms and their kinase activity. (C) Tyrosine kinase assay in vitro of the indicated Arg isoforms transfected in Hek cell line. In C and D, the cellular lysates were IP with antibody against Flag. Kinase reaction of IP proteins was performed in presence of ATP and enolase. IB with antibodies against PY and enolase.
Stable transfected Arg isoforms and their kinase activity. (C) Tyrosine kinase assay in vitro of the indicated Arg isoforms transfected in Hek cell line. In C and D, the cellular lysates were IP with antibody against Flag. Kinase reaction of IP proteins was performed in presence of ATP and enolase. IB with antibodies against PY and enolase.
(original panel). Stable transfected Arg isoforms and their kinase activity. (C) Tyrosine kinase assay in vitro of the indicated Arg isoforms transfected in Hek cell line. In C and D, the cellular lysates were IP with antibody against Flag. Kinase reaction of IP proteins was performed in presence of ATP and enolase. IB with antibodies against PY and enolase.
(original panel). Stable transfected Arg isoforms and their kinase activity. (C) Tyrosine kinase assay in vitro of the indicated Arg isoforms transfected in Hek cell line. In C and D, the cellular lysates were IP with antibody against Flag. Kinase reaction of IP proteins was performed in presence of ATP and enolase. IB with antibodies against PY and enolase.
The authors apologise to readers for this error, which does not impact the results or conclusions of the paper.