- Email: [email protected]
Corrigendum to: “Proteomic investigation of embryonic rat heart-derived H9c2 cell line sheds new light on the molecular phenotype of the popular cell model” [Exp. Cell Res. 339 2 (2015) 174–186]
Experimental Cell Research 343 (2016) 267
Contents lists available at ScienceDirect
Experimental Cell Research journal homepage: www.elsevier.com/locate/yexcr
Corrigendum
Corrigendum to: “Proteomic investigation of embryonic rat heart-derived H9c2 cell line sheds new light on the molecular phenotype of the popular cell model” [Exp. Cell Res. 339 2 (2015) 174–186] Juraj Lenčo a, Olga Lenčová-Popelová b, Marek Link a, Anna Jirkovská c, Vojtěch Tambor d, Eliška Potůčková c, Jiří Stulík a, Tomáš Šimůnek c, Martin Štěrba b,n a
Department of Molecular Pathology and Biology, Faculty of Military Health Sciences, University of Defense, 50001 Hradec Králové, CzechRepublic Department of Pharmacology, Faculty of Medicine in Hradec Králové, Charles University in Prague, 50038 Hradec Králové, CzechRepublic c Department of Biochemical Sciences, Faculty of Pharmacy in Hradec Králové, Charles University in Prague, 50005 Hradec Králové, CzechRepublic d Biomedical Research Center, University Hospital Hradec Králové, 50005 Hradec Králové, CzechRepublic b
The authors regret that wrong version of Fig. 4 with incorrect representative western blot image for DNA Topoisomerase 2-beta was included in to the publication. The correct version of the Fig. 4 is provided herein. The text of the article and the figure legends are referring to the appropriate version of the Fig. 4 and thus they are valid as published. The authors would like to apologize for this error and any inconvenience caused.
Fig. 4. Western blot analysis of selected muscle-specific and non-specific proteins in H9c2 cells, isolated neonatal ventricular cardiomyocytes and adult rat LV myocardium. nH9c2: non-proliferating cells cultured 24 h in serum-free media, pH9c2: proliferating cells cultured in serum-containing media (10% FBS), nVCM: neonatal ventricular cardiomyocytes, adult left ventricular myocardium. Protein load per line was 10 μg.
n
DOI of original article: http://dx.doi.org/10.1016/j.yexcr.2015.10.020 Corresponding author.
http://dx.doi.org/10.1016/j.yexcr.2016.02.007 0014-4827/& 2016 Elsevier Inc. All rights reserved.
Contents lists available at ScienceDirect
Experimental Cell Research journal homepage: www.elsevier.com/locate/yexcr
Corrigendum
Corrigendum to: “Proteomic investigation of embryonic rat heart-derived H9c2 cell line sheds new light on the molecular phenotype of the popular cell model” [Exp. Cell Res. 339 2 (2015) 174–186] Juraj Lenčo a, Olga Lenčová-Popelová b, Marek Link a, Anna Jirkovská c, Vojtěch Tambor d, Eliška Potůčková c, Jiří Stulík a, Tomáš Šimůnek c, Martin Štěrba b,n a
Department of Molecular Pathology and Biology, Faculty of Military Health Sciences, University of Defense, 50001 Hradec Králové, CzechRepublic Department of Pharmacology, Faculty of Medicine in Hradec Králové, Charles University in Prague, 50038 Hradec Králové, CzechRepublic c Department of Biochemical Sciences, Faculty of Pharmacy in Hradec Králové, Charles University in Prague, 50005 Hradec Králové, CzechRepublic d Biomedical Research Center, University Hospital Hradec Králové, 50005 Hradec Králové, CzechRepublic b
The authors regret that wrong version of Fig. 4 with incorrect representative western blot image for DNA Topoisomerase 2-beta was included in to the publication. The correct version of the Fig. 4 is provided herein. The text of the article and the figure legends are referring to the appropriate version of the Fig. 4 and thus they are valid as published. The authors would like to apologize for this error and any inconvenience caused.
Fig. 4. Western blot analysis of selected muscle-specific and non-specific proteins in H9c2 cells, isolated neonatal ventricular cardiomyocytes and adult rat LV myocardium. nH9c2: non-proliferating cells cultured 24 h in serum-free media, pH9c2: proliferating cells cultured in serum-containing media (10% FBS), nVCM: neonatal ventricular cardiomyocytes, adult left ventricular myocardium. Protein load per line was 10 μg.
n
DOI of original article: http://dx.doi.org/10.1016/j.yexcr.2015.10.020 Corresponding author.
http://dx.doi.org/10.1016/j.yexcr.2016.02.007 0014-4827/& 2016 Elsevier Inc. All rights reserved.