Correction
Following publication of our article [1] it was noted that Figures five E and five G were the same as Figures six A and six B. Figure 1 in this correction article is the correct version of Figure six that should have been included in the original article [1]. We apologize for any inconvenience caused by this error.
Figure 1.
RT-PCR and Western blot analysis of NFκB. Total RNA and total protein were extracted from HRPC and HUVEC cultured alone or co-cultured under normoxia and hypoxia conditioned for 24 h. The expression of NFκB was measured by (A) electrophoresis of RT-PCR, (C) Western blot analysis in the HRPC and HUVEC. Figures (B, D) the band intensities corresponding to the NFκB were quantified by image analysis using a Bio-Rad scanning densitometer and Quantity One analysis software. Data were shown as ratio of NFκB densities to that of 18S RNA for RT-PCR and β-actin antibody was used to normalize Western blot for differences in loading and the transfer efficiencies. All data were expressed as mean +/- SE and results are representatives of three independent experiments.
Contributor Information
Ravindra Kumar, Email: rkumar@msm.edu.
Sandra Harris-Hooker, Email: sharris-hooker@msm.edu.
Ritesh Kumar, Email: rkumar40@gatech.edu.
Gary Sanford, Email: gsanford@msm.edu.
References
- Kumar R, Harris-Hooker S, Kumar R, Sanford G. Co-culture of Retinal and Endothelial Cells Results in the Modulation of Genes Critical to Retinal Neovascularization. Vascular Cell. 2011;3:27. doi: 10.1186/2045-824X-3-27. [DOI] [PMC free article] [PubMed] [Google Scholar]

