Literature DB >> 22449250

Correction: Co-culture of Retinal and Endothelial Cells Results in the Modulation of Genes Critical to Retinal Neovascularization.

Ravindra Kumar1, Sandra Harris-Hooker, Ritesh Kumar, Gary Sanford.   

Abstract

Entities:  

Year:  2012        PMID: 22449250      PMCID: PMC3350405          DOI: 10.1186/2045-824X-4-6

Source DB:  PubMed          Journal:  Vasc Cell        ISSN: 2045-824X


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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.

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.
  1 in total

1.  Co-culture of Retinal and Endothelial Cells Results in the Modulation of Genes Critical to Retinal Neovascularization.

Authors:  Ravindra Kumar; Sandra Harris-Hooker; Ritesh Kumar; Gary Sanford
Journal:  Vasc Cell       Date:  2011-11-23
  1 in total
  1 in total

1.  Triptolide represses oral cancer cell proliferation, invasion, migration, and angiogenesis in co-inoculation with U937 cells.

Authors:  Cheng-Yu Yang; Chih-Kung Lin; Gu-Jiun Lin; Cheng-Chih Hsieh; Shing-Hwa Huang; Kuo-Hsing Ma; Yi-Shing Shieh; Huey-Kang Sytwu; Yuan-Wu Chen
Journal:  Clin Oral Investig       Date:  2016-04-13       Impact factor: 3.573

  1 in total

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