| Literature DB >> 29867067 |
Won-Kyung Cho1, Prasanna Weeratunga2, Byeong-Hoon Lee3, Jun-Seol Park4, Chul-Joong Kim5, Jin Yeul Ma6, Jong-Soo Lee7.
Abstract
The authors wish to make the following change to their paper [1].[...].Entities:
Year: 2018 PMID: 29867067 PMCID: PMC6024753 DOI: 10.3390/v10060304
Source DB: PubMed Journal: Viruses ISSN: 1999-4915 Impact factor: 5.048
Figure 3Induction of cytokines and the phosphorylation of the signal molecules by Epimedium koreanum Nakai in vitro. (A) RAW264.7; and (B) HEK293T cells were treated with DMEM containing 10% FBS alone, with 1000 unit/mL recombinant mouse or human IFN-β, or with 1.0 μg/mL Epimedium koreanum Nakai (EKN). This was incubated at 37 °C with 5% CO2. Supernatant from each group was harvested at 0, 12 and 24 hpt and clarified by centrifugation at 2500× g for 10 min at 4 °C. Clarified supernatants were dispensed into the murine IFN-β and IL-6 as well as human IL-6 and IFN-β capture antibody-coated ELISA plate to measure cytokine secretion. The test was performed in duplicate for IFN-β and human IL-6 and in triplicate for other cytokines. The data shows the representative means ± SD of each murine cytokine measured over time; (C) for the determination of Type I IFN-related or NF-κB related protein phosphorylation, cells were harvested at 0, 8, 12 and 24 hpt with LPS or Epimedium koreanum Nakai (EKN) and washed with phosphate-buffered saline (PBS), before being subjected to immunoblot analysis. The samples were separated by SDS-PAGE, transferred onto a PVDF membranes and were probed with the target protein antibodies (anti-IRF3/anti-phopho-IRF3, anti-p65/anti-phopho-p65, anti-STAT1/anti-phopho-STAT1, anti-TBK1/anti-phopho-TBK1, anti-p38/anti-phopho-p38, anti-ERK/anti-phopho-ERK, anti-β-actin) before being visualized with the enhanced chemiluminescence detection system (ECL-GE healthcare) using a ImageQuant LAS 4000 mini (GE healthcare, North Richland Hills, TX, USA).