| Literature DB >> 35163846 |
Sukkum Ngullie Chang1,2, Imran Khan2,3, Chang Geon Kim1, Seon Min Park1, Dong Kyu Choi4, Heejin Lee4, Buyng Su Hwang5, Sun Chul Kang2, Jae Gyu Park1.
Abstract
The author wishes to make the following correction to this paper [...].Entities:
Year: 2022 PMID: 35163846 PMCID: PMC8836268 DOI: 10.3390/ijms23031629
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923
Figure 2(A) Clonogenic assay and quantification of B16F10 cells cultured in the presence and absence of DA over 7 days, followed by crystal violet staining. (B) DA was treated to B16F10 cells for 24 h and cell cycle protein levels were detected, such as cyclin D1, CDK2, 5, 4, cyclin E, and p21. Densitometry analysis of the respective proteins was evaluated by Image J software, and results were normalized with β-actin. The data are represented as the means ± standard deviation (SD) of three independent experiments; ns—non-significant; * p < 0.05, ** p < 0.01, *** p < 0.001 vs. control, calculated through ANOVA prism.