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Image Search Results
Journal: Advanced Science
Article Title: Targeting ATAD3A Phosphorylation Mediated by TBK1 Ameliorates Senescence‐Associated Pathologies
doi: 10.1002/advs.202404109
Figure Lengend Snippet:
Article Snippet:
Techniques: Ubiquitin Proteomics, Recombinant, Protease Inhibitor, Mutagenesis, Isolation, Staining, Membrane, One Step RT-PCR, Enzyme-linked Immunosorbent Assay, Software, Microscopy, Transmission Assay, Electron Microscopy
Journal: Frontiers in Pharmacology
Article Title: ITGAX promotes gastric cancer progression via epithelial-mesenchymal transition pathway
doi: 10.3389/fphar.2024.1536478
Figure Lengend Snippet: ITGAX overexpression promotes cell growth and migration in gastric cancer cells. (A, B) mRNA and protein levels in ITGAX-overexpressed LMSU cells, assessed by qRT-PCR and Western blotting assays. (C) Cell viability of ITGAX-overexpressed LMSU cells measured by CCK-8 assay. (D) Colony formation assay evaluating the proliferation ability of ITGAX overexpressed LMSU cells. (E, F) Cell migration ability of ITGAX-overexpressed LMSU cells assessed using the scratch assay and Transwell assay. (G) Cell invasion ability of ITGAX-overexpressed LMSU cells measured by the Transwell assay. (H) Apoptosis rate of ITGAX-overexpressed LMSU cells detected by flow cytometry. (I) EdU staining used to assess proliferation in ITGAX-overexpressed LMSU cells.
Article Snippet: Cell proliferation was detected using an
Techniques: Over Expression, Migration, Quantitative RT-PCR, Western Blot, CCK-8 Assay, Colony Assay, Wound Healing Assay, Transwell Assay, Flow Cytometry, Staining
Journal: Frontiers in Pharmacology
Article Title: ITGAX promotes gastric cancer progression via epithelial-mesenchymal transition pathway
doi: 10.3389/fphar.2024.1536478
Figure Lengend Snippet: The knockdown of ITGAX hinders gastric cancer cell growth and migration. (A, B) mRNA and protein levels in ITGAX knockdown SH-10-TC cells, assessed by qRT-PCR and Western blotting assays. (C) Cell viability of ITGAX knockdown SH-10-TC cells measured by CCK-8 assay. (D) Colony formation assay evaluating the proliferation ability of ITGAX knockdown SH-10-TC cells. (E, F) Cell migration ability of ITGAX knockdown SH-10-TC cells assessed using the scratch assay and Transwell assay. (G) Cell invasion ability of ITGAX knockdown SH-10-TC cells measured by the Transwell assay. (H) Apoptosis rate of ITGAX knockdown SH-10-TC cells detected by flow cytometry. (I) EdU staining used to assess proliferation in ITGAX knockdown SH-10-TC cells.
Article Snippet: Cell proliferation was detected using an
Techniques: Knockdown, Migration, Quantitative RT-PCR, Western Blot, CCK-8 Assay, Colony Assay, Wound Healing Assay, Transwell Assay, Flow Cytometry, Staining