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Addgene inc
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Promega
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Image Search Results
Journal: PLoS ONE
Article Title: CSNK1G2 differently sensitizes tamoxifen-induced decrease in PI3K/AKT/mTOR/S6K and ERK signaling according to the estrogen receptor existence in breast cancer cells
doi: 10.1371/journal.pone.0246264
Figure Lengend Snippet: (A) Immunoblots for ER, PR, and HER2 in different human breast cancer cell lines. ER + (MCF-7 and T-47D) and ER - (MDA-MB-231) breast cancer cell lines were prepared for western blotting. The expression pattern of different hormone receptors was determined. Protein expression levels were compared to expression levels of α-tubulin; each value under the blots indicates relative protein expression levels determined by densitometric analysis, unless specifically mentioned (mean (SD); n = 4). Dots denote ER + (MCF-7 and T-47D) or ER - (MDA-MB-231) breast cancer cells treated with different concentrations of (B) TAM and (C) β-estradiol (E 2 ). Bars denote (D) ER + MCF-7, (E) ER + T-47D, and (F) ER - MDA-MB-231 breast cancer cells treated with TAM after silencing with NC or CNSK1G2 siRNA. (G) ER - MDA-MB-231 also transiently transfected with GFP-C1 or GFP-ERα plasmid DNA as well as with NC or CSNK1G1 siRNA. Twenty-four hours after transfection, cells were treated with vehicle or 1 μM TAM for 24 h. Cellular toxicity was then measured using the MTT assay (mean (SD); n = 4; * P < 0.05, ** P < 0.01, # P < 0.001 vs . each represented counterpart).
Article Snippet: pGFP-C1-ERα (GFP-ERα), a mammalian expression of ERα fused to
Techniques: Western Blot, Expressing, Transfection, Plasmid Preparation, MTT Assay
Journal: PLoS ONE
Article Title: CSNK1G2 differently sensitizes tamoxifen-induced decrease in PI3K/AKT/mTOR/S6K and ERK signaling according to the estrogen receptor existence in breast cancer cells
doi: 10.1371/journal.pone.0246264
Figure Lengend Snippet: Immunoblots for PI3K/AKT/mTOR/S6K and ERK signaling-associated proteins in (A-D) MCF-7, ( E-H) MDA-MB-231, and (I-K) GFP-ERα-overexpressed MDA-MB-231 cells. Western blotting analysis from the breast cells transfected with control siRNA ( NC ) or CSNK1G2 siRNA ( CSNK1G2 ) were performed after treatment with vehicle or 1 μM TAM for 24 h. Protein expression levels based on individual bands of phosphor were compared to expression levels of α-tubulin and/or pan (total) protein. Each value under the blots indicates relative protein expression levels determined by densitometric analysis. Data are presented as mean (SD); n = 4.
Article Snippet: pGFP-C1-ERα (GFP-ERα), a mammalian expression of ERα fused to
Techniques: Western Blot, Transfection, Control, Expressing
Journal: PLoS ONE
Article Title: CSNK1G2 differently sensitizes tamoxifen-induced decrease in PI3K/AKT/mTOR/S6K and ERK signaling according to the estrogen receptor existence in breast cancer cells
doi: 10.1371/journal.pone.0246264
Figure Lengend Snippet: (A) Cytotoxicity assay of either GFP-C1 or GFP-ERα-transfected ER - breast cancer cells. Bar denote relative percentage of % survival of transfected MDA-MB-231 cells after treatment with vehicle, 1 μM TAM, 2 μM D4476, and 1 μM TAM plus 2 μM D4476 for 24h. Cellular toxicity was measured using the MTT assay (mean (SD), n = 5; * P < 0.05, ** P < 0.01 vs . each represented counterpart). (B) Western blotting analysis from GFP-ERα-transfected ER - breast cells treated with vehicle or 2 μM D4476 together with 1 μM TAM for 24 h were performed. Immunoblots for PI3K/AKT/mTOR/S6K signaling-associated proteins in ER - MDA-MB-231 cells. Protein expression levels based on individual bands of phosphor were compared to expression levels of α-tubulin and/or pan (total) protein. Each value under the blots indicates relative protein expression levels determined by densitometric analysis (mean ± SEM, n = 4).
Article Snippet: pGFP-C1-ERα (GFP-ERα), a mammalian expression of ERα fused to
Techniques: Cytotoxicity Assay, Transfection, MTT Assay, Western Blot, Expressing