sw1222 Search Results


99
CancerTools Org sw1222
Sw1222, supplied by CancerTools Org, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sw1222/SW1222/custom%40152434%4010%2E1021%2Fbc500499h
Average 99 stars, based on 1 article reviews
sw1222 - by Bioz Stars, 2026-10
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90
European Collection of Authenticated Cell Cultures sw1222 crc cells
TGFβ does not modify the effects of EVs either in EGF-dependent or in EGF-independent 3D models. (A) The percentage of active caspase-3+ cells in CRC patient-derived organoid lines in the presence or absence of AREG, control, or TGFβ-treated NCF-derived EVs. (B) The effect of NCF-derived EVs on CRC organoids. NCFs were pre-treated with TGFβ (TGFβ EV) or they were cultured untreated (Ctr EV) before collecting EVs. (C) Detecting AREG on EVs isolated from control (Ctr EV) or TGFβ-treated NCFs (TGFβ EV) and bound to latex beads (flow cytometry). (D,E) The percentage of KI67+ cells in <t>SW1222</t> cell-derived colonies in the presence of the indicated treatments. Representative confocal microscopic images (D) and their quantification (E) . EVs were isolated from control or TGFβ-treated (4 days) NCF cultures. Kruskal–Wallis and Dunn’s multiple comparison tests were used (A,B,E) . Confocal microscopic images were quantified from three experiments for (A,B,E) . Scale bars: 50 μm (D) . * p < 0.05, ** p < 0.01, *** p < 0.005.
Sw1222 Crc Cells, supplied by European Collection of Authenticated Cell Cultures, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sw1222/sw1222+crc+cells/pmc07381355-32-0-7
Average 90 stars, based on 1 article reviews
sw1222 crc cells - by Bioz Stars, 2026-10
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90
Corning Life Sciences sw1222 cells
TGFβ does not modify the effects of EVs either in EGF-dependent or in EGF-independent 3D models. (A) The percentage of active caspase-3+ cells in CRC patient-derived organoid lines in the presence or absence of AREG, control, or TGFβ-treated NCF-derived EVs. (B) The effect of NCF-derived EVs on CRC organoids. NCFs were pre-treated with TGFβ (TGFβ EV) or they were cultured untreated (Ctr EV) before collecting EVs. (C) Detecting AREG on EVs isolated from control (Ctr EV) or TGFβ-treated NCFs (TGFβ EV) and bound to latex beads (flow cytometry). (D,E) The percentage of KI67+ cells in <t>SW1222</t> cell-derived colonies in the presence of the indicated treatments. Representative confocal microscopic images (D) and their quantification (E) . EVs were isolated from control or TGFβ-treated (4 days) NCF cultures. Kruskal–Wallis and Dunn’s multiple comparison tests were used (A,B,E) . Confocal microscopic images were quantified from three experiments for (A,B,E) . Scale bars: 50 μm (D) . * p < 0.05, ** p < 0.01, *** p < 0.005.
Sw1222 Cells, supplied by Corning Life Sciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sw1222/sw1222+cells/pm37052759-105-18-31
Average 90 stars, based on 1 article reviews
sw1222 cells - by Bioz Stars, 2026-10
90/100 stars
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Image Search Results


TGFβ does not modify the effects of EVs either in EGF-dependent or in EGF-independent 3D models. (A) The percentage of active caspase-3+ cells in CRC patient-derived organoid lines in the presence or absence of AREG, control, or TGFβ-treated NCF-derived EVs. (B) The effect of NCF-derived EVs on CRC organoids. NCFs were pre-treated with TGFβ (TGFβ EV) or they were cultured untreated (Ctr EV) before collecting EVs. (C) Detecting AREG on EVs isolated from control (Ctr EV) or TGFβ-treated NCFs (TGFβ EV) and bound to latex beads (flow cytometry). (D,E) The percentage of KI67+ cells in SW1222 cell-derived colonies in the presence of the indicated treatments. Representative confocal microscopic images (D) and their quantification (E) . EVs were isolated from control or TGFβ-treated (4 days) NCF cultures. Kruskal–Wallis and Dunn’s multiple comparison tests were used (A,B,E) . Confocal microscopic images were quantified from three experiments for (A,B,E) . Scale bars: 50 μm (D) . * p < 0.05, ** p < 0.01, *** p < 0.005.

Journal: Frontiers in Cell and Developmental Biology

Article Title: Fibroblast-Derived Extracellular Vesicles Induce Colorectal Cancer Progression by Transmitting Amphiregulin

doi: 10.3389/fcell.2020.00558

Figure Lengend Snippet: TGFβ does not modify the effects of EVs either in EGF-dependent or in EGF-independent 3D models. (A) The percentage of active caspase-3+ cells in CRC patient-derived organoid lines in the presence or absence of AREG, control, or TGFβ-treated NCF-derived EVs. (B) The effect of NCF-derived EVs on CRC organoids. NCFs were pre-treated with TGFβ (TGFβ EV) or they were cultured untreated (Ctr EV) before collecting EVs. (C) Detecting AREG on EVs isolated from control (Ctr EV) or TGFβ-treated NCFs (TGFβ EV) and bound to latex beads (flow cytometry). (D,E) The percentage of KI67+ cells in SW1222 cell-derived colonies in the presence of the indicated treatments. Representative confocal microscopic images (D) and their quantification (E) . EVs were isolated from control or TGFβ-treated (4 days) NCF cultures. Kruskal–Wallis and Dunn’s multiple comparison tests were used (A,B,E) . Confocal microscopic images were quantified from three experiments for (A,B,E) . Scale bars: 50 μm (D) . * p < 0.05, ** p < 0.01, *** p < 0.005.

Article Snippet: SW1222 CRC cells were obtained from ECACC (European Collection of Authenticated Cell Cultures) and they were cultured in DMEM containing 4,500 g/L glucose (Gibco), 10% FBS (Biosera), glutamine (Sigma), and 1× penicillin/streptomycin (Gibco).

Techniques: Derivative Assay, Control, Cell Culture, Isolation, Flow Cytometry, Comparison