soft substrate 12 kpa Search Results


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CH Instruments cgas-mcherry
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BMP4-induced EMT is suppressed on compliant <t>substrates.</t> a Phase contrast images of cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels and treated with 10 nM BMP4 for up to 5 days to monitor any changes in morphology (Methods). b Immunofluorescence images of BMP4-treated OvCa429 and Panc1 cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels as described in Methods. Cells were then immunostained for E-cadherin and phalloidin/actin as indicated. Scale bars = 20 μm. c Realtime quantitative PCR of SNAI1 and SNAI2 in OvCa429, Panc1, and Py2T cells plated on soft (0.5 kPa) and rigid (8 kPa) hydrogels followed by treatment with 10 nM BMP4 (Methods). Values are normalized to their untreated control. Graphs are representative of two independent biological trials done in triplicate. *p < 0.05, **p < 0.01, ***p < 0.001
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Biomix Inc organic-matter rich substrate
BMP4-induced EMT is suppressed on compliant <t>substrates.</t> a Phase contrast images of cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels and treated with 10 nM BMP4 for up to 5 days to monitor any changes in morphology (Methods). b Immunofluorescence images of BMP4-treated OvCa429 and Panc1 cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels as described in Methods. Cells were then immunostained for E-cadherin and phalloidin/actin as indicated. Scale bars = 20 μm. c Realtime quantitative PCR of SNAI1 and SNAI2 in OvCa429, Panc1, and Py2T cells plated on soft (0.5 kPa) and rigid (8 kPa) hydrogels followed by treatment with 10 nM BMP4 (Methods). Values are normalized to their untreated control. Graphs are representative of two independent biological trials done in triplicate. *p < 0.05, **p < 0.01, ***p < 0.001
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Promega nano-glo® in vivo substrate cs320501
BMP4-induced EMT is suppressed on compliant <t>substrates.</t> a Phase contrast images of cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels and treated with 10 nM BMP4 for up to 5 days to monitor any changes in morphology (Methods). b Immunofluorescence images of BMP4-treated OvCa429 and Panc1 cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels as described in Methods. Cells were then immunostained for E-cadherin and phalloidin/actin as indicated. Scale bars = 20 μm. c Realtime quantitative PCR of SNAI1 and SNAI2 in OvCa429, Panc1, and Py2T cells plated on soft (0.5 kPa) and rigid (8 kPa) hydrogels followed by treatment with 10 nM BMP4 (Methods). Values are normalized to their untreated control. Graphs are representative of two independent biological trials done in triplicate. *p < 0.05, **p < 0.01, ***p < 0.001
Nano Glo® In Vivo Substrate Cs320501, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bio-Rad chemiluminescent substate
BMP4-induced EMT is suppressed on compliant <t>substrates.</t> a Phase contrast images of cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels and treated with 10 nM BMP4 for up to 5 days to monitor any changes in morphology (Methods). b Immunofluorescence images of BMP4-treated OvCa429 and Panc1 cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels as described in Methods. Cells were then immunostained for E-cadherin and phalloidin/actin as indicated. Scale bars = 20 μm. c Realtime quantitative PCR of SNAI1 and SNAI2 in OvCa429, Panc1, and Py2T cells plated on soft (0.5 kPa) and rigid (8 kPa) hydrogels followed by treatment with 10 nM BMP4 (Methods). Values are normalized to their untreated control. Graphs are representative of two independent biological trials done in triplicate. *p < 0.05, **p < 0.01, ***p < 0.001
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LI-COR westernsure premium chemiluminescent substract
BMP4-induced EMT is suppressed on compliant <t>substrates.</t> a Phase contrast images of cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels and treated with 10 nM BMP4 for up to 5 days to monitor any changes in morphology (Methods). b Immunofluorescence images of BMP4-treated OvCa429 and Panc1 cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels as described in Methods. Cells were then immunostained for E-cadherin and phalloidin/actin as indicated. Scale bars = 20 μm. c Realtime quantitative PCR of SNAI1 and SNAI2 in OvCa429, Panc1, and Py2T cells plated on soft (0.5 kPa) and rigid (8 kPa) hydrogels followed by treatment with 10 nM BMP4 (Methods). Values are normalized to their untreated control. Graphs are representative of two independent biological trials done in triplicate. *p < 0.05, **p < 0.01, ***p < 0.001
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Bio-Rad clarity max western ecl substarte
BMP4-induced EMT is suppressed on compliant <t>substrates.</t> a Phase contrast images of cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels and treated with 10 nM BMP4 for up to 5 days to monitor any changes in morphology (Methods). b Immunofluorescence images of BMP4-treated OvCa429 and Panc1 cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels as described in Methods. Cells were then immunostained for E-cadherin and phalloidin/actin as indicated. Scale bars = 20 μm. c Realtime quantitative PCR of SNAI1 and SNAI2 in OvCa429, Panc1, and Py2T cells plated on soft (0.5 kPa) and rigid (8 kPa) hydrogels followed by treatment with 10 nM BMP4 (Methods). Values are normalized to their untreated control. Graphs are representative of two independent biological trials done in triplicate. *p < 0.05, **p < 0.01, ***p < 0.001
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Bio-Rad chemiluminescence
BMP4-induced EMT is suppressed on compliant <t>substrates.</t> a Phase contrast images of cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels and treated with 10 nM BMP4 for up to 5 days to monitor any changes in morphology (Methods). b Immunofluorescence images of BMP4-treated OvCa429 and Panc1 cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels as described in Methods. Cells were then immunostained for E-cadherin and phalloidin/actin as indicated. Scale bars = 20 μm. c Realtime quantitative PCR of SNAI1 and SNAI2 in OvCa429, Panc1, and Py2T cells plated on soft (0.5 kPa) and rigid (8 kPa) hydrogels followed by treatment with 10 nM BMP4 (Methods). Values are normalized to their untreated control. Graphs are representative of two independent biological trials done in triplicate. *p < 0.05, **p < 0.01, ***p < 0.001
Chemiluminescence, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cell Signaling Technology Inc signalstain dab substate kit
BMP4-induced EMT is suppressed on compliant <t>substrates.</t> a Phase contrast images of cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels and treated with 10 nM BMP4 for up to 5 days to monitor any changes in morphology (Methods). b Immunofluorescence images of BMP4-treated OvCa429 and Panc1 cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels as described in Methods. Cells were then immunostained for E-cadherin and phalloidin/actin as indicated. Scale bars = 20 μm. c Realtime quantitative PCR of SNAI1 and SNAI2 in OvCa429, Panc1, and Py2T cells plated on soft (0.5 kPa) and rigid (8 kPa) hydrogels followed by treatment with 10 nM BMP4 (Methods). Values are normalized to their untreated control. Graphs are representative of two independent biological trials done in triplicate. *p < 0.05, **p < 0.01, ***p < 0.001
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Vector Laboratories dab substrate reagent from peroxidase substract kit
BMP4-induced EMT is suppressed on compliant <t>substrates.</t> a Phase contrast images of cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels and treated with 10 nM BMP4 for up to 5 days to monitor any changes in morphology (Methods). b Immunofluorescence images of BMP4-treated OvCa429 and Panc1 cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels as described in Methods. Cells were then immunostained for E-cadherin and phalloidin/actin as indicated. Scale bars = 20 μm. c Realtime quantitative PCR of SNAI1 and SNAI2 in OvCa429, Panc1, and Py2T cells plated on soft (0.5 kPa) and rigid (8 kPa) hydrogels followed by treatment with 10 nM BMP4 (Methods). Values are normalized to their untreated control. Graphs are representative of two independent biological trials done in triplicate. *p < 0.05, **p < 0.01, ***p < 0.001
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BMP4-induced EMT is suppressed on compliant <t>substrates.</t> a Phase contrast images of cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels and treated with 10 nM BMP4 for up to 5 days to monitor any changes in morphology (Methods). b Immunofluorescence images of BMP4-treated OvCa429 and Panc1 cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels as described in Methods. Cells were then immunostained for E-cadherin and phalloidin/actin as indicated. Scale bars = 20 μm. c Realtime quantitative PCR of SNAI1 and SNAI2 in OvCa429, Panc1, and Py2T cells plated on soft (0.5 kPa) and rigid (8 kPa) hydrogels followed by treatment with 10 nM BMP4 (Methods). Values are normalized to their untreated control. Graphs are representative of two independent biological trials done in triplicate. *p < 0.05, **p < 0.01, ***p < 0.001
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Image Search Results


BMP4-induced EMT is suppressed on compliant substrates. a Phase contrast images of cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels and treated with 10 nM BMP4 for up to 5 days to monitor any changes in morphology (Methods). b Immunofluorescence images of BMP4-treated OvCa429 and Panc1 cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels as described in Methods. Cells were then immunostained for E-cadherin and phalloidin/actin as indicated. Scale bars = 20 μm. c Realtime quantitative PCR of SNAI1 and SNAI2 in OvCa429, Panc1, and Py2T cells plated on soft (0.5 kPa) and rigid (8 kPa) hydrogels followed by treatment with 10 nM BMP4 (Methods). Values are normalized to their untreated control. Graphs are representative of two independent biological trials done in triplicate. *p < 0.05, **p < 0.01, ***p < 0.001

Journal: Oncogene

Article Title: Mediator kinase CDK8/CDK19 drives YAP1-dependent BMP4-induced EMT in cancer

doi: 10.1038/s41388-018-0316-y

Figure Lengend Snippet: BMP4-induced EMT is suppressed on compliant substrates. a Phase contrast images of cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels and treated with 10 nM BMP4 for up to 5 days to monitor any changes in morphology (Methods). b Immunofluorescence images of BMP4-treated OvCa429 and Panc1 cells plated on soft (0.5 kPa) and rigid (8 kPa) fibronectin-coated hydrogels as described in Methods. Cells were then immunostained for E-cadherin and phalloidin/actin as indicated. Scale bars = 20 μm. c Realtime quantitative PCR of SNAI1 and SNAI2 in OvCa429, Panc1, and Py2T cells plated on soft (0.5 kPa) and rigid (8 kPa) hydrogels followed by treatment with 10 nM BMP4 (Methods). Values are normalized to their untreated control. Graphs are representative of two independent biological trials done in triplicate. *p < 0.05, **p < 0.01, ***p < 0.001

Article Snippet: For rigidity experiments, cells were plated on 0.5 kPa (soft) or 8 kPa (rigid) substrates obtained from Matrigen Life Technologies (Brea, CA, USA), (Softslip 12-well and Softwell 6-well) that were coated with 10 μg/mL fibronectin (Cultrex® #3420–001-01) in 1 × PBS for 1 h. All cells were allowed to sit on substrates for at least 12 h before BMP4 treatment.

Techniques: Immunofluorescence, Real-time Polymerase Chain Reaction, Control