imagej software system Search Results


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GraphPad Software Inc imagej software v1.51j8
PMCA4b localization and function is impaired in the triple negative MDA-MB-231 cell line. a : Cell culture morphology analysis of the MCF-7 and MDA-MB-231 cell lines. Pictures were taken with a phase contrast microscope. Gray cell masks were made using the <t>ImageJ</t> software <t>v1.51j8</t> to emphasize the morphology of the cell cultures and cell-cell contacts. Scale bar: 30 μm. b : Subcellular localization of the PMCA4b protein in VPA-treated MCF-7 and MDA-MB-231 cells. MCF-7 cells were treated with 2 mM VPA, MDA-MB-231 cell were treated with 4 mM VPA for 4 days and immunostained with an anti-PMCA4b antibody (JA3). Images were taken by confocal microscopy. White arrows indicate PMCA4b protein in intracellular compartments. Scale bar: 30 μm. c : Relative PMCA4b expression in MCF-7 and MDA-MB-231 cells after a 4 day VPA treatment. Densitometric values of Western blots were normalized to the respective β-actin loading control levels and expressed as fold increase over the untreated controls. Bars represent mean ± SEM from two to four independent experiments. d : Ca 2+ signal measurements in VPA-treated GCaMP2-MCF-7 and GCaMP2-MDA-MB-231 cells. Cells were treated with 4 mM VPA for 4 days. Before the measurement, culture medium was replaced by HBSS supplemented with 2 mM Ca 2+ . Ca 2+ influx was triggered by 2 μM Ca 2+ ionophore A23187, and fluorescent signal of the GCaMP2 Ca 2+ sensor was followed by confocal imaging. F/F 0 values represent individual cells ( n = 14–32) from a representative experiment. e : Area under curve of the A23187-induced Ca 2+ transients. Bar graphs are means ± SEM of the individual cells ( n = 14–32). Significance between control and VPA-treated cells is denoted by *** ( P < 0.001); two-tailed unpaired t-test
Imagej Software V1.51j8, supplied by GraphPad Software Inc, 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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GraphPad Software Inc imagej plugin s-6
PMCA4b localization and function is impaired in the triple negative MDA-MB-231 cell line. a : Cell culture morphology analysis of the MCF-7 and MDA-MB-231 cell lines. Pictures were taken with a phase contrast microscope. Gray cell masks were made using the <t>ImageJ</t> software <t>v1.51j8</t> to emphasize the morphology of the cell cultures and cell-cell contacts. Scale bar: 30 μm. b : Subcellular localization of the PMCA4b protein in VPA-treated MCF-7 and MDA-MB-231 cells. MCF-7 cells were treated with 2 mM VPA, MDA-MB-231 cell were treated with 4 mM VPA for 4 days and immunostained with an anti-PMCA4b antibody (JA3). Images were taken by confocal microscopy. White arrows indicate PMCA4b protein in intracellular compartments. Scale bar: 30 μm. c : Relative PMCA4b expression in MCF-7 and MDA-MB-231 cells after a 4 day VPA treatment. Densitometric values of Western blots were normalized to the respective β-actin loading control levels and expressed as fold increase over the untreated controls. Bars represent mean ± SEM from two to four independent experiments. d : Ca 2+ signal measurements in VPA-treated GCaMP2-MCF-7 and GCaMP2-MDA-MB-231 cells. Cells were treated with 4 mM VPA for 4 days. Before the measurement, culture medium was replaced by HBSS supplemented with 2 mM Ca 2+ . Ca 2+ influx was triggered by 2 μM Ca 2+ ionophore A23187, and fluorescent signal of the GCaMP2 Ca 2+ sensor was followed by confocal imaging. F/F 0 values represent individual cells ( n = 14–32) from a representative experiment. e : Area under curve of the A23187-induced Ca 2+ transients. Bar graphs are means ± SEM of the individual cells ( n = 14–32). Significance between control and VPA-treated cells is denoted by *** ( P < 0.001); two-tailed unpaired t-test
Imagej Plugin S 6, supplied by GraphPad Software Inc, 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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Sun Microsystems Inc imagej software analysis (imagej version 1.29
PMCA4b localization and function is impaired in the triple negative MDA-MB-231 cell line. a : Cell culture morphology analysis of the MCF-7 and MDA-MB-231 cell lines. Pictures were taken with a phase contrast microscope. Gray cell masks were made using the <t>ImageJ</t> software <t>v1.51j8</t> to emphasize the morphology of the cell cultures and cell-cell contacts. Scale bar: 30 μm. b : Subcellular localization of the PMCA4b protein in VPA-treated MCF-7 and MDA-MB-231 cells. MCF-7 cells were treated with 2 mM VPA, MDA-MB-231 cell were treated with 4 mM VPA for 4 days and immunostained with an anti-PMCA4b antibody (JA3). Images were taken by confocal microscopy. White arrows indicate PMCA4b protein in intracellular compartments. Scale bar: 30 μm. c : Relative PMCA4b expression in MCF-7 and MDA-MB-231 cells after a 4 day VPA treatment. Densitometric values of Western blots were normalized to the respective β-actin loading control levels and expressed as fold increase over the untreated controls. Bars represent mean ± SEM from two to four independent experiments. d : Ca 2+ signal measurements in VPA-treated GCaMP2-MCF-7 and GCaMP2-MDA-MB-231 cells. Cells were treated with 4 mM VPA for 4 days. Before the measurement, culture medium was replaced by HBSS supplemented with 2 mM Ca 2+ . Ca 2+ influx was triggered by 2 μM Ca 2+ ionophore A23187, and fluorescent signal of the GCaMP2 Ca 2+ sensor was followed by confocal imaging. F/F 0 values represent individual cells ( n = 14–32) from a representative experiment. e : Area under curve of the A23187-induced Ca 2+ transients. Bar graphs are means ± SEM of the individual cells ( n = 14–32). Significance between control and VPA-treated cells is denoted by *** ( P < 0.001); two-tailed unpaired t-test
Imagej Software Analysis (Imagej Version 1.29, supplied by Sun Microsystems Inc, 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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Baier labs imagej software
PMCA4b localization and function is impaired in the triple negative MDA-MB-231 cell line. a : Cell culture morphology analysis of the MCF-7 and MDA-MB-231 cell lines. Pictures were taken with a phase contrast microscope. Gray cell masks were made using the <t>ImageJ</t> software <t>v1.51j8</t> to emphasize the morphology of the cell cultures and cell-cell contacts. Scale bar: 30 μm. b : Subcellular localization of the PMCA4b protein in VPA-treated MCF-7 and MDA-MB-231 cells. MCF-7 cells were treated with 2 mM VPA, MDA-MB-231 cell were treated with 4 mM VPA for 4 days and immunostained with an anti-PMCA4b antibody (JA3). Images were taken by confocal microscopy. White arrows indicate PMCA4b protein in intracellular compartments. Scale bar: 30 μm. c : Relative PMCA4b expression in MCF-7 and MDA-MB-231 cells after a 4 day VPA treatment. Densitometric values of Western blots were normalized to the respective β-actin loading control levels and expressed as fold increase over the untreated controls. Bars represent mean ± SEM from two to four independent experiments. d : Ca 2+ signal measurements in VPA-treated GCaMP2-MCF-7 and GCaMP2-MDA-MB-231 cells. Cells were treated with 4 mM VPA for 4 days. Before the measurement, culture medium was replaced by HBSS supplemented with 2 mM Ca 2+ . Ca 2+ influx was triggered by 2 μM Ca 2+ ionophore A23187, and fluorescent signal of the GCaMP2 Ca 2+ sensor was followed by confocal imaging. F/F 0 values represent individual cells ( n = 14–32) from a representative experiment. e : Area under curve of the A23187-induced Ca 2+ transients. Bar graphs are means ± SEM of the individual cells ( n = 14–32). Significance between control and VPA-treated cells is denoted by *** ( P < 0.001); two-tailed unpaired t-test
Imagej Software, supplied by Baier labs, 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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Image Search Results


PMCA4b localization and function is impaired in the triple negative MDA-MB-231 cell line. a : Cell culture morphology analysis of the MCF-7 and MDA-MB-231 cell lines. Pictures were taken with a phase contrast microscope. Gray cell masks were made using the ImageJ software v1.51j8 to emphasize the morphology of the cell cultures and cell-cell contacts. Scale bar: 30 μm. b : Subcellular localization of the PMCA4b protein in VPA-treated MCF-7 and MDA-MB-231 cells. MCF-7 cells were treated with 2 mM VPA, MDA-MB-231 cell were treated with 4 mM VPA for 4 days and immunostained with an anti-PMCA4b antibody (JA3). Images were taken by confocal microscopy. White arrows indicate PMCA4b protein in intracellular compartments. Scale bar: 30 μm. c : Relative PMCA4b expression in MCF-7 and MDA-MB-231 cells after a 4 day VPA treatment. Densitometric values of Western blots were normalized to the respective β-actin loading control levels and expressed as fold increase over the untreated controls. Bars represent mean ± SEM from two to four independent experiments. d : Ca 2+ signal measurements in VPA-treated GCaMP2-MCF-7 and GCaMP2-MDA-MB-231 cells. Cells were treated with 4 mM VPA for 4 days. Before the measurement, culture medium was replaced by HBSS supplemented with 2 mM Ca 2+ . Ca 2+ influx was triggered by 2 μM Ca 2+ ionophore A23187, and fluorescent signal of the GCaMP2 Ca 2+ sensor was followed by confocal imaging. F/F 0 values represent individual cells ( n = 14–32) from a representative experiment. e : Area under curve of the A23187-induced Ca 2+ transients. Bar graphs are means ± SEM of the individual cells ( n = 14–32). Significance between control and VPA-treated cells is denoted by *** ( P < 0.001); two-tailed unpaired t-test

Journal: BMC Cancer

Article Title: Expression of calcium pumps is differentially regulated by histone deacetylase inhibitors and estrogen receptor alpha in breast cancer cells

doi: 10.1186/s12885-018-4945-x

Figure Lengend Snippet: PMCA4b localization and function is impaired in the triple negative MDA-MB-231 cell line. a : Cell culture morphology analysis of the MCF-7 and MDA-MB-231 cell lines. Pictures were taken with a phase contrast microscope. Gray cell masks were made using the ImageJ software v1.51j8 to emphasize the morphology of the cell cultures and cell-cell contacts. Scale bar: 30 μm. b : Subcellular localization of the PMCA4b protein in VPA-treated MCF-7 and MDA-MB-231 cells. MCF-7 cells were treated with 2 mM VPA, MDA-MB-231 cell were treated with 4 mM VPA for 4 days and immunostained with an anti-PMCA4b antibody (JA3). Images were taken by confocal microscopy. White arrows indicate PMCA4b protein in intracellular compartments. Scale bar: 30 μm. c : Relative PMCA4b expression in MCF-7 and MDA-MB-231 cells after a 4 day VPA treatment. Densitometric values of Western blots were normalized to the respective β-actin loading control levels and expressed as fold increase over the untreated controls. Bars represent mean ± SEM from two to four independent experiments. d : Ca 2+ signal measurements in VPA-treated GCaMP2-MCF-7 and GCaMP2-MDA-MB-231 cells. Cells were treated with 4 mM VPA for 4 days. Before the measurement, culture medium was replaced by HBSS supplemented with 2 mM Ca 2+ . Ca 2+ influx was triggered by 2 μM Ca 2+ ionophore A23187, and fluorescent signal of the GCaMP2 Ca 2+ sensor was followed by confocal imaging. F/F 0 values represent individual cells ( n = 14–32) from a representative experiment. e : Area under curve of the A23187-induced Ca 2+ transients. Bar graphs are means ± SEM of the individual cells ( n = 14–32). Significance between control and VPA-treated cells is denoted by *** ( P < 0.001); two-tailed unpaired t-test

Article Snippet: Data were analyzed with the ImageJ software v1.51j8 and Prism 4 software v4.01 (GraphPad Software).

Techniques: Cell Culture, Microscopy, Software, Confocal Microscopy, Expressing, Western Blot, Imaging, Two Tailed Test