2012 ha taz addgene Search Results


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Figure 1. Characterization and modulation of sub-plasma membrane mitochondria A. TIRF microscopy images of a MIN6 cell expressing mApple-Tomm20 before and during stimulation with 20 mM glucose. B. Quantification of the sub-plasma membrane density change following 15 min exposure 20 mM glucose (n=36 cells, P>0.1, paired 2-tailed Student’s t-test). C. TIRF microscopy recording of the cytosolic Ca2+ concentration <t>(GCaMP5G)</t> and cortical mitochondria (mApple-Tomm20) in a glucose-stimulated MIN6 cell.
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Figure 1. Characterization and modulation of sub-plasma membrane mitochondria A. TIRF microscopy images of a MIN6 cell expressing mApple-Tomm20 before and during stimulation with 20 mM glucose. B. Quantification of the sub-plasma membrane density change following 15 min exposure 20 mM glucose (n=36 cells, P>0.1, paired 2-tailed Student’s t-test). C. TIRF microscopy recording of the cytosolic Ca2+ concentration <t>(GCaMP5G)</t> and cortical mitochondria (mApple-Tomm20) in a glucose-stimulated MIN6 cell.
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Figure 1. Characterization and modulation of sub-plasma membrane mitochondria A. TIRF microscopy images of a MIN6 cell expressing mApple-Tomm20 before and during stimulation with 20 mM glucose. B. Quantification of the sub-plasma membrane density change following 15 min exposure 20 mM glucose (n=36 cells, P>0.1, paired 2-tailed Student’s t-test). C. TIRF microscopy recording of the cytosolic Ca2+ concentration <t>(GCaMP5G)</t> and cortical mitochondria (mApple-Tomm20) in a glucose-stimulated MIN6 cell.
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Figure 1. Characterization and modulation of sub-plasma membrane mitochondria A. TIRF microscopy images of a MIN6 cell expressing mApple-Tomm20 before and during stimulation with 20 mM glucose. B. Quantification of the sub-plasma membrane density change following 15 min exposure 20 mM glucose (n=36 cells, P>0.1, paired 2-tailed Student’s t-test). C. TIRF microscopy recording of the cytosolic Ca2+ concentration <t>(GCaMP5G)</t> and cortical mitochondria (mApple-Tomm20) in a glucose-stimulated MIN6 cell.
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Figure 1. Characterization and modulation of sub-plasma membrane mitochondria A. TIRF microscopy images of a MIN6 cell expressing mApple-Tomm20 before and during stimulation with 20 mM glucose. B. Quantification of the sub-plasma membrane density change following 15 min exposure 20 mM glucose (n=36 cells, P>0.1, paired 2-tailed Student’s t-test). C. TIRF microscopy recording of the cytosolic Ca2+ concentration <t>(GCaMP5G)</t> and cortical mitochondria (mApple-Tomm20) in a glucose-stimulated MIN6 cell.
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Figure 1. Characterization and modulation of sub-plasma membrane mitochondria A. TIRF microscopy images of a MIN6 cell expressing mApple-Tomm20 before and during stimulation with 20 mM glucose. B. Quantification of the sub-plasma membrane density change following 15 min exposure 20 mM glucose (n=36 cells, P>0.1, paired 2-tailed Student’s t-test). C. TIRF microscopy recording of the cytosolic Ca2+ concentration <t>(GCaMP5G)</t> and cortical mitochondria (mApple-Tomm20) in a glucose-stimulated MIN6 cell.
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Figure 1. Characterization and modulation of sub-plasma membrane mitochondria A. TIRF microscopy images of a MIN6 cell expressing mApple-Tomm20 before and during stimulation with 20 mM glucose. B. Quantification of the sub-plasma membrane density change following 15 min exposure 20 mM glucose (n=36 cells, P>0.1, paired 2-tailed Student’s t-test). C. TIRF microscopy recording of the cytosolic Ca2+ concentration <t>(GCaMP5G)</t> and cortical mitochondria (mApple-Tomm20) in a glucose-stimulated MIN6 cell.
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Figure 1. Characterization and modulation of sub-plasma membrane mitochondria A. TIRF microscopy images of a MIN6 cell expressing mApple-Tomm20 before and during stimulation with 20 mM glucose. B. Quantification of the sub-plasma membrane density change following 15 min exposure 20 mM glucose (n=36 cells, P>0.1, paired 2-tailed Student’s t-test). C. TIRF microscopy recording of the cytosolic Ca2+ concentration <t>(GCaMP5G)</t> and cortical mitochondria (mApple-Tomm20) in a glucose-stimulated MIN6 cell.
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Addgene inc pcdna3 1 mycbioid
Figure 1. Characterization and modulation of sub-plasma membrane mitochondria A. TIRF microscopy images of a MIN6 cell expressing mApple-Tomm20 before and during stimulation with 20 mM glucose. B. Quantification of the sub-plasma membrane density change following 15 min exposure 20 mM glucose (n=36 cells, P>0.1, paired 2-tailed Student’s t-test). C. TIRF microscopy recording of the cytosolic Ca2+ concentration <t>(GCaMP5G)</t> and cortical mitochondria (mApple-Tomm20) in a glucose-stimulated MIN6 cell.
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Image Search Results


Figure 1. Characterization and modulation of sub-plasma membrane mitochondria A. TIRF microscopy images of a MIN6 cell expressing mApple-Tomm20 before and during stimulation with 20 mM glucose. B. Quantification of the sub-plasma membrane density change following 15 min exposure 20 mM glucose (n=36 cells, P>0.1, paired 2-tailed Student’s t-test). C. TIRF microscopy recording of the cytosolic Ca2+ concentration (GCaMP5G) and cortical mitochondria (mApple-Tomm20) in a glucose-stimulated MIN6 cell.

Journal: Journal of cell science

Article Title: Cortical mitochondria regulate insulin secretion by local Ca 2+ buffering in rodent beta cells.

doi: 10.1242/jcs.228544

Figure Lengend Snippet: Figure 1. Characterization and modulation of sub-plasma membrane mitochondria A. TIRF microscopy images of a MIN6 cell expressing mApple-Tomm20 before and during stimulation with 20 mM glucose. B. Quantification of the sub-plasma membrane density change following 15 min exposure 20 mM glucose (n=36 cells, P>0.1, paired 2-tailed Student’s t-test). C. TIRF microscopy recording of the cytosolic Ca2+ concentration (GCaMP5G) and cortical mitochondria (mApple-Tomm20) in a glucose-stimulated MIN6 cell.

Article Snippet: The following plasmids were used in this study: GFP-CRY2-OCRL (Idevall-Hagren et al., 2012), CIBN-GFP-CAAX (Idevall-Hagren et al., 2012), mApple-TOMM20-N1 (Addgene plasmid #54955), R-GECO (Addgene plasmid #32444 (Zhao et al., 2011)), GCaMP5G (Addgene plasmid #31788 (Akerboom et al., 2012)), mCherry-CHUtr (Addgene plasmid #26740 (Burkel et al., 2007)), mCherry- C1aC1bPKC (Wuttke et al., 2013), iRFP-PH-PLC1 (Idevall-Hagren et al., 2012), mito- LAR-GECO (Addgene plasmid 61245 (Wu et al., 2014)), 5HT6-G-GECO (Addgene plasmid 47499 (Su et al., 2013)).

Techniques: Clinical Proteomics, Membrane, Microscopy, Expressing, Concentration Assay

Figure 3. Cortical F-actin is modulated by Ca2+. A. Kymographs from TIRF microscopy recordings of INS-1E cells expressing GCaMP5G and mCh-CHUtr following depolarization in the absence or presence of Verapamil (100 µM). B. TIRF microscopy recordings of GCaMP5G and mCh-CHUtr fluorescence changes in response to the indicated stimuli. C. Quantifications of the area under the curve for the traces in (B) (Student’s unpaired t-test: nGCAMP5G=5, PGCAMP5G=0.0241; nmCh-CHUtr=6, PmCh-CHUtr=0.02).

Journal: Journal of cell science

Article Title: Cortical mitochondria regulate insulin secretion by local Ca 2+ buffering in rodent beta cells.

doi: 10.1242/jcs.228544

Figure Lengend Snippet: Figure 3. Cortical F-actin is modulated by Ca2+. A. Kymographs from TIRF microscopy recordings of INS-1E cells expressing GCaMP5G and mCh-CHUtr following depolarization in the absence or presence of Verapamil (100 µM). B. TIRF microscopy recordings of GCaMP5G and mCh-CHUtr fluorescence changes in response to the indicated stimuli. C. Quantifications of the area under the curve for the traces in (B) (Student’s unpaired t-test: nGCAMP5G=5, PGCAMP5G=0.0241; nmCh-CHUtr=6, PmCh-CHUtr=0.02).

Article Snippet: The following plasmids were used in this study: GFP-CRY2-OCRL (Idevall-Hagren et al., 2012), CIBN-GFP-CAAX (Idevall-Hagren et al., 2012), mApple-TOMM20-N1 (Addgene plasmid #54955), R-GECO (Addgene plasmid #32444 (Zhao et al., 2011)), GCaMP5G (Addgene plasmid #31788 (Akerboom et al., 2012)), mCherry-CHUtr (Addgene plasmid #26740 (Burkel et al., 2007)), mCherry- C1aC1bPKC (Wuttke et al., 2013), iRFP-PH-PLC1 (Idevall-Hagren et al., 2012), mito- LAR-GECO (Addgene plasmid 61245 (Wu et al., 2014)), 5HT6-G-GECO (Addgene plasmid 47499 (Su et al., 2013)).

Techniques: Microscopy, Expressing, Fluorescence