<p>A) Confocal images showing double staining for acetylcholine receptor by α-bungarotoxin (red) and mitochondria (green) using a mouse monoclonal antibody for complex VI subunit I of cytochrome c oxidase (Mitosciences, Oregon). Images represent the mean intensities of fluorescence signal across 10 z-stacked images by confocal microscopy. CP NMJs show a decreased intensity for synaptic mitochondria. B) Average mitochondrial fluorescence intensities of NMJs of CP (93.25±8.017 SEM, n = 25 NMJs) and control (156.70±12.035 SEM, n = 25 NMJs) samples. Bars represent the mean ± SEM of immunofluorescence intensity in arbitrary fluorescence units based on the signal from the mitochondrial stain at the NMJs of CP and control samples.</p
<p>(a) Fluorescent photomicrograph of THP-1 macrophages showing MMP. (b) The relative MMP level of T...
<p>A, B, C and D, are representative microphotographs of mitochondrial population under different ex...
<p>and <b>B.</b> %MTT activity as mitochondrial electron flow and UV auto-fluorescence of mitochondr...
<p>Representative images show JC-1 fluorescence in control H9c2 cells (A), H9c2 cells treated for 24...
<p>(A) Representative examples of JC1 dual color fluorescence, examined by confocal microscopy. Red ...
<p>A) Brain sections were stained with anti-synaptophysin (green), anti-ATP synthase β subunit (red)...
<p>(A) Summary graph showing persistent and transient increase in the fluorescence lifetime of Camui...
<p>(A) Differentiated human neuronal cultures were loaded with mitochondrial membrane indicator TMRM...
<p>MMP was assessed by JC-1 staining. Dual emission images (527 and 590nm) represent the signals fro...
<p>Cells were treated as labeled, stained with JC-1 dye and then observed under a fluorescence micro...
A: Representative images taken under fluorescence confocal microscope of wild type and gcn4∆ cells a...
(A) Single confocal optical sections (~0.8 μm thickness) showing overlay of LTG (green) and MTRC (re...
A: Representative images taken under fluorescence confocal microscope of wild type and gcn4∆ cells a...
<p>Mitochondrial superoxide production in hippocampal slices (400 μm) was stained employing MitoSOX ...
A: Representative images taken under fluorescence confocal microscope of wild type and gcn4∆ cells a...
<p>(a) Fluorescent photomicrograph of THP-1 macrophages showing MMP. (b) The relative MMP level of T...
<p>A, B, C and D, are representative microphotographs of mitochondrial population under different ex...
<p>and <b>B.</b> %MTT activity as mitochondrial electron flow and UV auto-fluorescence of mitochondr...
<p>Representative images show JC-1 fluorescence in control H9c2 cells (A), H9c2 cells treated for 24...
<p>(A) Representative examples of JC1 dual color fluorescence, examined by confocal microscopy. Red ...
<p>A) Brain sections were stained with anti-synaptophysin (green), anti-ATP synthase β subunit (red)...
<p>(A) Summary graph showing persistent and transient increase in the fluorescence lifetime of Camui...
<p>(A) Differentiated human neuronal cultures were loaded with mitochondrial membrane indicator TMRM...
<p>MMP was assessed by JC-1 staining. Dual emission images (527 and 590nm) represent the signals fro...
<p>Cells were treated as labeled, stained with JC-1 dye and then observed under a fluorescence micro...
A: Representative images taken under fluorescence confocal microscope of wild type and gcn4∆ cells a...
(A) Single confocal optical sections (~0.8 μm thickness) showing overlay of LTG (green) and MTRC (re...
A: Representative images taken under fluorescence confocal microscope of wild type and gcn4∆ cells a...
<p>Mitochondrial superoxide production in hippocampal slices (400 μm) was stained employing MitoSOX ...
A: Representative images taken under fluorescence confocal microscope of wild type and gcn4∆ cells a...
<p>(a) Fluorescent photomicrograph of THP-1 macrophages showing MMP. (b) The relative MMP level of T...
<p>A, B, C and D, are representative microphotographs of mitochondrial population under different ex...
<p>and <b>B.</b> %MTT activity as mitochondrial electron flow and UV auto-fluorescence of mitochondr...