<p>Photos with regions of interest and simultaneous single-sweep recording of two pyloric neurons, plus <i>pdn</i>. Left: first staining; right: second staining. Recordings were taken roughly 5 hours apart from one another. Staining duration was 1 hour in each case. Scale bars: 100 µm (photo) and 0.1% (optical recordings).</p
<p><b>A</b>, Representative confocal fluorescence images of sensory neurons expressing eGFP-PKC Apl ...
One of the challenges in labeling tissues for fluorescence microscopy is minimizing sample processin...
Background: Changes in neuronal excitability, synaptic efficacy and generally in cell signaling ofte...
<p>A. Original single-sweep optical recording of three different neurons (LP, PY, PD) after Di-4-ANE...
<p>A. Schematic of STNS showing experimental design for bath application of the dyes and electrophys...
<p><b>A:</b> Left, Single-sweep simultaneous optical recording of IC and the two PD neurons, along w...
<p>A. Di-4-ANEPPS was bath-applied for 24 hours and then washed out. Photos were taken every 10 minu...
<p>A: Two-photon images of individual neurons consecutively photolabeled <i>in vivo</i>. Nearby neur...
<p>Imaging was performed using the Ti-S (Nikon) (A–C) and BZ-9000 (Keyence) (D) microscopes. Neurons...
<p>(A) Experimental paradigm (sequence of loading and imaging protocols) and (B–H) a detailed illust...
<p>Dye was applied at the start of recordings. The time-lapse movie of these results can be viewed i...
<p>(<b>A–E′</b>) Images show 2-photon time-lapse recording of SR101-stainings and unstaining during ...
<p>A. There were no short-term influences on the pyloric rhythm during illumination in RH795 stained...
<p>A. Example of an extracellular recording of the triphasic pyloric rhythm on the <i>dvn</i> showin...
The two major limitations of Golgi-Cox method are that staining takes very long time and it is incon...
<p><b>A</b>, Representative confocal fluorescence images of sensory neurons expressing eGFP-PKC Apl ...
One of the challenges in labeling tissues for fluorescence microscopy is minimizing sample processin...
Background: Changes in neuronal excitability, synaptic efficacy and generally in cell signaling ofte...
<p>A. Original single-sweep optical recording of three different neurons (LP, PY, PD) after Di-4-ANE...
<p>A. Schematic of STNS showing experimental design for bath application of the dyes and electrophys...
<p><b>A:</b> Left, Single-sweep simultaneous optical recording of IC and the two PD neurons, along w...
<p>A. Di-4-ANEPPS was bath-applied for 24 hours and then washed out. Photos were taken every 10 minu...
<p>A: Two-photon images of individual neurons consecutively photolabeled <i>in vivo</i>. Nearby neur...
<p>Imaging was performed using the Ti-S (Nikon) (A–C) and BZ-9000 (Keyence) (D) microscopes. Neurons...
<p>(A) Experimental paradigm (sequence of loading and imaging protocols) and (B–H) a detailed illust...
<p>Dye was applied at the start of recordings. The time-lapse movie of these results can be viewed i...
<p>(<b>A–E′</b>) Images show 2-photon time-lapse recording of SR101-stainings and unstaining during ...
<p>A. There were no short-term influences on the pyloric rhythm during illumination in RH795 stained...
<p>A. Example of an extracellular recording of the triphasic pyloric rhythm on the <i>dvn</i> showin...
The two major limitations of Golgi-Cox method are that staining takes very long time and it is incon...
<p><b>A</b>, Representative confocal fluorescence images of sensory neurons expressing eGFP-PKC Apl ...
One of the challenges in labeling tissues for fluorescence microscopy is minimizing sample processin...
Background: Changes in neuronal excitability, synaptic efficacy and generally in cell signaling ofte...
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