cane lv | cane activated neuron ensemble cane lv CANE is a new technology for capturing activated (Fos+) neuronal ensembles. CANE tags Fos+neurons with high specificity, temporal precision, and efficiency. Hypothalamic neurons . Born for high-altitude Himalayan climbing, the Explorer arrived in 1953, the same year as the Submariner and the Turn-O-Graph. To say it was a major year for Rolex, and for watches more broadly, would be an understatement. It shaped the watch company that Rolex would become, the sport segment as we know it, and the watch-collecting .
0 · cane technology
1 · cane neuronal ensemble
2 · cane activated neuron ensemble
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cane technology
CANE is a new technology for capturing activated (Fos+) neuronal ensembles. CANE tags Fos+neurons with high specificity, temporal precision, and efficiency. Hypothalamic neurons .
CANE-LV-Cre achieves permanent labeling of previously activated neurons . CANE-captured social fear-activated neurons (SFNs) in the ventromedial hypothalamus (VMHvl) bi .
We developed a technology (capturing activated neuronal ensembles [CANE]) to label, manipulate, and transsynaptically trace neural circuits that are transiently activated in .
CANE is a new technology for capturing activated (Fos+) neuronal ensembles. CANE tags Fos+neurons with high specificity, temporal precision, and efficiency. Hypothalamic neurons .CANE-LV-Cre achieves permanent labeling of previously activated neurons . CANE-captured social fear-activated neurons (SFNs) in the ventromedial hypothalamus (VMHvl) bi . CANE uses Fos TVA knock-in mice and engineered viruses (CANE-lentivirus (CANE-LV)) to express desired transgenes in Fos + cells.
In a two-bout experimental paradigm, CANE was used to capture PB cl neurons activated by drinking condensed milk through co-injection of CANE-LV-Cre and AAV-flex-GFP .By contrast, EnvAM21 pseudotyped lentivirus (CANE-LV) specifically infected VMHvl neurons only after social fear experienced in FosTVA mice. White dash circles indicate the structure of .
Using a novel activity-dependent technology called CANE developed in our lab, we identified and selectively labeled noxious stimuli-activated PB L neurons, and performed comprehensive .IEG promoters drive transient effector expression in recently activated neurons. Transgenic animals using IEG promoters to drive fluo-rescent reporters (Figure 1a) enabled researchers to .Plasmid CANE-LV envelope from Dr. Fan Wang's lab contains the insert CANE-LV envelope and is published in Neuron. 2016 Nov 23;92(4):739-753. doi: 10.1016/j.neuron.2016.10.015. Epub . To use the CANE method, painful stimulus is applied to Fos dsTVA mice, followed by 60–90 min of waiting in the homecage (single-housed), followed by stereotaxic surgery to .
We developed a technology (capturing activated neuronal ensembles [CANE]) to label, manipulate, and transsynaptically trace neural circuits that are transiently activated in .CANE is a new technology for capturing activated (Fos+) neuronal ensembles. CANE tags Fos+neurons with high specificity, temporal precision, and efficiency. Hypothalamic neurons .CANE-LV-Cre achieves permanent labeling of previously activated neurons . CANE-captured social fear-activated neurons (SFNs) in the ventromedial hypothalamus (VMHvl) bi . CANE uses Fos TVA knock-in mice and engineered viruses (CANE-lentivirus (CANE-LV)) to express desired transgenes in Fos + cells.
cane neuronal ensemble
cane activated neuron ensemble
In a two-bout experimental paradigm, CANE was used to capture PB cl neurons activated by drinking condensed milk through co-injection of CANE-LV-Cre and AAV-flex-GFP .By contrast, EnvAM21 pseudotyped lentivirus (CANE-LV) specifically infected VMHvl neurons only after social fear experienced in FosTVA mice. White dash circles indicate the structure of .Using a novel activity-dependent technology called CANE developed in our lab, we identified and selectively labeled noxious stimuli-activated PB L neurons, and performed comprehensive .
IEG promoters drive transient effector expression in recently activated neurons. Transgenic animals using IEG promoters to drive fluo-rescent reporters (Figure 1a) enabled researchers to .
Plasmid CANE-LV envelope from Dr. Fan Wang's lab contains the insert CANE-LV envelope and is published in Neuron. 2016 Nov 23;92(4):739-753. doi: 10.1016/j.neuron.2016.10.015. Epub .
$14K+
cane lv|cane activated neuron ensemble
