The Mac
@TheMac
10 June, 08:37
An elegant way to precisely target 👉🏻optogenetic probes👈🏻👉🏻 to individual neurons is to use single-cell 👉🏻electroporation42,44 (Fig. 3). This involves using 👉🏻2-photon microscopy👈🏻 to target a plasmid-filled patch pipette to 👉🏻individual neurons in vivo and using 👉🏻electrical pulses33,34 to deliver the 👉🏻plasmid to the cell 👈🏻👉🏻under visual control.👉🏻 Neurons can be targeted this way based on their somatodendritic morphology👉🏻 (using ‘shadowimaging’33), 👉🏻their genetic identity👉🏻 (using GFP expression as a marker) 👉🏻or their functional properties (such as tuned responses to sensory stimuli) for subsequent 👉🏻optogenetic activation34.👈🏻
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10 June, 08:44
In response The Mac to his Publication
Yup.
People are now row-bots.
People are now row-bots.
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The Mac
@TheMac
10 June, 09:28
In response Photon 333 to her Publication
Hey Photon,
👉🏻momentarily👈🏻
👉🏻momentarily👈🏻
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10 June, 09:39
In response The Mac to his Publication
And, of course, that makes uninformed abuse okay.🙄
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Only people mentioned by TheMac in this post can reply
The Mac
@TheMac
11 June, 12:12
In response The Mac to his Publication
Two-photon excitation microscopy (TPEF or 2PEF) is a fluorescence imaging technique that allows imaging of living tissue up to about one millimeter in thickness. Unlike traditional fluorescence microscopy, in which the excitation wavelength is shorter than the emission wavelength, two-photon excitation requires simultaneous excitation by two photons with longer wavelength than the emitted light.
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The Mac
@TheMac
11 June, 12:13
In response The Mac to his Publication
A fluorophore (or fluorochrome, similarly to a chromophore) is a fluorescent chemical compound that can re-emit light upon light excitation. Fluorophores typically contain several combined aromatic groups, or planar or cyclic molecules with several π bonds.
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