DPNI-caged-GABA
Chemical Name: 1-(4-Aminobutanoyl)-4-[1,3-bis(dihydroxyphosphoryloxy)propan-2-yloxy]-7-nitroindoline
Purity: ≥98%
Biological Activity
Nitroindoline-caged GABA (Cat.No. 0344) with similar photochemical properties to MNI-glutamate (Cat. No. 1490); for example, the same quantum yield (0.085). Highly water soluble; exhibits fast photorelease that is efficient at near-UV and 405 nm wavelengths.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Additional Information
Background References
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Synthesis and photochemistry of photolabile derivatives of gamma-aminobutyric acid for chemical kinetic investigations of the gamma-aminobutyric acid receptor in the millisecond time region.
Wieboldt et al.
Biochemistry, 1994;33:1526 -
Laser photolysis of DPNI-GABA, a tool for investigating the properties and distribution of GABA receptors and for silencing neurons in situ.
Trigo et al.
J.Neurosci.Meths., 2009;181:159 -
Presynaptic miniature GABAergic currents in developing interneurons.
Trigo
Neuron, 2010;66:235
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Citations for DPNI-caged-GABA
The citations listed below are publications that use Tocris products. Selected citations for DPNI-caged-GABA include:
2 Citations: Showing 1 - 2
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KCC2-Mediated Cl- Extrusion Modulates Spontaneous Hippocampal Network Events in Perinatal Rats and Mice.
Authors: Spoljaric Et al.
Cell Rep 2019;26:1073
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Disruption of centrifugal inhibition to olfactory bulb granule cells impairs olfactory discrimination.
Authors: Nunez-Parra Et al.
PLoS One 2013;110:14777
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