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Edvard Grødem, Kieran Sweeney, Megan N. McClean 2020. OptoPlate Calibration protocol. protocols.io https://dx.doi.org/10.17504/protocols.io.bivmke46Copy Citation Copied
URL: https://dx.doi.org/DOI:10.17504/protocols.io.bivmke46
Authors: Edvard Grødem, Kieran Sweeney, Megan N. McClean
Summary: Optogenetic systems use light to precisely control and investigate cellular processes. Until recently, there had been few instruments available for applying controlled light doses to cultures of cells. The optoPlate, a programmable array of 192 LEDs, was developed to meet this need. However, LED performance varies and without calibration there are substantial brightness differences between LEDs on an optoPlate. Here we present a method for calibrating an optoPlate that uses a programmable microscope stage and optical power meter to automatically measure all 192 LEDs of an optoPlate. The resulting brightness measurements are used to calculate calibration values that tune the electrical current supplied to each optoPlate LED to reduce brightness variation in optogenetic experiments.
Affiliations: Department of Biomedical Engineering, University of Wisconsin-Madison, Madison, WI USA, Department of Biomedical Engineering, University of Wisconsin-Madison, Madison, WI USA, Department of Biomedical Engineering, University of Wisconsin-Madison, Madison, WI USA
Version: 1
Publication Date: 2020
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