Team:Aachen/Notebook/Protocols/detection
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For measurement of a fluorescence response in our sensor chips we used three different methods. | For measurement of a fluorescence response in our sensor chips we used three different methods. | ||
- | '''First''', the Gel | + | '''First''', the '''Gel Doc™ XR+''' (BIO-RAD) was used, exciting with UV light for an exposure time of 1 s. |
'''Second''', we used our own device [https://2014.igem.org/Team:Aachen/Project/Measurement_Device '''WatsOn'''] with blue light for excitation (450 or 480 nm) and special filters infront of the camera for selecting the appropriate emission spectrum. You can read even more about building your own WatsOn [https://2014.igem.org/Team:Aachen/Notebook/Engineering/WatsOn here]. | '''Second''', we used our own device [https://2014.igem.org/Team:Aachen/Project/Measurement_Device '''WatsOn'''] with blue light for excitation (450 or 480 nm) and special filters infront of the camera for selecting the appropriate emission spectrum. You can read even more about building your own WatsOn [https://2014.igem.org/Team:Aachen/Notebook/Engineering/WatsOn here]. | ||
- | '''Third''', we used the [http://www.biotek.com/products/microplate_detection/synergymx_monochromator_based_multimode_microplate_reader.html Synergy Mx microplate reader] (BioTek), putting the sensor chips into the lid of a common clear well plate. GFP was measured with an excitation of 496 ± 9 nm and an emission of 516 ± 9 nm and iLOV with an excitation of 450 ± 9 nm and emission of 495 ± 9 nm. | + | '''Third''', we used the [http://www.biotek.com/products/microplate_detection/synergymx_monochromator_based_multimode_microplate_reader.html '''Synergy Mx microplate reader'''] (BioTek), putting the sensor chips into the lid of a common clear well plate. GFP was measured with an excitation of 496 ± 9 nm and an emission of 516 ± 9 nm and iLOV with an excitation of 450 ± 9 nm and emission of 495 ± 9 nm. |
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Revision as of 01:24, 17 October 2014
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