Team:Aachen/Notebook/Protocols/Analytical methods
From 2014.igem.org
(→Analytical Methods) |
(→Analytical Methods) |
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# apply onto agarose gel together with a marker | # apply onto agarose gel together with a marker | ||
# run at 120 mA for 40 minutes for a full gel | # run at 120 mA for 40 minutes for a full gel | ||
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== SDS-PAGE == | == SDS-PAGE == | ||
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== Bradford Assay == | == Bradford Assay == | ||
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This assay is used for the determination of the protein concentration in a sample. | This assay is used for the determination of the protein concentration in a sample. | ||
* mix the Bradford solution with ddH{{sub|2}}O in a ratio of 1:4 | * mix the Bradford solution with ddH{{sub|2}}O in a ratio of 1:4 | ||
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== Measurement of Fluorescence == | == Measurement of Fluorescence == | ||
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The measurement of fluorescence was performed using the Synergy Mx (BioTek) microplate reader and the Gen5 software. | The measurement of fluorescence was performed using the Synergy Mx (BioTek) microplate reader and the Gen5 software. | ||
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== Measurement of Optical Density == | == Measurement of Optical Density == | ||
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Depending on the number of samples, two different devices were used for measurement of optical density, the Unico Spectrophotometer 1201 (Fisher Bioblock Scientific) and the Synergy Mx (BioTek) microplate reader. | Depending on the number of samples, two different devices were used for measurement of optical density, the Unico Spectrophotometer 1201 (Fisher Bioblock Scientific) and the Synergy Mx (BioTek) microplate reader. | ||
Revision as of 02:19, 17 October 2014
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