--- author: Sam White toc-title: Contents toc-depth: 5 toc-location: left date: 2015-05-14 23:42:55+00:00 layout: post slug: dnase-treatment-jakes-o-lurida-ctenidia-rna-controls-from-20150507 title: DNase Treatment - Jake's O.lurida Ctenidia RNA (Controls) from 20150507 categories: - 2015 - Miscellaneous tags: - DNase - DNased RNA - NanoDrop1000 - olympia oyster - Ostrea lurida - RNA - RNA quantification - Turbo DNA-free --- Since the [O.lurida RNA I isolated on 20150507](https://robertslab.github.io/sams-notebook/posts/2015/2015-05-07-rna-isolation-jakes-o-lurida-ctenidia-control-from-20150422/) showed [residual gDNA via qPCR](https://robertslab.github.io/sams-notebook/2015/05/12/qpcr-jake-o-lurida-ctenidia-rna-control-samples-from-20150507/), I treated 5μg of RNA from each sample using the Turbo DNA-free Kit (Ambion/Life Technologies), following the "rigorous" protocol. Briefly: * 50μL reactions were carried out in 0.5mL tubes * added 1μL of DNase to each tube * incubated 30mins @ 37C * added additional 1μL of DNased * incubated 30mins @ 37C * added 0.2 vols (10.2μL) of DNase Inactivation Reagent * incubated and mixed for 2mins @ RT * transferred 50μL of supe to sterile 1.5mL snap cap tubes * spec'd on Roberts Lab NanoDrop1000 Samples were stored @ -80C in [Shellfish RNA Box #5 and Box #6](https://docs.google.com/spreadsheet/ccc?key=0AmS_90rPaQMzcHdyU1d0MDVMLWpaTWdadnJSd0M4UUE&usp=sharing). DNase reaction calcs: [20150514_Jake_Oly_control_DNase_calcs](https://docs.google.com/spreadsheets/d/1KS3tJand0vKSs6ZJk9t-hChZYmM0--RhcXiR8gDOlYo/edit?usp=sharing) Results: Google Spreadsheet: [20150514_DNased_RNA_Jake_Oly_controls_ODs](https://docs.google.com/spreadsheets/d/1vblT6zrN89k0RNi5XM1e6uaZvso1ZFCSvyIsnhhlU9E/edit?usp=sharing) ![](https://eagle.fish.washington.edu/Arabidopsis/20150514_DNased_RNA_Jake_oly_controls_ODs.JPG)(http://eagle.fish.washington.edu/Arabidopsis/20150514_DNased_RNA_Jake_oly_controls_ODs.JPG) ![](https://eagle.fish.washington.edu/Arabidopsis/20150514_DNased_RNA_Jake_oly_controls_plots_01.JPG)(http://eagle.fish.washington.edu/Arabidopsis/20150514_DNased_RNA_Jake_oly_controls_plots_01.JPG) ![](https://eagle.fish.washington.edu/Arabidopsis/20150514_DNased_RNA_Jake_oly_controls_plots_02.JPG)(http://eagle.fish.washington.edu/Arabidopsis/20150514_DNased_RNA_Jake_oly_controls_plots_02.JPG) Overall, samples look fine. Will check for residual gDNA via qPCR.