Ran qPCR on DNased RNA from earlier today to assess whether there was any residual gDNA after the DNase treatment with Oly_Actin_F/R primers (SR IDs: 1505, 1504).
Used 1μL from all templates.
All samples were run in duplicate.
Positive control was HL1 O.lurida DNA isolated by Jake on 20150323.
Cycling params:
95C – 2.5mins
40 cycles of:
95C – 10s
60C – 20s
Melt curve
Master mix calcs are here: 201500806_qPCR_Oly_DNased_RNA
qPCR Plate Layout: 20150806_qPCR_plate_Jake_Oly_DNased_RNA
RESULTS:
qPCR Data File (Opticon):
qPCR Report (Google Spreadsheet): - 20150806_qPCR_Report_Jake_Oly_DNased_RNA
Positive control comes up around cycle ~21.
No amplification in the no template controls.
Two wells of the DNased RNA samples exhibit amplification (E3, F6), however the corresponding respective replicate does not. Will proceed with reverse transcription.
Amplification Plots
Positive Controls
Melt Curves
Positive Controls (HL1)
DNased RNA Samples
Follow the green and red lines with the vertical bars. The different colors reflect that those are two different samples. Additionally, their respective replicates do not exhibit amplification.
