Daniel:Notebook/ComboLock/2016-12-15
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(Started Tuesday)
RCA on Beads/Supernatant Fractions
- qPCR
- Make master mix according to following recipe
- 298.2 uL nfH2O
- 355 uL SYBR Fast
- 14.2 uL 10 uM AmpF
- Add 47 uL master mix to each well
- Add 2 uL sample and 1 uL appropriate Reverse Primer (1 uM) according to table in the following section
- qPCR Cycles
- 95C 3 min
- 95C 3 sec
- 55C 30 sec
- 72C 20 sec
- plate read
- goto b x24
- 72C 2 min
- 16C hold
- TBE Gel
- Mix 144 uL TBE, 36 uL 6x loading dye
- Aliquot 10 uL per sample/ladder lane onto parafilm
- Add 2 uL of sample or ladder to correct drop
- Load 10 uL in to well
- Run gel for 22 minutes at 250V
- Open gel and stain with 3 uL SYBR Gold for 3 minutes
- Rinse gel and image in gel doc
Sample | Condition | Fraction | Lane | AmpR Index | Sample Vol (uL) | 2X Kapa SYBR qPCR MM | 10 uM Forward Primer | 10 uM Reverse Primer | H2O | Total Volume (uL) |
Sample 1A | Sample | Supernatant | A1 | 20 | 2 | 25 | 1 | 1 | 21 | 50 |
Sample 1B | Sample | Supernatant | A2 | 20 | 2 | 25 | 1 | 1 | 21 | 50 |
Sample 2A | No Template | Supernatant | A3 | 21 | 2 | 25 | 1 | 1 | 21 | 50 |
Sample 2B | No Template | Supernatant | A4 | 21 | 2 | 25 | 1 | 1 | 21 | 50 |
Sample 3A | No C Probe | Supernatant | A5 | 22 | 2 | 25 | 1 | 1 | 21 | 50 |
Sample 3B | No C Probe | Supernatant | A6 | 22 | 2 | 25 | 1 | 1 | 21 | 50 |
Sample 1A | Sample | Beads | H1 | 23 | 2 | 25 | 1 | 1 | 21 | 50 |
Sample 1B | Sample | Beads | H2 | 23 | 2 | 25 | 1 | 1 | 21 | 50 |
Sample 2A | No Template | Beads | H3 | 24 | 2 | 25 | 1 | 1 | 21 | 50 |
Sample 2B | No Template | Beads | H4 | 24 | 2 | 25 | 1 | 1 | 21 | 50 |
Sample 3A | No C Probe | Beads | H5 | 25 | 2 | 25 | 1 | 1 | 21 | 50 |
Sample 3B | No C Probe | Beads | H6 | 25 | 2 | 25 | 1 | 1 | 21 | 50 |
NTC | qPCR Primers Only | NA | A7 | 26 | 2 | 25 | 1 | 1 | 23 | 50 |
Results
- 2016-12-15-MirrorCProbe-RCA-Supernatant.png
Gel image-supernatant RCA
- 2016-12-15-MirrorCProbe-RCA-Beads.png
Gel image-beads RCA