Daniel:Notebook/HiResChrPaint/2014-2-12: Difference between revisions
Jump to navigation
Jump to search
>Djacobse No edit summary |
>Djacobse No edit summary |
||
Line 25: | Line 25: | ||
# Add 400 ul TE buffer and incubate shaking for 1 hour at 37 degC. | # Add 400 ul TE buffer and incubate shaking for 1 hour at 37 degC. | ||
# Load into nanosep tube and spin 3 minutes at 15,000 RPM. | # Load into nanosep tube and spin 3 minutes at 15,000 RPM. | ||
# Add 1 mL 100% EtOH, 40uL 3M NaOAc, and 1uL glycoblue | |||
##Incubate overnight at -80C; Continued [[Daniel:Notebook/HiResChrPaint/2014-2-13|tomorrow]] |
Revision as of 19:22, 13 February 2014
Multi-Color FISH (Started 02/08/2014)
Cot1 Labeling
The size exclusion gel didn't go great last time, so I'm going to try again and have Andrew give me a bit of coaching.
Size Exculsion Gel
To separate the fragments, I'll use a size exclusion gel. My protocol is based off Andrew's.
- For each of 4 sample pools
- Place a 0.5 ml tube inside a low binding 1.5 ml tube. Use a 20 G needle to punch a hole in the bottom of the low binding 0.5 ml tube, then UV treat.
- UV treat 400 ul TE buffer for each pool.
- Set up and UV treat a nanosep tube.
- Run samples on 5 lane PAGE gels, 250 V for 22 minutes.
- Low Mass Ladder: 10 ul dye, 2 ul low mass ladder. 38 uL 0.5x TBE
- Sample: 40 uL dye, 8 uL Cot1 DNA, 152 uL 0.5x TBE, aliquot 4 lanes of 50 uL each
- Stain with 6 uL SYBR Gold; shake for 2 minutes
- Size select with scalpel. High MW- >=400bp; Low MW- <=200bp
- Load gel fragment into 0.5 ml tube (inside 1.5 ml tube)
- Spin for 2 minutes at 12,000 RPM
- Remove and discard 0.5 ml tube.
- Add 400 ul TE buffer and incubate shaking for 1 hour at 37 degC.
- Load into nanosep tube and spin 3 minutes at 15,000 RPM.
- Add 1 mL 100% EtOH, 40uL 3M NaOAc, and 1uL glycoblue
- Incubate overnight at -80C; Continued tomorrow