Summary
- Gel #2 was tried with fresh APS 10% (previous was 1 month old)
- Still large blur was seen during and after running the gel.
- When checking pH of the stacking gel a pH of 7.15 was found instead of 6.8
- This will prevent the stacking function and would explain the blur seen while running
- New stacking buffer was prepared
- 18.9 g TRIS
- 150 mL dH2O
- pH 6.8
- added to 250 mL with dH2O
- Gel #3 was prepared
- All other gels stored at 4 °C were discarded
- To prevent more wasting of samples only marker and loading buffer (4x) was used
- seemed to run owkay after also running buffer was renewed
- Immunotreatment of blot #2 was performed as described yesterday
Materials & Methods
Materials
Method
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