Maho's Quick Yeast Transformation (revised)

From Powers Lab UC Davis

1. Put patch of cells from plate into 1.5 ml microfuge tube containing 100µl LiOAc mix.

2. Boil 10µl of salmon sperm DNA 5 minutes.

3. Add salmon sperm DNA and plasmid DNA (about 10 µl of Qiagen miniprep) to cells.

4. Add 700µl of PEG solution to cells and mix; incubate at 30°C for 1 hr.

5. Heat shock 5 minutes at 42°C.

6. Spin down cells (8000 rpm, 5 min).

7. Resuspend in 100µl H2O and plate on selective plates.


LiOAc Mix

1 ml 10X TE
1 ml 1M LiOAc
8ml sterile H2O

PEG Mix

8 ml 50% PEG 3000
1 ml 10X TE
1 ml 1M LiOAc