Freimoser:Protocols:FastYeastTransformation
From OpenWetWare
(Difference between revisions)
m |
|||
| Line 29: | Line 29: | ||
*Plasmid: 100 ng - 1 μg | *Plasmid: 100 ng - 1 μg | ||
*carrier DNA: salmon/herring sperm DNA in H2O, 2mg/ml stock, 500 µl aliquots, heat-inactivated at 95°C for 5-6 min and put on ice before use (has to be done once). | *carrier DNA: salmon/herring sperm DNA in H2O, 2mg/ml stock, 500 µl aliquots, heat-inactivated at 95°C for 5-6 min and put on ice before use (has to be done once). | ||
| - | *50% poly-ethylen-glycol (PEG) (MW | + | *50% poly-ethylen-glycol (PEG) (MW 3'350) solution, filter-sterilized |
*1M Li-Acetate, autoclaved | *1M Li-Acetate, autoclaved | ||
Revision as of 05:29, 22 December 2006
Protocol: Fast yeast transformation
- Add 50 μl carrier DNA to a 1.5 ml tube.
- scrap cells from plate and add to the carrier DNA.
- Add in the following order:
- 1-2 μl DNA-plasmid (up to 30-50 μl)
- 240 vl PEG (50%)
- 36 μl Li-Ac (1M)
- resuspend with blue tip
- incubate at 30°C or RT at least 30 min
- heat shock: 45°C, 15 min (or 42°C for 20 min)
- spin down, resuspend in 100μl H2O and plate everything on corresponding medium
Material:
- Plasmid: 100 ng - 1 μg
- carrier DNA: salmon/herring sperm DNA in H2O, 2mg/ml stock, 500 µl aliquots, heat-inactivated at 95°C for 5-6 min and put on ice before use (has to be done once).
- 50% poly-ethylen-glycol (PEG) (MW 3'350) solution, filter-sterilized
- 1M Li-Acetate, autoclaved
Reference
- Gietz D, St Jean A, Woods RA, and Schiestl RH. . pmid:1561104.
