Haynes Lab:Notebook/CRISPR Editing/2015/07/05: Difference between revisions
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Rene M Davis (talk | contribs) (Autocreate 2015/07/05 Entry for Haynes_Lab:Notebook/CRISPR_Editing) |
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== | ==07/05/2015== | ||
Transfected siRNAs EZH2 and SUZ12 into gal4-EEDs with and without dox<br> | |||
Cells plated yesterday looked good. | |||
:Cells plated at 30% were at about 80% | |||
:Cells plated at 10% and 20% were at about 50%<br> | |||
Transfected 2 wells for each siRNA and each cell type | |||
<br><br> | |||
Resuspended duplex siRNAs with 100ul of unopened, RNase-free water for final concentration 20uM. Used RNase-away to reduce risk of degradation. | |||
<br> | |||
''Mix optimem and siRNA'' | |||
:11ul siRNA + 176ul Optimem in 1.5mL tube<br> | |||
''Mix oligofectamine and optimem | |||
:14.25ul oligofectamine + 57ul optimem | |||
:let stand for 10 minutes<br> | |||
''Mix DNA and oligofectamine'' | |||
:add 33ul oligofectamine to tubes with DNA | |||
:let stand for 30 minutes | |||
''While complexes form, prep cells'' | |||
:Removed media | |||
:Wash in 100ul PBS | |||
:Aspirate PBS | |||
:Add 200ul of plain DMEM<br> | |||
''Add complexes to cells''<br> | |||
:Add 50ul complexes dropwise to each well | |||
<br> | |||
{| {{table}} | |||
| align="center" style="background:#f0f0f0;"|'''Component''' | |||
| align="center" style="background:#f0f0f0;"|'''Final vol / well''' | |||
|- | |||
| 20uM siRNA duplex||2.5 | |||
|- | |||
| Optimem||46 | |||
|- | |||
| Oligofectamine||1.5 | |||
|- | |||
| Total||50 | |||
|} | |||
<br> | |||
After 4 hours, add 125ul DMEM + 3x serum to each well. | |||
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Revision as of 15:29, 5 July 2015
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07/05/2015Transfected siRNAs EZH2 and SUZ12 into gal4-EEDs with and without dox
Transfected 2 wells for each siRNA and each cell type
Mix oligofectamine and optimem
Mix DNA and oligofectamine
While complexes form, prep cells
Add complexes to cells
|