Haynes Lab:Notebook/Synthetic Biology and Bioinformatics for Predictable Control of Therapeutic Gene2/2013/01/07
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(Autocreate 2013/01/07 Entry for Haynes_Lab:Notebook/Synthetic_Biology_and_Bioinformatics_for_Predictable_Control_of_Therapeutic_Gene2) |
Current revision (14:47, 11 January 2013) (view source) (→Entry title) |
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| - | == | + | ==RNeasy Mini Kit== |
| - | + | #Add 100μL of chloroform to each tube | |
| + | #Shake vigorously for 20 sec and let sit for 2 min | ||
| + | #Centrifuge in cold room for 15 min @ 12,000G | ||
| + | #Pipet off clear phase from organic phase into new tube (warning: do not get pink stuff in the tube!) | ||
| + | #Add 70% ethanol into tube (1:1 ratio) | ||
| + | #Transfer to collection tube (we have K562 1, K562 2, SK-N-SH 1, and SK-N-SH 2) | ||
| + | #Spin tubes at top speed for 30 sec | ||
| + | #Discard collected liquid and add 700μL of RW1 Buffer | ||
| + | #Spin tubes at top speed for 30 sec | ||
| + | #Put collection vial in a fresh collector tube and discard of the old one | ||
| + | #Add 500μL of RBE Buffer | ||
| + | #Spin tubes at top speed for 30 sec then discard of the liquid waste | ||
| + | #Repeat the above two steps again | ||
| + | #Discard of the waste and spin again | ||
| + | #Transfer liquid to a fresh tube and add 30mL of RNase-Free H20 | ||
| + | #Let tubes sit for 1 min | ||
| + | #Spin tubes for 1 min | ||
| + | #Store at -80°C | ||
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RNeasy Mini Kit
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