A protocol / method / schedule /procedure for extraction / isolation of both DNA and RNA from the same material typically plant leaf / leaves
(See also DNA Isolation protocol)
1) Take one medium sized leaf or half a large leaf (5 to 20 cm^2), weigh and freeze in liquid nitrogen.
2) Grind the tissue in a bleached and baked pestle and mortar with liquid nitrogen.
3) Transfer the powder produced to a l5ml Falcon blue cap tube. Add 2 ml of homogenization buffer (4 ml per g) and disperse the tissue in it.
4) Leave for 10 min at room temperature.
5) Add 2 ml of phenol/chloroform and vortex.
OR,
1) Put a small or medium sized leaf into a 4" x 6" 500 guage (thick!) plastic bag.
2) Add 2-3 ml homogenization buffer (you may need more for large leaves) to the bag.
3) Grind the leaf inside the bag using the top end of a 50 ml corex tube.
4) Pour the homogenate immediately into a 15 ml Falcon blue cap tube containing equal volume of phenol/chloroform then vortex.
5) Goto step 6
6) Spin for 10 min at 2,500 rpm in a bench centrifuge.
7) Transfer 0.7 ml of the aqueous phase to an Eppendorf tube, add 0.7 ml phenol/chloroform, vortex and spin for 5 min.
8) Transfer 0.6 ml of the aqueous phase to a fresh Eppendorf tube, add 0.6 ml phenol/chloroform, vortex and spin for 5 min.
9) Transfer 0.5 ml of the aqueous phase to a fresh Eppendorf tube, add 0.5 ml chloroform/isoamyl alcohol, vortex and spin for 5 min.
10) Add 4M LiCl to the final conc. of 2M and leave for several hrs at 4oC (better o/n). Spin for 10-15 min. RNA should be in a pellet. Remove supernatant and precipitate the DNA with ethanol.
11) Treat RNA fraction with DNase RNase-free, and the DNA fraction with RNase-free of DNase.
Notes:
Homogenization buffer:
0.1 M NaCl 2% SDS
50mM Tris-HCl pH 9.0 10 mM EDTA
(ideally DEPC treated water and everything else RNase free)
then add 0.1 mg/ml proteinase K { added fresh }
Pat Heslop-Harrison University of Leicester December 2003.
(I'm afraid I did not note the source of this protocol.)
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