Anyone know if i can use Qiagen's qiaquick purification to purify ssRNA?
I need to remove the EDTA from my DNasing step
will phenol purification also work?
RNA Purification
Started by dreww, Sep 02 2009 06:57 PM
3 replies to this topic
#1
Posted 02 September 2009 - 06:57 PM
#2
Posted 03 September 2009 - 12:24 AM
You can use any kit for RNA purification, but generally for obtaining high quality RNA without loosing much RNA, we use LiCl (lithium chloride) method to clean the RNA. So let me give the procedure:
1 volume of 7,5 M lithium chloride
1 volume of DNAse treated RNA sample
1 volume of nuclease free water
(so final concentration of lithium chloride will be 2,5 molar)
mix them, put -20 for at least 1 hour, overnight is always better, centrifuge at 15,300 rpm (or max speed on microcentrifuge) for 15-20 min at +4 C, discard the supernetant, add 1 ml of 70% EtoH (it should be -20 chilled), centrifuge at max speed for 15-20 min., discard the supernatant, dry the pellet, resuspend with nuclease free water.
it seems a bit long but to be in safe side this is the best way
good luck
1 volume of 7,5 M lithium chloride
1 volume of DNAse treated RNA sample
1 volume of nuclease free water
(so final concentration of lithium chloride will be 2,5 molar)
mix them, put -20 for at least 1 hour, overnight is always better, centrifuge at 15,300 rpm (or max speed on microcentrifuge) for 15-20 min at +4 C, discard the supernetant, add 1 ml of 70% EtoH (it should be -20 chilled), centrifuge at max speed for 15-20 min., discard the supernatant, dry the pellet, resuspend with nuclease free water.
it seems a bit long but to be in safe side this is the best way
good luck
Edited by microRNA, 03 September 2009 - 12:26 AM.
#3
Posted 03 September 2009 - 12:25 AM
that s all
Edited by microRNA, 03 September 2009 - 12:27 AM.
#4
Posted 03 September 2009 - 01:05 PM
Thanks a lot!!! Glad someone could help me out here.














