by Sathya » Sun Oct 14, 2012 9:19 am
I have prepared RNAs using multiple methods and analyzed by Northerns, RNAseq, PCR, making full length libraries. Ambion kits, standard good old Guanidinium method and trizol were used depending on the amount of tissues I am using for specific experiments. For my downstream applications (see above), these methods did not make any difference. I must admit that for preparing the full length libraries I used Guanidinium and Trizol methods. I would go with Trizol method. Probably we should process the samples immediately after isolating from the animals.