Dear Tobias C. Wagner

Pls. find the attached files, may help in your research , good luck

http://link.springer.com/protocol/10.1385%2F1-59259-060-8%3A53

http://www.ncbi.nlm.nih.gov/pubmed/22589122

http://www.news-medical.net/life-sciences/Northern-Blot-RNA-Blot.aspx

https://www.mskcc.org/sites/default/files/node/25002/documents/Northern%20Blot%20protocol.pdf

http://www.nature.com/protocolexchange/protocols/67#/equipment

http://www.nature.com/protocolexchange/protocols/4165#/procedure

http://www.nature.com/nprot/journal/v8/n2/full/nprot.2013.006.html

http://link.springer.com/protocol/10.1385%2F1-59259-060-8%3A53

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC298572/pdf/pnas00291-0091.pdf

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC308062/pdf/nar00033-0262.pdf

Regards

Prof. Houda Kawas

Yes 1 to 1.2% is fine. But use narrow lanes to run the sample with less voltage and less time like 60 V for 45 minutes to avoid RNA smearing...

i use 1% gel n run for 2h at 70V