I am continuously getting some precipitates in pockets in gel electrophoresis. I have tried with incubating the samples at around 40°C for 1hr and also I have tried with low concentration of agar. I am still getting this problem.
Paul Rutland
what samples are you running in what amounts and dissolved in what? What type and concentration of gel and gel running buffer are you using?
Can you post a picture please?
1 votes
1 thanks
Sudeep Jain
If you are running DNA then purify it, there may be higher amount of protein present in your sample.
0 votes
0 thanks
Faryal Ahmed
Hello Narayan
1st you must mention here what sample are you running.Sample amount and storage conditions.
2nd check the gel preparation method
3rd again make sure your sample preparation method.
0 votes
0 thanks
- Badges
- Science method
More Narayan Parajuli's questions See All
Similar questions and discussions