DNA agarose gel electrophoresis
Posted 27 March 2010 - 08:49 AM
lane 1 - 1kb DNA ladder
my sample are..
lane 14 - isolated DNA plasmid
1.how many band should appear? 2 or 3? which band belong to which form of plasmid?
2. the upper band means high genome contaminate? what is this means? how cause this happen?
3. the smearing at the bottom means contaminated by protein and RNA? how?
lane 15 - PCR product
lane 18 - uncut plasmid DNA (pBR322)
how many band should appear? isn't same with the isolated plasmid?
lane 19 - cut plasmid DNA (pBR322)
lane 20 - no added topoisomerase DNA
why the band with supercoil DNA is not same with the isolated DNA?
isn't got many type of supercoil DNA?
lane 21-25 - added topoisomerase DNA with 2min, 5min, 10min, 20min and 30min.
what cause no increase in the intensity with the time ?
last question is ..
izit different form of DNA(relax, linear , supercoil) will have differ molecular weight?
Posted 28 March 2010 - 03:52 PM
Posted 28 March 2010 - 04:18 PM
di203 - Throw your thoughts about this gel our way and we'll help to guide you.
Posted 30 March 2010 - 07:00 PM