Hi all
im new to this so if this has already been done and i havent searched for it sorry!
just woundering when preping plasmid DNA to analyse them with restriction enzymes why can we only use these ( in the title ) enzymes and not XHO1 or saL1 to visualise the inserts in pUC18??
thanks guys
why cut plasmid DNA with Hind111 and EcoR1?
Started by jc545staffy, Feb 15 2011 02:36 PM
1 reply to this topic













