This can be attributed to both technical and procedural errors that occurred during the experiment. Early on in the series of labs, we had to spool the E. coli DNA, which had us wipe off excess ethanol off of the spooled DNA on paper towels. In doing so, it is plausible that some DNA could have been wiped off along with the ethanol. No DNA here means that there would be no DNA on the gel. A remedy for this problem would be to have a different technique to remove the ethanol. Moreover, the agarose gel that we made had a low concentration of 0.7%; therefore, it hindered the movement of any smaller strands of DNA. Lower concentrations of agarose gel are better for allowing large strands of DNA to move through. Additionally, experiments that run only one trial are less trustworthy, since results differ between trials. Adding more trials could allow for a higher chance of getting results that you want; in this case, getting DNA on the gel. Some possible extra trials could be growing more colonies of E. coli, or making multiple gels to collect a variety of