E. Coli Lab

Words: 591
Pages: 3

The purpose of the series of E. coli labs was to isolate its DNA and analyze it through gel electrophoresis. Although I was unable to isolate any E. Coli DNA, my partner was able to; thus, any comparisons use her DNA. Furthermore, we ran our salmon sperm DNA on the gel as a visualizer for large amounts of DNA on the gel. Also, there was a pGLO plasmid as a positive control, and a ladder, to compare base pairs on the bands of DNA. On the gel, I can see three things of importance. First, the salmon sperm DNA shows up in bright, large streaks on the gel. Next, the band of JM109 DNA (the strand of E. Coli used in the experiment) was high up, but light. Finally, the only visible band of E. coli is roughly aligned with the top band of the ladder. For gel electrophoresis, brighter bands equates to a higher …show more content…
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