Here's an example of what's due today

Transformation and gel wet lab

Thu, Apr 29, 2027 · Week 15 · Biotechnology for Health (Biomedical Innovations)

Today's goal: Run a bacterial transformation and a gel electrophoresis to separate DNA fragments.

Learn first

What a finished product looks like

This is a model of the work you should turn in today. Use it to check your own: match the structure and the level of detail, do not copy it. Your data and wording should be your own.

Wet lab data record
Completes: Completes the wet-lab data page: transformation plate colony counts for each condition, a gel photo with labeled lanes, raw band-position measurements, and one comparison to the pre-lab prediction.

Transformation results (colony counts):

  • Cells + plasmid, antibiotic agar: 84 colonies
  • Cells + plasmid, plain agar: lawn (too many to count)
  • Cells, no plasmid, antibiotic agar: 0 colonies
  • Cells, no plasmid, plain agar: lawn

Gel setup: Lane 1 = DNA ladder, Lane 2 = uncut plasmid, Lane 3 = plasmid cut with one enzyme, Lane 4 = plasmid cut with two enzymes.

Raw band measurements (distance migrated from well):

  • Lane 3: one band at 22 mm
  • Lane 4: bands at 18 mm and 31 mm

Comparison to prediction: My pre-lab predicted no growth on the no-plasmid antibiotic plate, and I observed 0 colonies, which matches. The single-cut lane showing one band also matches the prediction that cutting a circular plasmid once gives one linear fragment.

ConditionPlasmidAntibioticColony count
AYesYes84
BYesNoLawn
CNoYes0
DNoNoLawn
Transformation colony counts: 84 colonies with plasmid on antibiotic, zero without plasmid on antibiotic, lawns on plain agar.

Also due today: Submit your lab notebook data page in the course LMS by end of class.

Check yourself

WebXam problem for today's skill

One exam-style question that uses exactly what you practiced today. Try it before you reveal the answer, then read why each choice is right or wrong.

WebXam-style domain: Bio-Molecular TechnologySelf-check skill: Relating DNA fragment size to migration distance on a gel
You load a DNA ladder and your digested samples into an agarose gel and run it. After the run, which statement about how the fragments separated is correct?

Tap an answer to see the full explanation. Nothing is recorded or graded.