2. How will the bands we see determine the amount of DNA we got?
1. Today we will be looking at our gels for the DNA Quantitation lab, where did the DNA for the gels come from?
2. How will the bands we see determine the amount of DNA we got?
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1. Calculate the amount of agarose needed to make a 40 ml solution of 1% TAE agarose solution.
2. Describe how to make 40 ml molten 1% TAE agarose, that is ready to pour into a gel casting tray. (Assume TAE was already diluted to 1x ) 1. Why is ampicillin added to media?
2. Have the E. coli in our pGLO lab been genetically engineered to be resistant to an antibiotic? How? |
Mrs. HusselsteinBiotechnology II Warm-Up questions. Please write your answers in the Warm-Up document provided weekly on Google Classroom. Archives
December 2018
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