Once the plasmid was inserted into the bacteria, it was able to fluoresce. These are the four different dishes of bacteria.

This photo shows that under UV light, the only colonies that fluoresced were the pGLO which had arabinose in their environment.

Thanks for dropping by samcareybiology! Take a look around and grab the RSS feed. Mdash; Leave a comment. Plate with -pGLO and just LB. In this lab, we attempted to complete a transformation of a gene into a bacteria. We used plasmids, small rings of DNA, to insert a new gene into.

Where it is copied into a form of RNA by the RNA polymerase. This process goes through 3 stages starting with. Where the RNA polymerase binds to the DNA on a certain location. Where the copying is complete and the RNA can then proceed.

On May 6, 2012. On April 5, 2012. On February 17, 2012. N order to seperate the DNA, we had to first dissolve the cell membrane. Once the detergent had dissolved the nuclear and cellular membranes, the DNA was released. Because the DNA is less dense than water, it floats above the water. In alcohol, DNA forms into clusters and strands, which is what we could see in our test tube. On February 10, 2012. On November 29, 2011. On November 16, 2011.

Potted Plants at the End of the Rainbow. Be sure to check out the videos at the bottom of the Procedure page! November 30, 2011.

3 We found that adding the pGLO DNA to the bacteria made them ampicillin resistant. My infographic is about the relationship between the GDP per capita of a country and the number of deaths in a country.

In this lab, we genetically transformed. Final Project for my Chapter 7 Lab. For this lab, my group decided to investigate if different types of plants perform photosynthesis at different rates. Here is a link to our online poster. How does the hydra eat? November 7, 2011.

E Coli and pGLO Lab. On May 7, 2012. It is these proteins that are responsible for phenotypical traits.

On May 6, 2012. Smoking and Lung Cancer Infographic.