James K. Campbell

After talking with an outside adviser, we have realized that much of our protocol was wrong when it came to running an electrophoresis gel. We were doing a "quick run" protocol, running a high volt...

We tried again to get good results of the virus titer plaque assay. We are still getting a bit of contamination, although the growth is not bright yellow as the rest of the contamination has been. ...

There are many requirements of the iGEM competition. One of them is to create a new plasmid part on send it in for them to use and make available on their registry. For the past week, we have been ...