Difference between revisions of "Team:UMaryland/Results"

Revision as of 03:59, 18 September 2015

Considerations

PCR of Hok-Sok Construct

Amplification of the Hok-Sok cassette is difficult due to the high inherent secondary structure in the construct. Hok ssDNA is capable of naturally folding into a stable secondary structure, resulting in early terminations and other side products. We recommend that a reaction buffer suitable for difficult templates be used, such as Phusion GC buffer + added DMSO.

Measuring OD of RFP Cultures

Due to the close proximity of the emission wavelength of RFP (584 nm) and the classical absorbance wavelength for measuring cell density (600 nm), it is difficult to accurately determine the cell density of cultures that are expressing RFP. Given more time to calibrate our testing measurements, we would either have used an alternative wavelength for measuring OD (>600 nm), used a hemocytometer as an alternate counting method, or switched to GFP as an alternative fluorescent marker whose emission wavelength differs from 600 nm by a greater amount.

Project Results

Here you can describe the results of your project and your future plans.

What should this page contain?

Clearly and objectively describe the results of your work.

Future plans for the project

Considerations for replicating the experiments

Project Achievements

You can also include a list of bullet points (and links) of the successes and failures you have had over your summer. It is a quick reference page for the judges to see what you achieved during your summer.

A list of linked bullet points of the successful results during your project

A list of linked bullet points of the unsuccessful results during your project. This is about being scientifically honest. If you worked on an area for a long time with no success, tell us so we know where you put your effort.

Inspiration

See how other teams presented their results.

@@ Line 92: / Line 92: @@
 <h1 align="center">Plating Tests</h1>
-<h2>Negative Control (No Pressure)</h2>
+<h2><b>Negative Control (No Pressure)</b></h2>
 <p><img src = "https://static.igem.org/mediawiki/2015/5/5d/UMDnegcontrolplate2.png"></p>
 <p style = "font-size:18px">Figure 1. Negative control was K1783002 (constitutive unstable RFP) grown in media without chloramphenicol. After 2-3 days, plates demonstrate fewer than 10 colonies per plate, indicating that resistance is now only minimally present in the culture.</p>
 <br>
-<h2>Chloramphenicol Pressure Only</h2>
+<h2><b>Chloramphenicol Pressure Only</b></h2>
 <p><img src = "https://static.igem.org/mediawiki/2015/e/ea/UMDchlorplate.png"></p>
 <p style = "font-size:18px">Figure 2. K1783002 (constitutive unstable RFP) grown in media with chloramphenicol. Colonies persist through several days of plating, indicating that antibiotic resistance was maintained throughout the test. A loss of colony redness was also observed over time, which is discussed later.</p>

Difference between revisions of "Team:UMaryland/Results"

Revision as of 03:59, 18 September 2015

Plating Tests

Negative Control (No Pressure)

Chloramphenicol Pressure Only

Growth Curve

Future Plans

Considerations

Project Results

What should this page contain?

Project Achievements

Inspiration