View source for Golden Gate Assembly for Bio113

==Starting with Boiled then Cooled Oligos==
# You should have already used the [http://gcat.davidson.edu/iGem10/index.html Oligator] to design your oligos for your dsDNA control element. <br>
# You should have already calculated how to dilute your boiled and cooled oligos from 5 µM to 40 nM. <br>

==Protocol Details for GGA==

# You will be given two tubes. One tube will be labeled "X" for eXperimental DNA, the other "N" for the negative control that contains plasmid only. Put your initials on the tubes and return the tubes to ice. These tubes will already contain 9 µL of the GGA Mixture.
# Add 1 µL '''diluted''' oligos cooled overnight to the tube labeled '''X''' for the experimental DNA.
# Add 1 µL '''water''' to the tube labeled '''N''' for the negative control"

'''GGA mixture contains:'''<br>
* 1 µL (40 nM) plasmid containing your receiving plasmid (pClone)<br> 
* 6 µL dH<sub>2</sub>O <br> 
* 1 µL 10X Promega Ligase Buffer<br> 
* 0.5 µL Bsa I high fidelity (HF) restriction enzyme<br> 
* <u>0.5 µL T4 DNA ligase from Promega</u><br> 
* 9 µL final volume <br> <br> 

Turn on the thermocycler. Put '''both''' of your tubes into the machine. <br> 
Program it for the following cylces: <br> 
* 20 cycles of 37C for 1.5 minute and 16C for 1.5 minute <br> 
* 22C holding temperature <br> 
* heated lid on

This DNA ligation is ready for transformation. <br> <br> 

You can increase the number of cycles to 30 if you want to increase yield. However, we have gotten good success with as few as 5 cycles.


This protocols was developed at MWSU by Dr. Todd Eckdahl, and modified at Davidson College by Annie Wacker and Malcolm Campbell.