Team:Alberta/Project/Transformation

From 2009.igem.org

(Difference between revisions)
(New page: {{:Team:Alberta/Template3}} <html> <head> <style type="text/css"> .b1f, .b2f, .b3f, .b4f{font-size:1px; overflow:hidden; display:block;} .b1f {height:1px; background:#e1e1e1; margin:0 5px;...)
 
(One intermediate revision not shown)
Line 53: Line 53:
</ul>
</ul>
-
<p>==Notes==
+
<h2>Notes</h2>
<ul><li>The competent cells we have made up are XL10-Gold – if we need to transfer them to DH5alpha at a later date we can retransform the final BioBricks
<ul><li>The competent cells we have made up are XL10-Gold – if we need to transfer them to DH5alpha at a later date we can retransform the final BioBricks
<li>Can try 200 ul of cells instead of 100 ul to attempt to increase efficiency of transformation.
<li>Can try 200 ul of cells instead of 100 ul to attempt to increase efficiency of transformation.
</ul>
</ul>
-
</p>
 
<b class="b4f"></b><b class="b3f"></b><b class="b2f"></b><b class="b1f"></b>
<b class="b4f"></b><b class="b3f"></b><b class="b2f"></b><b class="b1f"></b>

Latest revision as of 22:18, 12 October 2009

University of Alberta - BioBytes










































































































Transformations

What you will need:

  • “Competent” XL10 Gold cells (100 uL per transformation)
  • 1 uL of plasmid you want to transform
  • 1 mL of LB (non-contaminated) per transformation
  • Plate with correct antibiotics (3 per transformation)

Procedure:

  • Obtain XL10 Gold* cells from the –70 C freezer (GXXX, grey Nunc freezer, 2nd shelf from bottom) and allow to thaw on ice. Aliquots are about 200 ul. Take out only what you will use.
  • Pipet 1uL of the plasmid (or 5 ul of ligation reaction) you want to transform into an Eppendorf tube. Add MilliQ water to 10 ul.
  • When XL10 cells are thawed, pipet 100 uL into the tube with the plasmid. Pipet up and down to mix gently. Place tube on ice 30 minutes.
  • After incubating on ice for 30 minutes, place cells in incubator set to 42 C for 90s. (Use the water bath near the front sink in G308 – its temperature will be most accurate. This step must be done for EXACTLY 90 s).
  • Return the tube to ice for 2 min.
  • Add 1mL (1000uL) of LB to the tube.
  • Incubate at 37 C for 20-30 min.
  • Spread cells on plate with appropriate antibiotic: plate 200ul, 20ul in 80ul of LB broth, and 2ul in 98ul of LB broth. Let dry.
  • Place plates inverted in incubator at 37C overnight.

Notes

  • The competent cells we have made up are XL10-Gold – if we need to transfer them to DH5alpha at a later date we can retransform the final BioBricks
  • Can try 200 ul of cells instead of 100 ul to attempt to increase efficiency of transformation.