Team:SDU-Denmark/Protocols

From 2009.igem.org

(Difference between revisions)
Line 1: Line 1:
{{:Team:SDU-Denmark/css}}
{{:Team:SDU-Denmark/css}}
 +
 +
<div id="container">
 +
{{:Team:SDU-Denmark/menu}}
{{:Team:SDU-Denmark/menu}}
 +
 +
<!-- LEFT CONTAINER -->
 +
<div id="leftcontent">
-
__NOTOC__
 
=Lé Protocols=
=Lé Protocols=
Line 25: Line 30:
[[Team:SDU-Denmark/Protocols/Ligations|Ligations]] - We used it for: Pasting our biobricks into backbones.
[[Team:SDU-Denmark/Protocols/Ligations|Ligations]] - We used it for: Pasting our biobricks into backbones.
 +
 +
 +
<!-- END LEFT CONTAINER -->
 +
</div>
 +
 +
<!-- RIGHT CONTAINER -->
 +
<div id="rightcontent">
 +
 +
__TOC__
 +
 +
<!-- END RIGHT CONTAINER -->
 +
</div>
 +
 +
 +
<!-- END MAIN CONTAINER -->
 +
</div>

Revision as of 18:45, 4 October 2009





Lé Protocols

Primer PCR protocol - We used it for: Making a full RIP molecule from our oligos.

Purification protocol from gel - We used it for: Gel purification, over and over and over.

Purification protocol from solution - We used it for: PCR product purification.

Making cells competent - We used it for: Making competent cells for both transformation and electroporation.

Transformation - We used it for: Transforming plasmids (containing biobricks) into competent cells.

Electroporation - We used it for: Transforming plasmids (containing biobricks) into competent cells. Electroporation is our preferred technique, since it requires less plasmid volume and uses electricity!

Miniprep - We used it for: Purifying plasmids from inoculations of transformed bacteria.

How to make an agarose gel - We used it for: Making Agarose gels, for use in testing brick and plasmid sizes. Very central technique to controlling your lab work.

Restrictions - We used it for: Cutting out biobricks and preparing backbones for insertion of biobricks.

Ligations - We used it for: Pasting our biobricks into backbones.


Contents