Team:University College London/LabBook/Week4
From 2012.igem.org
(Difference between revisions)
(Created page with "{{:Team:University_College_London/templates/headimg|coverpicture=images/a/a1/Ucl2012-labbook-title.png}}<html><script type="text/javascript" src="https://2012.igem.org/wiki/index....") |
Rwilkinson (Talk | contribs) (→4.1) |
||
Line 4: | Line 4: | ||
<img src="https://static.igem.org/mediawiki/2012/b/b0/Ucl2012-labbook-graph4-1.png" /> | <img src="https://static.igem.org/mediawiki/2012/b/b0/Ucl2012-labbook-graph4-1.png" /> | ||
<div class="experimentContent"></html> | <div class="experimentContent"></html> | ||
- | == 4.1 == | + | == Wednesday (4.7.12)== |
+ | |||
+ | '''Aim - Transformation of Key Aggregation Module BioBricks:''' Expt 4.1 will be transforming the Curli Cluster, Green Fluorescence Protein and Ribosome Binding Site BioBricks into our W3100 competent cell line. Transformed cells will be cultured under the selective pressure of antibiotic, after which the plasmids are purified and the presence of the correct BioBricks will be diagnosed with an Analytical Restriction Enzyme Digest and Gel Electrophoresis. | ||
+ | |||
+ | '''Method''' | ||
+ | (LOGO) Transformation Protocol 1 | ||
+ | |||
+ | {| class="wikitable" | ||
+ | |- | ||
+ | ! colspan="2" | !! Function !! Module | ||
+ | |- | ||
+ | | rowspan="3" |BioBrick|| BBa_I13522 || Green Fluorescence Protein(GFP) || Aggregation | ||
+ | |- | ||
+ | | BBa_B0034 || Ribosome Binding Site (RBS)|| All | ||
+ | |- | ||
+ | | BBa_K540000 || (rcn-csg BAEFG curli cluster) || Aggregation | ||
+ | |- | ||
+ | | Control || No BioBrick|| || | ||
+ | |} | ||
+ | |||
+ | Step 1 – Thawing Cells: Use W3100 cell line created in Week 2 (Expt 2.1) | ||
+ | Step 3 – Addition of BioBrick: To each 2ml eppendorf, add 1ul of the following BioBricks. Include an extra tube as a control, with no BioBrick added. | ||
+ | |||
<html></div> | <html></div> | ||
<div class="experiment"></div></html> | <div class="experiment"></div></html> | ||
{{:Team:University_College_London/templates/foot}} | {{:Team:University_College_London/templates/foot}} |
Revision as of 15:51, 1 August 2012
Wednesday (4.7.12)
Aim - Transformation of Key Aggregation Module BioBricks: Expt 4.1 will be transforming the Curli Cluster, Green Fluorescence Protein and Ribosome Binding Site BioBricks into our W3100 competent cell line. Transformed cells will be cultured under the selective pressure of antibiotic, after which the plasmids are purified and the presence of the correct BioBricks will be diagnosed with an Analytical Restriction Enzyme Digest and Gel Electrophoresis.
Method (LOGO) Transformation Protocol 1
Function | Module | ||
---|---|---|---|
BioBrick | BBa_I13522 | Green Fluorescence Protein(GFP) | Aggregation |
BBa_B0034 | Ribosome Binding Site (RBS) | All | |
BBa_K540000 | (rcn-csg BAEFG curli cluster) | Aggregation | |
Control | No BioBrick |
Step 1 – Thawing Cells: Use W3100 cell line created in Week 2 (Expt 2.1) Step 3 – Addition of BioBrick: To each 2ml eppendorf, add 1ul of the following BioBricks. Include an extra tube as a control, with no BioBrick added.