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Team:Brasil-SP/Notebook/Protocols
From 2014.igem.org
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<li><a href="https://static.igem.org/mediawiki/2014/7/74/PCR.pdf">PCR</a></li> | <li><a href="https://static.igem.org/mediawiki/2014/7/74/PCR.pdf">PCR</a></li> | ||
<li><a href="https://static.igem.org/mediawiki/2014/a/af/Agarose_Gel_Electrophoresis_and_DNA_Gel_Purification.pdf">Agarose Gel Electrophoresis and DNA Gel Purification</a></li> | <li><a href="https://static.igem.org/mediawiki/2014/a/af/Agarose_Gel_Electrophoresis_and_DNA_Gel_Purification.pdf">Agarose Gel Electrophoresis and DNA Gel Purification</a></li> | ||
| - | <li><a href="https://static.igem.org/mediawiki/2014/0/03/ | + | <li><a href="https://static.igem.org/mediawiki/2014/0/03/PCR_Product_Cloning.pdf">PCR Product cloning</a></li> |
| - | <li><a href="https://static.igem.org/mediawiki/2014/9/96/Competent_Cells_using_Calcium_Chloride.pdf">Competent Cells using Calcium Chloride</a></li> | + | <li><a href="https://static.igem.org/mediawiki/2014/9/96/Competent_Cells_using_Calcium_Chloride.pdf">Competent <i>E. coli</i> Cells using Calcium Chloride</a></li> |
<li><a href="https://static.igem.org/mediawiki/2014/a/a5/Transformation_in_Escherichia_coli_DH5.pdf">Transformation in <i>E. coli</i> DH5-alpha</a></li> | <li><a href="https://static.igem.org/mediawiki/2014/a/a5/Transformation_in_Escherichia_coli_DH5.pdf">Transformation in <i>E. coli</i> DH5-alpha</a></li> | ||
<li><a href="https://static.igem.org/mediawiki/2014/a/ac/Plasmid_preparation_by_alkaline_lysis_and_SDS.pdf">Plasmid preparation by alkaline lysis and SDS</a></li> | <li><a href="https://static.igem.org/mediawiki/2014/a/ac/Plasmid_preparation_by_alkaline_lysis_and_SDS.pdf">Plasmid preparation by alkaline lysis and SDS</a></li> | ||
<li><a href="https://static.igem.org/mediawiki/2014/7/7a/Cohesive-end_assembly_cloning.pdf">Cohesive-end assembly cloning</a></li> | <li><a href="https://static.igem.org/mediawiki/2014/7/7a/Cohesive-end_assembly_cloning.pdf">Cohesive-end assembly cloning</a></li> | ||
<li><a href="https://static.igem.org/mediawiki/2014/4/42/Restriction_Anaysis_and_Digestion_in_large_scale.pdf">Restriction Analysis and Digestion in large scale</a></li> | <li><a href="https://static.igem.org/mediawiki/2014/4/42/Restriction_Anaysis_and_Digestion_in_large_scale.pdf">Restriction Analysis and Digestion in large scale</a></li> | ||
| + | <li><a href="https://static.igem.org/mediawiki/2014/8/8e/Bacillus_competent_cells.pdf">Competent <i>Bacillus subtilis</i> cells</a></li> | ||
</ul> | </ul> | ||
Revision as of 18:27, 11 October 2014
The content of this page is merely provisional!
Well... the page title describe the page by itself!
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Lab Protocols
| Characterization ProtocolsMeasurement Interlab StudyAs part of the first international interlab measurement study in synthetic biology, all Measurement Track teams were required to obtain fluorescence data for three specific genetic devices. They are
| Biobrick device 1: BBa_I20260, an existing device Assembly Protocol Biobrick Device 1
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| Biobrick device 2: BBa_J23101 + BBa_E0240, a new device built by each team Assembly Protocol Biobrick Device 2 and 3
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| Biobrick device 3: BBa_J23115 + BBa_E0240, a new device built by each team. Assembly Protocol Biobrick Device 2 and 3
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