Team:British Columbia/Notebook/Protocol
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Revision as of 22:48, 17 October 2014
- <a href="https://2014.igem.org/Team:British_Columbia/Notebook/Protocols/PCR">PCR</a>
- <a href="Team:British_Columbia/Notebook/Protocols/gelverificaation">Gel Verification</a>
Instruction for colony PCR and regular PCR
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Make a gel and conduct gel elecrophoresis
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Restriction digest with BioBrick plasmid an inserts
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Ligate Biobrick insert to vector
</br>
Make LB plates with antibiotics
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Make liquid LB media
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Preparation of chemically competent cells
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Transformation of plasmi DNA into chemically competent cells
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Assemble combinatorial libraries of repeat-spacer-repeat arrays using oligonucleotides
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Assemble short parts from annealed oligonucleotides
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Site directed mutagenesis. Protocol is directly amenable simultaneously making distant mutations.
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Phosphorylate oligonucleotides prior to ligation
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Make electrocompetent cells
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Make combinatorial part libraries from compatible parts
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