Team:British Columbia/Notebook/Protocols
From 2013.igem.org
(Difference between revisions)
AnnaMüller (Talk | contribs) |
AnnaMüller (Talk | contribs) (→Gel Verification) |
||
Line 5: | Line 5: | ||
===[[Team:British_Columbia/Notebook/Protocols/gelverification|Gel Verification]]=== | ===[[Team:British_Columbia/Notebook/Protocols/gelverification|Gel Verification]]=== | ||
- | Make a gel and conduct gel elecrophoresis | + | Make a gel and conduct gel elecrophoresis |
===[[Team:British_Columbia/Notebook/Protocols/RepeatSpacerAssembly |CRISPR Repeat-Spacer Array Assembly]]=== | ===[[Team:British_Columbia/Notebook/Protocols/RepeatSpacerAssembly |CRISPR Repeat-Spacer Array Assembly]]=== |
Revision as of 00:18, 28 September 2013
iGEM Home
Protocols
PCR
Instruction for colony PCR and regular PCR
Gel Verification
Make a gel and conduct gel elecrophoresis
CRISPR Repeat-Spacer Array Assembly
Assemble combinatorial libraries of repeat-spacer-repeat arrays using oligonucleotides
Assembling Parts from Oligonucleotides
Assemble short parts from annealed oligonucleotides
(Multi) Site Directed Mutagenesis
Site directed mutagenesis. Protocol is directly amenable simultaneously making distant mutations.
Oligonucleotide Phosphorylation
Phosphorylate oligonucleotides prior to ligation
Electrocompetent Cell Production
Gas chromatography-mass spectrometry for biosynthetic product detection
GC-MS Protocol for assaying biosynthetic product production.
Make Combinatorial Part Libraries
Make combinatorial part libraries from compatible parts