Team:Washington/Notebook
From 2009.igem.org
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{{Template:Team:Washington/Templates/Header}} | {{Template:Team:Washington/Templates/Header}} | ||
- | = | + | = '''Protocols''' = |
[[Team:Washington/Notebook/protein_gel|Protein Gel]] | [[Team:Washington/Notebook/protein_gel|Protein Gel]] | ||
- | [[Team:Washington/Notebook/Microscope| | + | [[Team:Washington/Notebook/Microscope|Microscopy]] |
[[Team:Washington/Notebook/Flow_Cytometry|Flow Cytometry]] | [[Team:Washington/Notebook/Flow_Cytometry|Flow Cytometry]] | ||
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[[Team:Washington/Notebook/colony_PCR|Colony PCR]] | [[Team:Washington/Notebook/colony_PCR|Colony PCR]] | ||
- | [[Team:Washington/Notebook/NheI_PstI| | + | [[Team:Washington/Notebook/NheI_PstI|BioBrick Assembly using the NheI and PstI sites]] |
- | [[Team:Washington/Notebook/NheI| | + | [[Team:Washington/Notebook/NheI|BioBrick Assembly using the NheI site]] |
+ | [[Team:Washington/Notebook/SOEingPCR|SOEing PCR]] | ||
- | + | [[Team:Washington/Notebook/IMAC_protocol|Traditional Protein Purification (IMAC)]] | |
- | + | ||
+ | [[Team:Washington/Notebook/Standard_curve|Generating a Standard curve for GFP concentration]] | ||
- | = | + | <br> |
+ | |||
+ | = '''Project Time Line''' = | ||
Latest revision as of 20:20, 20 October 2009
Protocols
Supernatant Protein Purification, 50mL
Supernatant Protein Purification, 2mL
BioBrick Assembly using the NheI and PstI sites
BioBrick Assembly using the NheI site
Traditional Protein Purification (IMAC)
Generating a Standard curve for GFP concentration
Project Time Line
- Winter Quarter
- Introduction to iGEM
- Synthetic Biology Seminar
- Plan for project ideas
- Spring Quarter
- Narrow down potential projects
- Choose Project
- Order oligos and start synthesizing genes
- Obtained Funding
- Stock Lab
- June
- Sequence genes
- Preliminary binding assays for biotinylated fluorophore
- Introduction to Fold-it as a tool for protein design
- Test target proteins for solubility and expression
- Start assembly of secretion genes
- July
- Develop and perform assays for testing legacy surface display bio-bricks
- Transfer prtDEF contig from secretion system into low copy plasmid
- Test target proteins for functionality
- August
- Finish assembly of secretion system
- Start cell lines containing various forms of secretion system, make competent
- Transform competent cells containing secretion system with target vector
- Test for secretion of target protein
- Start design of new display construct
- September
- Switch secretion system into new cell line, make cells competent
- Transform with target vector
- Test for secretion
- Start Presentation
- Start t-shirt design
- Insert streptavidin into new display vector
- October
- Fine tune secretion assay, adjust controls
- Finalize characterization of legacy parts
- Practice presentation
- Characterize target bio-bricks
- Prepare for Jamboree