Team:Washington/Notebook

From 2009.igem.org

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A ROUGH TIMELINE OF THE PROJECT!
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==== Time Line of Project ====
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*Winter Quarter
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{{Template:Team:Washington/Templates/Footer}}
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**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
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*July
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**Develop and perform assays for testing legacy surface display bio-bricks
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**Transfer prtDEF contig from secretion system into low copy plasmid
 +
**Test target proteins for functionality
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*August
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**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 construt

Revision as of 04:52, 15 October 2009

Uw title logo.png

Protocols

Protein Gel

Microscope

Flow Cytometry

Supernatant Protein Purification, 50mL

Ni-column Set up

Supernatant Protein Purification, 2mL

Gene Synthesis

Colony PCR

Gene Assembly using the NheI and PstI sites

Gene Assembly using the NheI site


Time Line of Project

  • 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 construt