IGEM:MIT/2006/Introduction: Difference between revisions

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This page contains links to introductory information for the MIT iGEM team.
This page contains links to introductory information for the MIT iGEM team.


==Lab safety==
==Design==
'''All people working in a biological research lab must undergo safety training.'''
===System Design considerations===
*Feasible system scale (numbers of parts, plasmids, chassis types)
*Design tools - models, network diagrams
*Moving from system->devices->parts->DNA specification
*Likelihood of success - protein engineering, cloning, new biological techniques and new science etc.


To complete your online safety training, visit the [[Endy:Safety_Training | '''Endy lab safety training guide''']].  (Even if you have worked in a lab before, you should visit this page and verify that your training is up to date.)
===Abstraction hierarchy & standardization===
This should be done before your first day in lab.
*Parts - zinc fingers?
 
*Devices - receiver?, inverter?
Heather will be giving the lab-specific training <font color=red>- Day 1, Week 1</font>
*Systems - bacterial photography?
 
==Wiki==
'''How-to on wiki's'''
 
*[[OpenWetWare:Getting started | Getting started with wiki editing]] <font color=red>- Day 1, Week 1</font>
*Populate the official iGEM wiki
 
==Abstraction hierarchy==
*PoPS and composability
*PoPS and composability


==Registry==
==Build==
*Obtain accounts <font color=red>- Day 1, Week 1</font>
===Construction methods===
*Making a part (both basic and subpart) <font color=red>- Day 1, Week 1</font>
*BLAST
*Sequence alignments
 
==BioBricks assembly==
*[[BioBricks]] <font color=red>- Day 1, Week 1</font>
*[[BioBricks]] <font color=red>- Day 1, Week 1</font>
*Standard assembly <font color=blue>- Day 2, Week 1</font>
*Standard assembly <font color=blue>- Day 2, Week 1</font>
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*Direct synthesis
*Direct synthesis


==Part and device characterization==
===Construction tools===
*Registry
*#Obtain accounts <font color=red>- Day 1, Week 1</font>
*#Making a part (both basic and composite) <font color=red>- Day 1, Week 1</font>
*#BLAST
*#Sequence alignments
*NCBI Entrez  <font color=red>- Day 1, Week 1</font>
*VectorNTI
*Others?
 
==Test==
*Plate reader characterization (i.e. Receiver)
*Plate reader characterization (i.e. Receiver)
*Flow cytometry (i.e. Screening plasmid)
*Flow cytometry (i.e. Screening plasmid)
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*RT-PCR and Westerns
*RT-PCR and Westerns


==Searching and reading the literature==
==Necessary skills==
*[[Searching the literature]]
===Lab notebooks & documentation===
*[[OpenWetWare:Getting started | Getting started with wiki editing]] <font color=red>- Day 1, Week 1</font>
*Populate the [http://parts.mit.edu/wiki/index.php/MIT_2006 official MIT iGEM 2006 wiki page]
*The online lab notebook framework


==Lab techniques==
===Searching and reading the literature===
*[[Searching the literature]] <font color=green>- Day 3, Week 1</font>
 
===Lab safety===
*Complete the [[Endy:Safety_Training | '''Endy lab safety training''']].  (Even if you have worked in a lab before, you should visit this page and verify that your training is up to date.)  This should be done before your first day in lab.
*Heather will be giving the lab-specific training <font color=red>- Day 1, Week 1</font>


==Links==
==Links==
'''General introduction to ideas in Synthetic Biology'''
'''General introduction to ideas in Synthetic Biology'''
#[[Adventures | Adventures in synthetic biology comic]] --> Learn about PoPS
#[[Adventures | Adventures in synthetic biology comic]] --> Learn about PoPS
#[http://openwetware.org/images/0/0d/Nature04342.pdf Foundations for engineering biology] --> rant by Drew Endy
#[http://openwetware.org/images/0/0d/Nature04342.pdf Foundations for engineering biology] --> rant by Drew Endy
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#Find descriptions of [http://parts2.mit.edu/wiki/index.php/Igem_2005 2005 projects]
#Find descriptions of [http://parts2.mit.edu/wiki/index.php/Igem_2005 2005 projects]


==Week 1==
Goals -
*Do one assembly stage
*Make a biobrick
*Necessary software - VectorNTI, Registry, Wiki
*Literature searching


===Day 1===
==Schedules==
====Dry Lab====
*[[IGEM:MIT/2006/Introduction/Week 1]]
*Safety training
*Lab tour
*Registry accounts
====Wet Lab====
*Pick a gene and design primers
**Introduces parts
*Start overnights
**Introduces sterile technique, culturing,
===Day 2===
====Dry Lab====
*BioBricks Construction
====Wet Lab====
*Prep & Digest

Latest revision as of 12:14, 2 June 2006

This page contains links to introductory information for the MIT iGEM team.

Design

System Design considerations

  • Feasible system scale (numbers of parts, plasmids, chassis types)
  • Design tools - models, network diagrams
  • Moving from system->devices->parts->DNA specification
  • Likelihood of success - protein engineering, cloning, new biological techniques and new science etc.

Abstraction hierarchy & standardization

  • Parts - zinc fingers?
  • Devices - receiver?, inverter?
  • Systems - bacterial photography?
  • PoPS and composability

Build

Construction methods

  • BioBricks - Day 1, Week 1
  • Standard assembly - Day 2, Week 1
  • 3A assembly
  • In frame assembly
  • Direct synthesis

Construction tools

  • Registry
    1. Obtain accounts - Day 1, Week 1
    2. Making a part (both basic and composite) - Day 1, Week 1
    3. BLAST
    4. Sequence alignments
  • NCBI Entrez - Day 1, Week 1
  • VectorNTI
  • Others?

Test

  • Plate reader characterization (i.e. Receiver)
  • Flow cytometry (i.e. Screening plasmid)
  • Microscopy
  • RT-PCR and Westerns

Necessary skills

Lab notebooks & documentation

Searching and reading the literature

Lab safety

  • Complete the Endy lab safety training. (Even if you have worked in a lab before, you should visit this page and verify that your training is up to date.) This should be done before your first day in lab.
  • Heather will be giving the lab-specific training - Day 1, Week 1

Links

General introduction to ideas in Synthetic Biology

  1. Adventures in synthetic biology comic --> Learn about PoPS
  2. Foundations for engineering biology --> rant by Drew Endy
  3. MIT iGEM 2004 presentation (.ppt,pdf)
  4. UT Austin and UCSF 2004 project (coliroids)
  5. Find descriptions of 2005 projects


Schedules