BE.109:DNA engineering

From OpenWetWare

(Difference between revisions)
Jump to: navigation, search
(DNA engineering web links)
(DNA engineering web links)
Line 46: Line 46:
pCX-EGFP plasmid map: [[Image:Macintosh_HD-Users-nkuldell-Desktop-pCX-EGFP.doc|pCX-EGFP.doc]]
pCX-EGFP plasmid map: [[Image:Macintosh_HD-Users-nkuldell-Desktop-pCX-EGFP.doc|pCX-EGFP.doc]]
[[Image:Experimental Overview.jpg|thumb|left|500px|]]
<br style="clear:both" />
<br style="clear:both" />

Revision as of 00:59, 9 February 2006

BE.109 Laboratory Fundamentals of Biological Engineering

Image:BE LongImage-1.jpg

Home        Getting started        Lab        Presenting your work        People        Schedule       

DNA engineering        Protein engineering        Systems engineering        Bio-material engineering       


Module 1

Instructors: Bevin Engelward and Natalie Kuldell

TA: Yoon Sung Nam

In this experimental module you will modify the gene for EGFP (Enhanced Green Fluorescent Protein) to truncate the protein it encodes. Cells expressing the full-length protein glow green when exposed to light of the appropriate wavelength. You will be designing and then creating an expression vector to delete the first 32 amino acids of EGFP. Cells transfected with your expression vector should not glow green, a prediction you will test. You will also test whether this N-terminally truncated EGFP can recombine with a C-terminally truncated version to regenerate full length EGFP in vivo. Finally, you will have the opportunity to suggest changes to the experimental protocol that will increase the frequency of green cells in which there has been an inter-plasmid recombination event. We will then choose a few variables to test on the final day of the experiment.

Recombocell Image from Dominika Wiktor of the Engelward Lab
Recombocell Image from Dominika Wiktor of the Engelward Lab

A schematic overview of this module is below.

Lab handouts

Day 1: DNA engineering using PCR (you will also need weblinks, below)

Day 2: Clean and cut DNA

Day 3: Agarose gel electrophoresis

Day 4: DNA ligation and bacterial transformation

Day 5: Examine candidate clones

Day 6: Restriction map and tissue culture

Day 7: Lipofection

Day 8: FACS analysis

Module 1 lab report schedule

DNA engineering web links

Engelward lab resources:

pCX-EGFP plasmid map: Image:Macintosh HD-Users-nkuldell-Desktop-pCX-EGFP.doc

Image:Macintosh HD-Users-nkuldell-Desktop-pCX-EGFP.doc

ORF finder:



New England Biolabs:


Note: PDF reprints are provided below within the context of fair use. Please obtain copies from the publisher if appropriate.

  1. Pathways for mitotic homologous recombination in mammalian cells
    Mutation Research 27 November 2003 DOI:10.1016/j.mrfmmm.2003.08.013
    Thomas Helleday
    PDF reprint
Personal tools