"
Team:Tsinghua/Experiment1
From 2009.igem.org
(Difference between revisions)
(→Bottom-Up Approach) |
|||
| Line 5: | Line 5: | ||
Specifically, we choose two molecular cloning vectors to encode two sections of the gene therapy vector genome, pET28a and pACYCDuet1. | Specifically, we choose two molecular cloning vectors to encode two sections of the gene therapy vector genome, pET28a and pACYCDuet1. | ||
| - | [[Image:pET28a.jpg| | + | [[Image:pET28a.jpg|450px|pET28a]] |
| - | [[Image:pACYCDuet1.jpg| | + | [[Image:pACYCDuet1.jpg|450px|pACYCDuet1]] |
==Top-Down Approach== | ==Top-Down Approach== | ||
=GenSniper Production Evaluation= | =GenSniper Production Evaluation= | ||
Revision as of 05:50, 3 October 2009
Contents |
Synthesis of the Gene Therapy Production System
Bottom-Up Approach
In the bottom-up approach, we amplify the biobricks from both the bacteriophage lambda and the adenovirus genome and incorporate them with a given order into molecular cloning vector(s).
Specifically, we choose two molecular cloning vectors to encode two sections of the gene therapy vector genome, pET28a and pACYCDuet1.
