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<li> Region: Europe </li> | <li> Region: Europe </li> | ||
<li> Application Date: 2015-02-21 </li> | <li> Application Date: 2015-02-21 </li> | ||
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Latest revision as of 22:19, 17 November 2015
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Synthetic Biology
based on standard parts
based on standard parts
X
Team Information - Columbia NYC
▼ General
Schools
?
- Stanford University Online High School, CA, USA ohs.stanford.edu
- Hankuk Academy of Foreign Studies Kyunggi, Korea www.hafs.hs.kr
- Cheongshim International Academy, Kyunggi, Korea http://www.csia.hs.kr/
Team Status
?
- ✔ Your registration fee has been received
- ✔ Shipping information has been entered
- ✔ Resource description has been submitted
Location
- Section: ? Undergraduate
- Region: Europe
- Application Date: 2015-02-21
- Acceptance Date: 2015-04-13 14:21:14
▼Contact
▼ Deadlines
Primary Instructor (PI)
?
☺
Jiandong Jiang ✆
+3472349823749 ✉
@njau.edu.cn
Secondary Instructor
?
☺
Jiandong Jiang ✆
+3472349823749 ✉
@njau.edu.cn
Student Leader
?
☺
Jiandong Jiang ✆
+3472349823749 ✉
@njau.edu.cn
May
- ✔ 10 Check In Form
June
- ! 10 Visa Application Day
- ! 19 InterLab Measurement study sign up
- ✔ 22 About our Lab form
- ✔ 25 About our Project form
July
- ✘ 15 About our Project form
- ✘ 15 Project descriptiondue
August
- ✘ 07 Track selection due
- ✘ 07 Title and abstractdue
- ✔ 28 Final Safety form
September
- ! 10 Team banners due
- ✔ 11 Team rostersdue
- ✘ 18 Part submission send by date
- ✘ 18 Judging form due
- ! 18 Wiki freeze
- ✔ 11 Keywordsdue
October
- ! 31 Wiki freeze archive
Assigned Track
New Application
Track Preferences
?
- New Application
- Manufacturing
- Measurement
Part Numbers
BBa_K1606000
to
BBa_K1606999
Keywords
?
- Insects
- toolkit
- Spodoptera frugiperda
Title and Abstract
?
The purpose of this project is to introduce the Sf9 cell line (Fall armyworm ovary, Spodoptera frugiperda cells) to synthetic biology and the iGEM Competition, by developing a tool kit of several biobricks for their use in this new chassis. We will use the Sf9 cells as an alternative for the production of proteins with high complexity and post-traductional modifications, because of their flexibility, cultivation time and minor cost compared with other expression systems. We will characterize functional parts for two main areas: Transfection and Genome Editing. For the first part we will characterize baculovirus mediated transfection and, direct plasmid transfection for the generation of stable cell lines; for the second part we will use the CRISPR/Cas9 system to assay highly specific genome modifications in an effort to improve production and ease of use of this technology.
Instructors
?
Students
?
Medals
Gold
Awards
Best Manufacturing Project, Overgrad
Nominations
Best Manufacturing Project, Overgrad
Best Software Tool, Overgrad
Best Part Collection, Overgrad