HTGAA
HTGAA
From the official webpage: Bio Academy is a Synthetic Biology Program directed by George Church, professor of Genetics at Harvard medical school. The Bio Academy is a part of the growing Academy of (almost) Anything, or the Academany.
It's a 15 week experimental course covering the major Synthetic Biology applications today.
HTGAA course 2017
2017 is the first year that the course is being taken by students at Hackuarium. The course is being followed by Daniel Hernandez and Thomas Jordan.
Important Links
Hackuarium Specific Links
Hackuarium Official Course Page: http://bio.fabcloud.io/hackuarium_2017/
Hackuarium Working Assignments Folder: https://drive.google.com/open?id=0B26FGn9YdUxQVmZuaTBNNWlGR0k
General Course Links
Course page: http://bio.fabcloud.io/2017/ This includes all the weekly lectures and homework discussions in the left-hand sidebar. At the bottom there are additional learning resources.
Students: https://docs.google.com/spreadsheets/d/1WRnoyLbWejQslRvaRNfQBxJkjgmKWHNfFT9BOZqdEGM/edit#gid=0
Curriculum: https://docs.google.com/spreadsheets/d/1Xg_GtrFb8wYJVUPlrbUb6pP0dWGmkoAKU4xP6qhBKVE/edit#gid=0
Recommended Hardware: https://docs.google.com/spreadsheets/d/1iu57Ct9NiPPVxzK_PBd_JlX4dlB68pQOxFCOnThnZPs/edit#gid=0
Weekly topics / Experiments
wk1: Principles and Practices
Link to weekly page: http://bio.fabcloud.io/2017/principles_practices_hardware.html
wk2: Bio Design / Plasmid digest
Theory class: George Church spoke about the capacity to modify biological material/organisms.
Lab Task: Design and verify restriction digest of a circular DNA plasmid by gel electrophoresis. Compare your experimental result with what you would predict from the plasmid map.
Link to weekly page: http://bio.fabcloud.io/2017/bio_design.html
The protocol designed for this experiment is:
https://docs.google.com/document/d/1Rs1ElrSjuLlmIEhpxZ6856ivZJBkXE4BnWnDYquZZ0w/edit?usp=sharing
The experiment was carried out on wednesday, 11th of of October 2017 with the help of Rachel.
The gel prepared was 20 mL of 1% agarose -1x TAE buffered gel. It was prepared by dissolving 0.2g of agarose inside 20 mL of a 1x TAE buffer solution. Upon boiling of the gel, SYBR safe dye was added and the liquid cast into the makeshift box. The Gel contained: