Illinois/17 July 2008
From 2008.igem.org
(Difference between revisions)
(New page: '''Antibody/GPCR Fusion''' *Consulting meeting with Huimin Zhao (Associate Professor, Chemical and Biomolecular Engineering)) |
|||
Line 1: | Line 1: | ||
'''Antibody/GPCR Fusion''' | '''Antibody/GPCR Fusion''' | ||
*Consulting meeting with Huimin Zhao (Associate Professor, Chemical and Biomolecular Engineering) | *Consulting meeting with Huimin Zhao (Associate Professor, Chemical and Biomolecular Engineering) | ||
+ | |||
+ | '''LAB WORK''' | ||
+ | |||
+ | '''Receptor Tyrosine Kinase method''' | ||
+ | |||
+ | E.Coli Media | ||
+ | |||
+ | LB medium, per liter | ||
+ | |||
+ | 10g tryptone | ||
+ | |||
+ | 5g yeast extract | ||
+ | |||
+ | 5g NaCl | ||
+ | |||
+ | 1 mL 1N NaOH | ||
+ | |||
+ | 15g (agar for plates) | ||
+ | |||
+ | 1. antibody DNA resuspended in TE buffer, 0.1 μg/μL | ||
+ | |||
+ | 2. 5mL LB inoculated with single colony DH5a pro | ||
+ | |||
+ | 3. Incubated at 37 degrees overnight |
Latest revision as of 15:49, 30 July 2008
Antibody/GPCR Fusion
- Consulting meeting with Huimin Zhao (Associate Professor, Chemical and Biomolecular Engineering)
LAB WORK
Receptor Tyrosine Kinase method
E.Coli Media
LB medium, per liter
10g tryptone
5g yeast extract
5g NaCl
1 mL 1N NaOH
15g (agar for plates)
1. antibody DNA resuspended in TE buffer, 0.1 μg/μL
2. 5mL LB inoculated with single colony DH5a pro
3. Incubated at 37 degrees overnight