Team:Nevada/Week 17
From 2012.igem.org
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Contents |
September 10
- Michelle:
- Single colony isolation of M2-BL21 from LB AMP-CM stock plate, which was followed by culturing it in 10ml LB :::AMP-CM broth and then large scale culturing with 50ml of LB AMP-CM broth.
- Justin and Dafne:
- Proteins were separated from cells (as done before)
- Suspended in Amylose column buffer
- proteins were purified using Amylose Resin High Flow (NEB)
- eluted using 1M glycine: pH 10 buffer
September 11
- Joe:
- harvest protein from RFP-SBP
- Justin and Dafne
- Concentrate protein using Desalting column
- Jeremiah & Chris:
- Express BL21 cells by use of a L. Arabanose gradient
- Took and 8 hour and overnight time sample
September 12
· Run samples on a polyacrylamide gel · Western blot protocol
September 13
Joe: Add rice to purified protein, incubate for 5 hours
Not enough protein - did not work
Michelle:
Glycerol stocked M2-BL21 before large scale culturing M2-BL21 with 50ml LB AMP-CM broth.
September 14
Joe: make 10, 10 ml cultures of RFP-SBP in Top10 cells
Michelle:
Transformed M2 (SBP-LRP) into BL21 cells and plated on LB AMP-CM plates.
Jeremiah & Chris: · Develop western o No band appeared because the BL21 cells needed to be grown in Ampicillin (Amp) and Chloramphenicol (Cm) antibiotics · Minipre fresh expression plasmid with TBP+ from BL21 culture o Ran on a gel (gel #193) · Transform plasmid into new BL21 cells o Use Amp and Cm antibiotics when plating · Prepare submission plasmid (pBP31C) o Miniprep and digest in large quantities as to have enough for the other groups
Chris and Jeremiah:
· Colony PCR check 5 samples
o Ran on a gel (gel #195)