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From 2012.igem.org

week 2: 7 may - 11 may

office work

This is our first full week to work on this amazing project. There are four of us who can work whole days (Robert, Jeroen, Kees and Mark) and two of us who can work in the afternoon (Thijs and Wouter), the others will start when the sixth period end of our academic year.

[meeting]

This week we searched for programs which can predict the tertary structure of the monomers of the VLPs, we found several of them, but phyre2 really stand out with the simple fill in sheat and the possibility to download the PDB files of your predicted protein. Besides searching for programs, we also worked on the protocols we are going to use and check if we've got the required equipment and materials. Thijs and Mark worked also on the logo for the team and the backbone for the wiki.

lab work

7 may

E. coli in liquid LB

3 plates per strain were picked and grown in 25 ml LB. all plates grown well accept for amp plates, due to drying effects.

8 may

10:00 Continue growth. All 3 strains in shaker, 180 RPM, 30 degree celcius.

4 x 1 L SOB is made

16:55 culture mach1 and DH5X are plated 10x and 1000x diluted on LB plates. Dilutions are done with demi water.

Plates were placed in 37 degree Celcius stove

9 may

9:15 10x dilution was to low, overgrown 1000x was nearly overrown, but still acceptable.

picked 1 MACH1 and 1 DH5X colony and grown in 10 ml SOB medium, 37 degree Celcius, 180 RPM

10 may

MACH1 competent cells followin pinky's protocol. with the following diviations

• 4x 500 ml SOB
• SLA 3000 rotor

OD harvest at: 0.5 -0.45

11 may

CCMV protocol inoculated at 8:45 IPTG at 11:45

centrifugation in greiner tubes

pellet stored at -20 degree Celcius, 50 ml greiner tubes

Miniprep following the Gene Jet Fermentas protocol

• pet28
• standard 10 stock 1
• standard 10 stock 7