IGEM:Harvard/2006/Cyanobacteria/Notebook/2006-8-25: Difference between revisions

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== E-gel image of \X and \X-P digests of Nick's KaiB + J04500 ligations ==
== E-gel image of \X and \X-P digests of Nick's KaiB + J04500 ligations ==
I forgot to run the undigested plasmid on this gel, but by comparing the \X and \X-P digests, it appears we still don't have insert.
[[Image:cyano 2006-8-25 KaiB J04500 X X-P.jpg|thumb|left|Click for legend]]

Revision as of 21:24, 25 August 2006

Miniprep of Nick's cultures #5 and #8

I miniprepped the 4 cultures Nick inoculated last night, and labeled them 5-1, 5-2, 8-1, and 8-2.

From Nick's email:

All three colonies are KaiB constructs. I have made 4 overnight cultures with the following labels:

"NES 5" is a putative KaiB insert in a J04500 from a 6:1 Insert:Backbone reaction using the NEB ligase. "NES 5" is a second culture started from the same colony. "NES 8" is a putative KaiB insert in a J04500 from a 3:1 Insert:Backbone reaction using the Roche ligase. "NES 8" is from a different (*not* clonal) colony from the same ligation reaction as the other NES 8.

Diagnostic digests of Nick's cultures #5 and #8

Digest # Plasmid Enzymes
1 5-1 X
2 5-1 X, P
3 8-1 X
4 8-1 X, P
5 8-2 X
6 8-2 X, P

\X digest reactions

  • 19.5 µL DNA
  • 2.25 µL H2O
  • 2.5 µL NEBuffer 2
  • 0.5 µL XbaI
  • 0.25 µL 100x BSA

\X digest master

  • 9 µL H2O
  • 10 µL NEBuffer 2
  • 2 µL XbaI
  • 1 µL 100x BSA

Pipette 5.5 µL into each reaction.

\X-P digest reactions

  • 19.5 µL DNA
  • 1.75 µL H2O
  • 2.5 µL NEBuffer 3
  • 0.5 µL XbaI
  • 0.5 µL PstI
  • 0.25 µL 100x BSA

\X-P digest master

  • 7 µL H2O
  • 10 µL NEBuffer 3
  • 2 µL XbaI
  • 2 µL PstI
  • 1 µL 100x BSA

Pipette 5.5 µL into each reaction.

Digested for 6 hours at 45C, set to finish around 2300 tonight.

Restreak and colony PCR

I restreaked, colony PCR'd, and inoculated 10 colonies from Nick's ligation #5 that he plated on 2006-8-24 (bottom of link). They are restreaked on two plates.

Ligation conditions:

KaiC Gel + Gel Backbone #5 II at 17C

Colony PCR reaction

  • 8 uL PCR supermix
  • 1 uL VF2 primer
  • 1 uL VR primer

Colony PCR master mix

  • 88 uL PCR supermix
  • 11 uL VF2 primer
  • 11 uL VR primer

Pipette 10 uL into each reaction.

Colony PCR schedule

  • 95C for 15'00
  • Do 30 times:
    • 95C for 0'30
    • 55C for 0'30
    • 72C for 2'00
  • 72C for 10'00
  • 4C forever

E-gel image of colony PCRs

It looks like the colonies don't contain our plasmid.

Click for legend


E-gel image of \X and \X-P digests of Nick's KaiB + J04500 ligations

I forgot to run the undigested plasmid on this gel, but by comparing the \X and \X-P digests, it appears we still don't have insert.

Click for legend