Montreal/Notebook/June

From 2008.igem.org

Revision as of 19:34, 17 June 2008 by Sayehd (Talk | contribs)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Home The Team The Project Parts Submitted to the Registry Modeling Notebook

June 2008
Su M T W Th F Sa
1 2 3 4 5 6 7
8 9 10 11 12 13 14
15 16 17 18 19 20 21
22 23 24 25 26 27 29
29 30


Contents

June 2008

June 2

  • Growth of I-brick on culture
  • Midi-prep of both I and J brick followed by gel
  • Gel indicates no presence of DNA, will be confirmed by spectrophotometric assay

June 3

  • Seeding of 5mL cultures of both I and J brick
  • Identity of colonies on I brick plates is suspect, must ensure that eventual DNA gel confirms exact restriction digest

June 4

Midiprep was done on the I and the J-brick. Once the isopropanol was added, the J-brick midiprep looked clear (no DNA was eluted). DNA gel needs to be done to confirm presence of DNA in both cases.

June 9

  • Seeded J and I-brick re-seeded for Maxi-Prep
  • Gel failed to confirm presence of previously collected DNA samples of J and I-brick, will be repeated following Maxi-Prep.

June 10

Since no growth was observed in the I-brick culture, the I brick was re-seeded. The J-brick was diluted in 500-ml of LB broth(for a Maxiprep to be done the next day).

June 11

  • Maxiprep of the J-brick.
  • Restriction digest of J-brick.
  • Dilution of I-brick in 500-ml of LB broth.

June 12

  • Maxiprep of the I-brick.
  • Restriction digest and gel of June 11th and June 12th I-brick and J-brick DNA using EcoR1. Bands revealed at roughly 4000bp and 2500bp for I-brick (expected 2652bp and 3939bp). J brick single band that was not informative, new digestion to be completed tomorrow.

June 16

  • I-brick was seeded and diluted over last two days, but there was insufficient growth so it will be left to grow one more day before performing another midi-prep. This is to compliment the already successful Maxi-Prep that gave low concentrations of DNA.
  • Another gel was performed of previous J-brick preps that confirmed the absence of the desired plasmid, no DNA was detected when digested with EcoR1.
  • J-brick was re-transformed into TOP10 chemically competent cells and then plated on Amp+ plates.

June 17

  • The J-Brick was re-seeded since when a gel was ran on the J-Brick, no DNA was observed.
  • J-Brick plate was left out to maximize its growth overnight.
  • More antibiotic was added to the I-Brick culture (since it did not grow in LB broth for the past two days) and it was transferred from a Falcon tube to an Erlenmeyer Flask to maximize its growth.