Team:Stanford/Notebook/Lab Work/Week 5

From 2010.igem.org

(Difference between revisions)
(Laura's Notebook)
(7/30 Friday)
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==7/30 Friday==
==7/30 Friday==
 +
 +
=== Laura's Notebook ===
 +
'''9am iGEM meeting'''
 +
in attendance: team (Chris, Karina, Alex, Greg, Francisco, Laura), Christina, Ryan, Rayka, Anusuya, Graham
 +
Things to accomplish/address by next week:
 +
*potential names of circuits (Laura, Rayka)
 +
*flow cytometry: Does Scanford work for E. Coli? (Chris, Graham)
 +
*get ligations to work! (everyone)
 +
**make sure DNA concentration is high enough
 +
**when looking at gel to estimate concentration, look directly at gel (not at image on computer screen)
 +
**use fresh ligase buffer (or add ATP)
 +
**get successful ligation to use as positive control (from Ryan?)
 +
*get RSID1C PCR working
 +
**check concentration of primers: mix well, make new working stock
 +
**double check annealing temperatures, correct sequences
 +
*4 piece PCR (Alex)- order as 2 pieces?
 +
*circuit diagrams, including levels of abstraction, consistent formats
 +
*Twitter:
 +
**list/group
 +
**record audio (in as many languages as possible)
 +
</div>
</div>

Revision as of 20:55, 4 August 2010

Contents

7/26 Monday

Laura's Notebook

helped Francisco aliquot competent cells (thaw main tube- 1 mL- on ice, transfer 50 uL to each of 20 pre-chilled 0.5 mL microfuge tubes)


7/27 Tuesday

Laura's notebook

redo failed ligation: vary vector/insert ratios

prior recipe ligation 1 ligation 2 ligation 3
water none 11.0 7.0 none
vector 5.0 2.0 2.0 2.0
insert 12.0 4.0 8.0 15.0
10X buffer 2.0 2.0 2.0 2.0
ligase 1.0 1.0 1.0 1.0
  • vector=B1006 linearized (cut with EcoRI, XbaI; inserts=GFP or RFP cut with EcoRI, SpeI (6 ligations set up)
  • Francisco transformed these


7/28 Wednesday

Laura's Lab Notebook

miniprepped (ProMega kit): GFP and B1006 terminator (RFP didn't grow) NanoDrop data:

sample 260/280 260/230 ng/uL
B1006 1.61 0.95 49.4
GFP 1.83 1.22 96.4

ran 2% diagnostic gel, 75V, 1 hour

  • order: 100bp ladder, RSID1C PCR product, GFP digestion, RFP digestion, terminator digestion
  • all samples: 1 uL sample + 1 uL loading dye

ran 2% gel for gel extraction, 75V, 1 hour

  • order: 100bp ladder, GFP digestion, RFP digestion
  • 10 uL loading dye added to 50 uL digestions, 40 uL loaded on gel

gel extraction of GFP, RFP digestion products (Qiagen kit)

tube (g) tube + slice (g) gel slice (g) uL QG
GFP 1.01 1.03 0.02 60
RFP 1.01 1.03 0.02 60

ran 2% diagnostic gel of gel purified GFP and RFP digests

  • order: 100bp ladder, GFP, RFP
  • 1 uL sample + 1 uL dye + 4 uL H2O

B1006 terminator NanoDrop data (diluted 50:50 with H2O)

260/280 260/230 ng/uL
1.47 1.39 10.4
  • = 20.8 ng/uL in original sample

Digest concentrations still very low... set up larger overnight cultures- 9 mL cultures, 2 cultures each part:

  • B1006 (terminator)
  • GFP
  • RFP
  • pBAD (I0500)
  • pLUX (F2620)

7/29 Thursday

Laura's Notebook

Miniprepped (ProMega kit): RFP, GFP, B1006 terminator, F2620 (pBAD didn't grow)

  • all 18 mL (2- 9mL cultures) combined into one miniprep for each
  • Francisco did nanodrop: he has concentration data

set up digestions for both types of ligations (two-part and 3a protocol)

  1. RFP and GFP: cut with EcoRI, SpeI (2 digestions each)
  2. B1006 terminator: cut with EcoRI 2 hours, heat kill 80oC 20 minutes, then add XbaI overnight
  3. B1006: cut with XbaI and SpeI
  4. 4C5 backbone: cut with EcoRI, PstI
  • for two part ligations: use GFP or RFP from #1, terminator from #2 (2 ligations- one for GFP, one for RFP)
  • for 3a ligation: use GFP or RFP from #1, terminator from #3, 4C5 backbone from #4 (2 ligations- one for GFP, one for RFP)

Meeting with Rayka- suggestions for Friday's (tomorrow's) meeting:

  • include a brief review/overview of project for clarification
    • basic schematics of the two sides of the project
    • details of each, including the devices we plan to build
    • ligation schemes in visuals
    • for digital, analog: 1. overall plan 2. ligation scheme (home slide) 3. troubleshooting/challenges (including potential solutions)

suggestion for ligations: add ATP (is most likely to go bad in buffer) include plans for next week: minimum and ideal agenda again after lab stuff Twitter slide: change title to Gold Medal Requirements (add Facebook?) Lab Logistics: suggestions to collaborate in lab more efficiently

7/30 Friday

Laura's Notebook

9am iGEM meeting in attendance: team (Chris, Karina, Alex, Greg, Francisco, Laura), Christina, Ryan, Rayka, Anusuya, Graham Things to accomplish/address by next week:

  • potential names of circuits (Laura, Rayka)
  • flow cytometry: Does Scanford work for E. Coli? (Chris, Graham)
  • get ligations to work! (everyone)
    • make sure DNA concentration is high enough
    • when looking at gel to estimate concentration, look directly at gel (not at image on computer screen)
    • use fresh ligase buffer (or add ATP)
    • get successful ligation to use as positive control (from Ryan?)
  • get RSID1C PCR working
    • check concentration of primers: mix well, make new working stock
    • double check annealing temperatures, correct sequences
  • 4 piece PCR (Alex)- order as 2 pieces?
  • circuit diagrams, including levels of abstraction, consistent formats
  • Twitter:
    • list/group
    • record audio (in as many languages as possible)