Team:Stanford/Notebook/Lab Work/Week 4

From 2010.igem.org

(Difference between revisions)
(Christopher's iGEM Notebook)
Line 30: Line 30:
*for each plate, pick 8 colonies and streak, starting at the center of the "pie piece," and working towards the perimeter of the plate
*for each plate, pick 8 colonies and streak, starting at the center of the "pie piece," and working towards the perimeter of the plate
*plate ID's:
*plate ID's:
 +
 +
==7/14 Wednesday==
 +
===Laura's Notebook===
 +
*plates restreaked yesterday look good- bacteria grew well, some individual colonies
 +
*helped Francisco with minipreps (Promega kit) of : terminator, GFP, RFP
 +
**Francisco set up liquid cultures yesterday afternoon
 +
*Francisco poured, ran 0.8% gel
 +
**yesterday's digestions, with today's minipreps as controls
 +
*gel extraction: (I cut out bands, Francisco and Karina extracted)
 +
{|
 +
|part || tube mass (g) || tube + gel (g) || gel (g) || volume QG (uL)
 +
|-
 +
|terminator || 1.03 || 1.14 || 0.11 || 330
 +
|-
 +
|RFP || 1.11 || 1.18 || 0.07 || 210
 +
|-
 +
|GFP || 1.03 || 1.13 || 0.10 || 300
 +
|}
 +
 +
</div>
</div>

Revision as of 17:42, 20 July 2010

Quad center.jpg

Spring: Brainstorming | Spring Meetings

Summer: Week 1 | Week 2 | Week 3 | Week 4 | Week 5 | Week 6 | Week 7 | Week 8 | Week 9 | Week 10 | Summaries


Contents

7/12 Monday

Christopher's Notebook

  • Run Gel of Restricted Digested RBS+GFP+Terminators (I746908 partial)
  • Gel Extract
  • Run Gel of Gel Extracted Digest Products from Friday:
 3C5     E/P 2738 bp (buffer 3)
F2620   E/S (on pSB1A2) 1061 bp
  • I746908 E/P (on psb1A2) 2093 bp-can’t separate
  • B0034 X/P (on psb1A2) 12 bp-do NOT run on gel
  • J23100 E/S (on psb1A2) 35 bp-do NOT run on gel

7/13 Tuesday

Christopher's Notebook

  • Run Gels (0.8%) of Restriction Digests:
 1M, 2M, 2J (X/P)
 F2620 (E/S)
 3C5 (E/P)
 I0500 (E/S)

Note: for PCR of I746908: after first gel of PCR product, gel extract, and then do a restriction digest. After restriction digest, do a reaction cleanup; pieces are ready for ligation.

Laura's Notebook

  • restreaked plates from 7/1/10 (with Karina)
  • for each plate, pick 8 colonies and streak, starting at the center of the "pie piece," and working towards the perimeter of the plate
  • plate ID's:

7/14 Wednesday

Laura's Notebook

  • plates restreaked yesterday look good- bacteria grew well, some individual colonies
  • helped Francisco with minipreps (Promega kit) of : terminator, GFP, RFP
    • Francisco set up liquid cultures yesterday afternoon
  • Francisco poured, ran 0.8% gel
    • yesterday's digestions, with today's minipreps as controls
  • gel extraction: (I cut out bands, Francisco and Karina extracted)
part tube mass (g) tube + gel (g) gel (g) volume QG (uL)
terminator 1.03 1.14 0.11 330
RFP 1.11 1.18 0.07 210
GFP 1.03 1.13 0.10 300