IGEM:British Columbia/2009/Notebook/Biosensor Sensitivity/2009/06/11: Difference between revisions

From OpenWetWare
Jump to navigationJump to search
No edit summary
No edit summary
Line 14: Line 14:
* Used 50uL of Elution Buffer instead of 100uL as wanted as high of a concentration as possible as the number of cells is less then usual (was not inncubated as long as usual)
* Used 50uL of Elution Buffer instead of 100uL as wanted as high of a concentration as possible as the number of cells is less then usual (was not inncubated as long as usual)
* Eric started overnight cultures of all 4 plasmids in case we need to do another miniprep tommorow
* Eric started overnight cultures of all 4 plasmids in case we need to do another miniprep tommorow
==Ampicillin - New stocks testing==
# Made a new stock of Amp-100
## 20 mL sH2O + 2.0755 g ampicillin sodium salt
## Filter sterilized
# Stored in 2x 15 mL culture tubes (1000X stock)
# Tested by spread plating 20µL of stock


<!-- ## Do not edit below this line unless you know what you are doing. ## -->
<!-- ## Do not edit below this line unless you know what you are doing. ## -->

Revision as of 14:24, 7 August 2009

iGEM Project name 1 <html><img src="/images/9/94/Report.png" border="0" /></html> Main project page
<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>Previous entry<html>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</html>Next entry<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>

Miniprep of RBS-RFP-Terminator, Assembly 1 (J23100 + GFP), pBAD reverse and Amp/Tet Construction Plasmid

  • Day cultures of 5.6mL media and cells innoculated from plates were started at 10:50
  • RBS-RFP-Terminator, Assembly 1 and pBAD reverse were all grown using LB-Amp
  • Amp/Tet Construction Plasmid was grown on LB-Tet
  • Three cultures of Assembly 1 were started because the colonies on the plates did not have a noticible green flouresence
  • Miniprepped using a Invitrogen ChargeSwitch Pro Filter Plasmid Miniprep kit after 7 hours culture
  • Did not observe many cells after being spun down in a Galaxy 16 centrifuge
  • Used 50uL of Elution Buffer instead of 100uL as wanted as high of a concentration as possible as the number of cells is less then usual (was not inncubated as long as usual)
  • Eric started overnight cultures of all 4 plasmids in case we need to do another miniprep tommorow

Ampicillin - New stocks testing

  1. Made a new stock of Amp-100
    1. 20 mL sH2O + 2.0755 g ampicillin sodium salt
    2. Filter sterilized
  2. Stored in 2x 15 mL culture tubes (1000X stock)
  3. Tested by spread plating 20µL of stock