Team:Northwestern/makecells

From 2013.igem.org

(Difference between revisions)
(Created page with "{{:Team:Northwestern/Templates/Skinning}} <html> <style> p { color:black; font-family: helvetica; } .container { display: inline-block; background-color: #C3...")
 
Line 175: Line 175:
</style>  
</style>  
-
<div class = "container">
 
-
<div class = "menu">
 
-
<ul>
 
-
<li><a href="https://2013.igem.org/Team:Northwestern">Home</a></li>
 
-
<li><a href="https://2013.igem.org/Team:Northwestern/Team">Team</a>
 
-
<ul>
 
-
<li><a href="https://igem.org/Team.cgi?year=2013&team_name=Northwestern">Official Profile</a></li>
 
-
<li><a href="#">Meet Us!</a></li>
 
-
<li><a href="https://2013.igem.org/Team:Northwestern/Attributions">Attribution</a></li>
 
-
</ul>
 
-
</li>
 
-
<li><a href="https://2013.igem.org/Team:Northwestern/Project">Project</a>
 
-
<ul>
 
-
<li><a href="https://2013.igem.org/Team:Northwestern/Parts">Parts Submitted</a></li>
 
-
<li><a href="https://2013.igem.org/Team:Northwestern/Notebook">Notebook</a></li>
 
-
<li><a href="#">Description</a></li>
 
-
</ul>
 
-
</li>
 
-
<li><a href="https://2013.igem.org/Team:Northwestern/Modeling">Modeling</a></li>
 
-
<li><a href= "https://2013.igem.org/Team:Northwestern/Safety"> Safety </a></li>
 
-
</ul>
 
-
</div>
 
-
</div>
 
<div>
<div>

Latest revision as of 00:37, 28 September 2013

Making Competent Cells

Create Needed Solutions

  • SOB
  • CCMB80 (Ion Solution)

Grow Cells Overnight

  • Start with Top 10 Cells (from Culture) and grow (Take single colony from plate, and swirl in ~5mL of SOB in overnight tube)
  • Grow the Cells in shaker (200rpm @ 37C) for ~16 hours
  • Measuring Optical Density

    Preparing Solutio

    • Aliquot 100mL of SOB into an Erlenmeyer Flask
    • Add .5mL of 2M magnesium chloride (MgCl2)
    • Autoclave
    • Rinse flask with water for ~1minute to cool
    • Add 1mL of overnight SOB + cell solution
    • Put into shaker (200rpm @ 37C) for 2 hours

    Preparing the Spectrophotometer

    • Turn on the spectrophotometer
    • When ready to measure optical density, blank with regular SOB solution
    • Get cuvettes ready

    Measuring the Optical Density

    • At 2 hours measure the OD
    • Continue to measure the OD every 20-30 minutes until it reaches .35
    • Note: This growth is exponential, so be quick if close to .35
    • If it exceeds .4, discard solution and start over

    Centrifuging the Cells

    • When the solution has an OD between .35 and .4
    • Split into chilled 50mL centrifuge tubes and put on ice for 10 minutes (Have centrifuge tubes chilled in -20C freezer before-hand)
    • Centrifuge for 10 minutes (4000rpm @ 4C) (Make sure to have a pellet at the bottom of the tube)
    • Decant the supernatant and leave upside down on paper towel for a minute
    • Resuspend the pellet in 30mL of CCMB80 solution
      • Have the CCMB80 solution ice cold before this
      • Gently do this by swishing up and down in transfer pipet
      • This may take upwards of 10 minutes, be patient
    • Decant the supernatant and leave upside down on paper towel for a minute
    • Resuspend the pellet in 2mL of CCMB80 solution (Add the solution and just shake the tube to resuspend)

    Putting the Cells on Ice

    • Aliquot the total solution into microcentrifuge tubes (Try to break it up into smaller amounts in many microcentrifuge tubes)
    • Place the microcentrifuge tubes into the -80C freezer for later use