Team:WashU/Protocols/EthanolExtraction

From 2012.igem.org

(Difference between revisions)
(Created page with "{{WashUback}} ==Caroteinoid Extraction using Ethanol== #Take the requisite volume of culture wanted for extraction. The more culture you use, the more cells you will have. Star...")
Line 1: Line 1:
{{WashUback}}
{{WashUback}}
-
==Caroteinoid Extraction using Ethanol==
+
==Caroteinoid Extraction==
#Take the requisite volume of culture wanted for extraction. The more culture you use, the more cells you will have. Start by taking 1 ml of culture and place it into an Eppendorf tube.  
#Take the requisite volume of culture wanted for extraction. The more culture you use, the more cells you will have. Start by taking 1 ml of culture and place it into an Eppendorf tube.  

Revision as of 14:49, 26 July 2012


Caroteinoid Extraction

  1. Take the requisite volume of culture wanted for extraction. The more culture you use, the more cells you will have. Start by taking 1 ml of culture and place it into an Eppendorf tube.
  2. Spin the culture down for 1 minute at 12,000 RPM
  3. Remove supernatant.
  4. Repeat steps 1 to 3 until you have pelleted the requisite amount of cells.
  5. Now, resuspend pelleted cells in .5 mL of ethanol. Spin for 1 minute at 12,000RPM.
  6. Save the supernatant, as it now contains the carotenoids. If the pellet is still colored, repeat step 5, saving the supernatant, until the pellet is white or until you are satisfied with the amount of carotenoids extracted.


Back to Protocols