Difference between revisions of "SDS Page-Gel for all the bovine proteins"

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Participants: Wesley, Meenakshi, Nikola, Johan
Participants: Wesley, Meenakshi, Nikola, Johan


Materials:  
Materials: casein, 3B(100 fold diluted), 6B (100 fold diluted), 7 (100 fold diluted), 2B (100 fold diluted), control SFOA, transformed negative control, liquid culture, Bovine Beta B (8) - 20ml + 4ml loading dye, Bovine Alpha A (8) - 20ml + 4ml loading dye


Method:
Method:  
Get 3 colonies from each plates in 1 centrifuge tube + resuspend into 20ml distilled water
For casein touch 1 20-2w microliter pipette tip and rinse with 20 microliter dionised water in 1 casein control tube
One sample take 1 colony from SFOA (as a negative control)
One sample from control yeast transform plate


To run the gel
Take 20 microliter of sample and 4 microliter loading dye
Boil all the samples for 10 minutes
Put  400ml loading buffer in tank.
(We have  , so, 10ml in 90 ml distilled water.)


Result:
Result:

Revision as of 06:18, 25 November 2014

SDS Page-Gel for all of the bovine proteins

Monday Nov 24th

SDS Page-Gel for all of the bovine proteins

Participants: Wesley, Meenakshi, Nikola, Johan

Materials: casein, 3B(100 fold diluted), 6B (100 fold diluted), 7 (100 fold diluted), 2B (100 fold diluted), control SFOA, transformed negative control, liquid culture, Bovine Beta B (8) - 20ml + 4ml loading dye, Bovine Alpha A (8) - 20ml + 4ml loading dye

Method: Get 3 colonies from each plates in 1 centrifuge tube + resuspend into 20ml distilled water For casein touch 1 20-2w microliter pipette tip and rinse with 20 microliter dionised water in 1 casein control tube One sample take 1 colony from SFOA (as a negative control) One sample from control yeast transform plate

To run the gel Take 20 microliter of sample and 4 microliter loading dye Boil all the samples for 10 minutes Put 400ml loading buffer in tank. (We have , so, 10ml in 90 ml distilled water.)


Result: