User:Matt Hartings/Notebook/Photosynthesis/2012/02/08: Difference between revisions
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This | This procedure was continued [[User:Matt_Hartings/Notebook/Photosynthesis/2012/02/10|here]] | ||
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Revision as of 10:02, 13 February 2012
 Biomaterials Design Lab
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ObjectiveExpression of K31C Ascaris Hemoglobin in BL21 (DE3) cells. Description(7:45am) I centrifuged the starter cultures from the previous evening (4x25ml for 15 minutes at 4500rpm and 4C). I added 1ml each of ampicilin (100mg/ml) and hemin (40mg/ml in dimethylformamide) to each 1L of expression media. I resuspended all 4 pellets in 4 mL of fresh LB broth and redistributed the pellets to each of the 1L of expression media. Because the OD(600) can't be accurately measured do to the presence of hemin, I have to estimate when is the right time to induce expression. (12:00pm) I added 1mL of IPTG (0.4g in 4mL) to each expression flask to induce expression. (3:00pm) Along with Paul, I centrifuged the expression cultures to isolate the cells (4x500mL for 15 minutes at 4500 rpm and 4C - This procedure was carried out twice). After centrifugation we resuspended the cell pellets in 50mM tris 50mM NaCl pH8. (35 mL was used to resuspend the cells from 2 of the centrifuge tubes. This was done twice). The cells were placed at -80C overnight. Data
NotesThis procedure was continued here
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