User:NYOUSHA Yousefi/Notebook/Protein Engineering/2013/01/29: Difference between revisions
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==Procedure 1== | ==Procedure 1== | ||
# 0.2g D-manitol was added to four set of | # 0.2g D-manitol was added to four set of tubes and 0.2g P-sorbitol was added to another set of four tubes, each tube recieved 0.2g of sugar | ||
# 0.1g of Polyethylene Glycol (PEG), M.W. 20,000 was added to all tubes | # 0.1g of Polyethylene Glycol (PEG), M.W. 20,000 was added to all tubes | ||
# 10ml of four set of buffers including phosphate, tris, citrate, and acetate were added to tubes in an order that each four set of tubes received only one of these buffers | # 10ml of four set of buffers including phosphate, tris, citrate, and acetate were added to tubes in an order that each four set of tubes received only one of these buffers | ||
# The tubes were vortexed to dissolve PEG into the buffer and sugar solution | # The tubes were vortexed to dissolve PEG into the buffer and sugar solution | ||
# Finally the tubes were placed in -80 degree C to freeze and then they were placed in the vacuum for lyophilization | # Finally, the tubes were placed in -80 degree C nitrogen to freeze and then they were placed in the vacuum for lyophilization | ||
==Objective 2== | ==Objective 2== |
Revision as of 06:58, 5 February 2013
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Entry titlePreparing protein solutions and lyophilization Objective 1Eight different protein solutions were prepared for lyophilization Procedure 1
Objective 2Culturing PQE-80 antibiotic resistant bacteria Procedure 2
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