User:NYOUSHA Yousefi/Notebook/Protein Engineering/2013/01/29: Difference between revisions
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|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;"> Project name</span> | |style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;"> Project name</span> | ||
|style="background-color: #F2F2F2" align="center"| | |style="background-color: #F2F2F2" align="center"|[[File:Report.png|frameless|link={{#sub:{{FULLPAGENAME}}|0|-11}}]][[{{#sub:{{FULLPAGENAME}}|0|-11}}|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}|[[File:Resultset_previous.png|frameless|link={{#lnpreventry:{{FULLPAGENAME}}}}]][[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]] }}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]][[File:Resultset_next.png|frameless|link={{#lnnextentry:{{FULLPAGENAME}}}}]]}} | ||
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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== | ||
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# 5ul of Ampicillin was added to both test tubes | # 5ul of Ampicillin was added to both test tubes | ||
# The frozen cells of PQE-80 bacteria in glycerol were taken out of the -80 degree C fridge | # The frozen cells of PQE-80 bacteria in glycerol were taken out of the -80 degree C fridge | ||
# Some PQE-80 bacteria cells were added to these LB | # Some PQE-80 bacteria cells were added to these LB mediums under sterile conditions | ||
# PQE-80 bacteria were also added to four erlyn meyer flasks containing LB media and 35ul Ampicillin | # PQE-80 bacteria were also added to four erlyn meyer flasks containing LB media and 35ul Ampicillin | ||
# The tubes and flasks were placed in the incubator/shaker at 37 degree C for 24h | # The tubes and flasks were placed in the incubator/shaker at 37 degree C for 24h |
Latest revision as of 22:24, 26 September 2017
Project name | Main project page Previous entry Next entry |
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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