840:153g:Projects/project25/2012/09/13

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(Autocreate 2012/09/13 Entry for 840:153g:Projects/project25)
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Team Members
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Tango-Alpha
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    Bess Lippmann
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    Colby Swanson
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    Name of student
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Cloning of mreB gene from ''Caulobacter crescentus'' into ''E. coli''. 
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    Name of student
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Project Name and Description
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9/11/12
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Tuesday, we updated and uploaded our project description and powerpoint presentation.  We also prepared and ordered (through our instructor) our first primer sets, the extended (with biobricks) primers as seen in our powerpoint and primers without biobricks as a back up.
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    Explain your experimental design here
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9/13/12
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    List all the steps that are needed to complete your project
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Today was spent mostly on preparations:
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    Do not go into experimental details and don't list procedures. Just list the major steps necessary to complete your project
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-Making PYE media for ''C. crescentus''
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    Please also make yourself familiar with uploading pictures and *.ppt files
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-Making Reagants for our bacterial genome DNA extraction
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Important Results and Milestones
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    keep track of your most important results and refer to the corresponding page in your notebook
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    upload important pictures (don't forget to label them! Powerpoint is very convenient). Remember: these will become quite handy later in your summary report or final presentation. If you do label and upload the pictures as soon as you got them, your summary report can be written much more effortlessly (do you usually procrastinate? This is chance to do some work before hand that frees you up for finals week).
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Recent changes
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Revision as of 17:31, 13 September 2012

Tango-Alpha

   Bess Lippmann
   Colby Swanson 

Cloning of mreB gene from Caulobacter crescentus into E. coli.

9/11/12 Tuesday, we updated and uploaded our project description and powerpoint presentation. We also prepared and ordered (through our instructor) our first primer sets, the extended (with biobricks) primers as seen in our powerpoint and primers without biobricks as a back up.

9/13/12 Today was spent mostly on preparations: -Making PYE media for C. crescentus -Making Reagants for our bacterial genome DNA extraction

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