Difference between revisions of "Team:UCLA/Notebook/Honeybee Silk/21 May 2015"
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+ | |||
+ | <!-- Start of menu --> | ||
+ | <div id="menuContainer"> | ||
+ | |||
+ | <!-- This list is your menu, every list item is a menu button and nested listed become submenu buttons --> | ||
+ | <ul> | ||
+ | <a href="https://2015.igem.org/Team:UCLA"><li>HOME</li></a> | ||
+ | |||
+ | <a href="https://2015.igem.org/Team:UCLA/Team"><li>TEAM</li></a> | ||
+ | |||
+ | <a href="#"><li>PROJECTS | ||
+ | <ul> | ||
+ | <!-- <a href="https://2015.igem.org/Team:UCLA/Description"><li>Description</li></a> | ||
+ | <a href="https://2015.igem.org/Team:UCLA/Experiments"><li>Experiments & Protocols</li></a> | ||
+ | <a href="https://2015.igem.org/Team:UCLA/Results"><li>Results</li></a> | ||
+ | <a href="https://2015.igem.org/Team:UCLA/Design"><li>Design</li></a>--> | ||
+ | <a href="https://2015.igem.org/Team:UCLA/Projects/Silks"><li>Silk Genetics</li></a> | ||
+ | <a href="https://2015.igem.org/Team:UCLA/Projects/Functionalization"><li>Functionalization</li></a> | ||
+ | <a href="https://2015.igem.org/Team:UCLA/Projects/Materials"><li>Materials Processing</li></a> | ||
+ | <a href="https://2015.igem.org/Team:UCLA/Projects/Protein_Cages"><li>Protein Cages</li></a> | ||
+ | </ul> | ||
+ | </li></a> | ||
+ | |||
+ | <a href="#"><li>PARTS | ||
+ | <ul> | ||
+ | <a href="https://2015.igem.org/Team:UCLA/Parts"><li>Team Parts</li></a> | ||
+ | <a href="https://2015.igem.org/Team:UCLA/Basic_Part"><li>Basic Parts</li></a> | ||
+ | <a href="https://2015.igem.org/Team:UCLA/Composite_Part"><li>Composite Parts</li></a> | ||
+ | <a href="https://2015.igem.org/Team:UCLA/Part_Collection"><li>Part Collection</li></a> | ||
+ | </ul> | ||
+ | </li></a> | ||
+ | |||
+ | <a href="https://2015.igem.org/Team:UCLA/Notebook"><li>NOTEBOOKS | ||
+ | <ul> | ||
+ | <a href="https://2015.igem.org/Team:UCLA/Notebook/Spider_Silk_Genetics"><li>Spider Silk Genetics</li></a> | ||
+ | <a href="https://2015.igem.org/Team:UCLA/Notebook/Honeybee_Silk"><li>Honeybee Silk</li></a> | ||
+ | <a href="https://2015.igem.org/Team:UCLA/Notebook/Recombinant_Expression"><li>Recombinant Silk Functionalization</li></a> | ||
+ | <a href="https://2015.igem.org/Team:UCLA/Notebook/Materials"><li>Materials Processing</li></a> | ||
+ | <a href="https://2015.igem.org/Team:UCLA/Notebook/Protein_Cages"><li>Protein Cages</li></a> | ||
+ | <a href="https://2015.igem.org/Team:UCLA/Notebook/Interlab_Study"><li>UCLA Measurement Interlab Study</li></a> | ||
+ | </ul> | ||
+ | </li></a> | ||
+ | |||
+ | <a href="#"><li>MEETING NOTES | ||
+ | <ul> | ||
+ | <a href="https://2015.igem.org/Team:UCLA/Notebook/General_Meetings"><li>General Meetings</li></a> | ||
+ | <a href="https://2015.igem.org/Team:UCLA/Notebook/Coordinator_Meetings"><li>Coordinator Meetings</li></a> | ||
+ | <a href="https://2015.igem.org/Team:UCLA/Notebook/Advisor_Meetings"><li>Advisor Meetings</li></a> | ||
+ | </ul> | ||
+ | </li></a> | ||
+ | |||
+ | |||
+ | <a href="https://2015.igem.org/Team:UCLA/Attributions"><li>ATTRIBUTIONS</li></a> | ||
+ | |||
+ | <a href="https://2015.igem.org/Team:UCLA/Collaborations"><li>COLLABORATIONS</li></a> | ||
+ | |||
+ | <a href="https://2015.igem.org/Team:UCLA/Practices"><li>HUMAN PRACTICES</li></a> | ||
+ | |||
+ | <a href="https://2015.igem.org/Team:UCLA/Safety"><li>SAFETY</li></a> | ||
+ | |||
+ | <a href="https://2015.igem.org/Team:UCLA/Modeling"><li>MODELING</li></a> | ||
+ | |||
+ | <a href="https://2015.igem.org/Team:UCLA/Measurement"><li>MEASUREMENT STUDY</li></a> | ||
+ | |||
+ | <a href="https://2015.igem.org/Team:UCLA/Software"><li>SOFTWARE</li></a> | ||
+ | |||
+ | <a href="https://2015.igem.org/Team:UCLA/Entrepreneurship"><li>ENTREPRENEURSHIP</li></a> | ||
+ | |||
+ | </ul> | ||
+ | </div> | ||
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+ | |||
+ | <!-- Start of content --> | ||
+ | <div id="contentContainer"> <!--The closing tag for contentContainer should be placed at the bottom of each content page.--> | ||
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+ | |||
+ | ='''Inoculation of 5/19 Transformation'''= | ||
+ | |||
+ | *I picked four colonies from the 1:1 kanamycin plate and suspended each in 100uL ddH2O | ||
+ | *Each sample was inoculated in 3 different culture tubes with 5mL LB broth and 5uL 1000X kanamycin and was incubated at 37C. |
Latest revision as of 21:15, 10 July 2015
Inoculation of 5/19 Transformation
- I picked four colonies from the 1:1 kanamycin plate and suspended each in 100uL ddH2O
- Each sample was inoculated in 3 different culture tubes with 5mL LB broth and 5uL 1000X kanamycin and was incubated at 37C.