From 2008.igem.org
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| + | mZgAkl <a href="http://fbdnisdgysij.com/">fbdnisdgysij</a>, [url=http://jzowycxvfekb.com/]jzowycxvfekb[/url], [link=http://lkctxlgmquum.com/]lkctxlgmquum[/link], http://obyjjyzxsbxr.com/ |
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- | <!--PLACE TEXT BELOW HERE --> | + | |
- | == July 1, 2008 == | + | |
- | Made Yeast Media
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- | YPD Medium, per liter:
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- | 10g yeast extract
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- | 20g peptone
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- | 20g dextrose
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- | 20g agar(only for plates)
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- | 1. Dextrose filter sterilized, the rest autoclaved
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- | 2. Weigh nutrients into flask double the volume you want to make, and stir to dissolve
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- | 3. Dextrose added to autoclaved media to equivalent of 20 g/L
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- | 4. Liquid media placed on bench, plate media placed in 65 degree water bath approximately 5 minutes
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- | 5. Poured into plates and allowed to solidify
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- | == July 17, 2008 == | + | |
- | E.Coli Media
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- | LB medium, per liter
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- | 10g tryptone
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- | 5g yeast extract
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- | 5g NaCl
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- | 1 mL 1N NaOH
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- | 15g (agar for plates)
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- | 1. Antibody DNA resuspended in TE buffer, 0.1 μg/μL
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- | 2. 5mL LB inoculated with single colony DH5a pro
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- | 3. Incubated at 37 degrees overnight
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- | == July 18, 2008 ==
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- | Competent cells:
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- | 1. 3mL overnight culture of DH5a pro
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- | 2. Inoculated into 35mL of LB
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- | 3. OD600 checked, want 0.2-0.3
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- | 4. Place culture on ice for 3 minutes
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- | 5. Spin at 10,000 rpm for 7 minutes, discard supernatant
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- | 6. Resuspend in 10 mL cold 30 mM CaCl2, incubated on ice overnight
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- | <!-- == Insert Date Here ==
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- | * lab procedure
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- | ** more lab procedure
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- | * second lab procedure
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- | ** more about second lab procedure
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- | COPY/PASTE THEN REMOVE THIS AND BRACKETS-->
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- | {{bottom_template}}
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Latest revision as of 06:22, 29 March 2016
mZgAkl <a href="http://fbdnisdgysij.com/">fbdnisdgysij</a>, [url=http://jzowycxvfekb.com/]jzowycxvfekb[/url], [link=http://lkctxlgmquum.com/]lkctxlgmquum[/link], http://obyjjyzxsbxr.com/