User:Matt Hartings/Notebook/Photosynthesis/2013/01/31: Difference between revisions

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|style="background-color: #EEE"|[[Image:Hartings_AU_Photosynthesis_Lab_Header.png|128px]]<span style="font-size:22px;"> Protein Re-engineering</span>
|style="background-color: #EEE"|[[Image:Hartings_AU_Photosynthesis_Lab_Header.png|128px]]<span style="font-size:22px;"> Protein Re-engineering</span>
|style="background-color: #F2F2F2" align="center"|<html><img src="/images/9/94/Report.png" border="0" /></html> [[{{#sub:{{FULLPAGENAME}}|0|-11}}|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}|<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>[[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]]<html>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</html>}}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]]<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>}}
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==Objective==
==MOF==
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Abigail and I are trying a new MOF synthesis.  
51.8 mg DO2A
61.0 mg Zn(NO3)2 6H20
3 mL of diethylformamide


in a scint vial with a teflon cap
sonicate to create a suspension
Place in oven at 130C at 9:45am
Abigail and I checked the reaction at 12pm, the solution was brown. This is much different than the first time we performed the reaction, where there was a clear solution with a percipitate. We are going to let it run until 1 and then let it cool.
==Transformation==
# Make plates
## 2.5g LB
## 2.0g Agar
## 100mL water
## autoclave
## add 100uL of 100mg/ml ampicilin
## Pour plates
#


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Latest revision as of 22:24, 26 September 2017

Protein Re-engineering Main project page
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MOF

Abigail and I are trying a new MOF synthesis. 51.8 mg DO2A 61.0 mg Zn(NO3)2 6H20 3 mL of diethylformamide

in a scint vial with a teflon cap

sonicate to create a suspension

Place in oven at 130C at 9:45am

Abigail and I checked the reaction at 12pm, the solution was brown. This is much different than the first time we performed the reaction, where there was a clear solution with a percipitate. We are going to let it run until 1 and then let it cool.

Transformation

  1. Make plates
    1. 2.5g LB
    2. 2.0g Agar
    3. 100mL water
    4. autoclave
    5. add 100uL of 100mg/ml ampicilin
    6. Pour plates