Team:Lethbridge Canada/notebook may

From 2013hs.igem.org

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<ul>
<ul>
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/project">Description</a></li>
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/project">Description</a></li>
 +
                                                <li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/project#video_oxy">Visual Modeling</a></li>
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/math">Math Model</a></li>
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/math">Math Model</a></li>
 +
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/results">Results</a></li>
 +
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/wikifreeze">Wikifreeze</a></li>
</ul>
</ul>
</li>
</li>
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<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/notebook_april">Notebook: April</a></li>
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/notebook_april">Notebook: April</a></li>
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/notebook_may">Notebook: May</a></li>
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/notebook_may">Notebook: May</a></li>
 +
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/notebook_june">Notebook: June</a></li>
</ul>
</ul>
</li>
</li>
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<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/videos">Videos</a></li>
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/videos">Videos</a></li>
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/surveys">Parent Surveys</a></li>
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/surveys">Parent Surveys</a></li>
 +
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/novel_study">Novel Study</a></li>
</ul>
</ul>
</li>
</li>
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<div id="notebook_header">
<div id="notebook_header">
<div id="notebook_links">
<div id="notebook_links">
-
<h1 id="notebook_links_header">Notebook Links</h1>
+
 +
<h1 id="notebook_links_header"> Notebook Links</h1>
 +
 
<ul id="notebook_march_links">
<ul id="notebook_march_links">
<li class="notebook_link_title"><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/notebook_march">March</a></li>
<li class="notebook_link_title"><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/notebook_march">March</a></li>
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<ul id="notebook_june_links">
<ul id="notebook_june_links">
-
<li class="notebook_link_title"><a href="notebook_june.html">June</a></li>
+
<li class="notebook_link_title"><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/notebook_june">June</a></li>
-
<li><a href="notebook_june.html#entry_one">June 1, 2013: Restrictions</a></li>
+
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/notebook_june#entry_one">June 1, 2013: Restrictions</a></li>
-
<li><a href="notebook_june.html#entry_two">June 2, 2013: Transformation</a></li>
+
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/notebook_june#entry_two">June 2, 2013: Transformation</a></li>
-
<li><a href="notebook_june.html#entry_three">June 4, 2013: Picked Colonies</a></li>
+
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/notebook_june#entry_three">June 4, 2013: Picked Colonies</a></li>
-
<li><a href="notebook_june.html#entry_four">June 10, 2013: Sent constructs for sequencing</a></li>
+
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/notebook_june#entry_four">June 10, 2013: Sent constructs for sequencing</a></li>
-
<li><a href="notebook_june.html#entry_five">Transformation of OXY into BL21</a></li>
+
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/notebook_june#entry_five">June 13, 2013: Transformation of OXY into BL21</a></li>
-
<li><a href="notebook_june.html#entry_six">Restricted and Ligated and Transformed</a></li>
+
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/notebook_june#entry_six">June 13, 2013: Restricted and Ligated and Transformed</a></li>
-
<li><a href="notebook_june.html#entry_seven">Picked Cells</a></li>
+
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/notebook_june#entry_seven">June 13, 2013: Picked Cells</a></li>
 +
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/notebook_june#entry_eight">June 15, 2013: Ni-Sepharose Purification</a></li>
 +
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/notebook_june#entry_nine">June 18, 2013: Tris-Tricine PAGE</a></li>
 +
<li><a href="https://2013hs.igem.org/Team:Lethbridge_Canada/notebook_june#entry_ten">June 21, 2013: Anti-His Slot Blot</a></li>
</ul>
</ul>
</div>
</div>
</div>
</div>
-
 
+
<div class="pull_banner_left">
 +
<img src="https://static.igem.org/mediawiki/2013hs/7/75/Lethbridge_hs_igem_2013_banner_notebookmay.png">
 +
</div>
<div id="notebook_body">
<div id="notebook_body">
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<h1 class="notebook_entry_header">Ligations</h1>
<h1 class="notebook_entry_header">Ligations</h1>
<ul class="notebook_entry_list">
<ul class="notebook_entry_list">
-
<li>Name: Yoyo Yao</li>
+
<li>Name: Yoyo Y</li>
<li>Date: May 1, 2013</li>
<li>Date: May 1, 2013</li>
<li class="notebook_nested_start">Ligation of Parts – Upstream, Ligated at sites S & P:  
<li class="notebook_nested_start">Ligation of Parts – Upstream, Ligated at sites S & P:  
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<div class="restrict_width">
<div class="restrict_width">
<ul class="notebook_entry_list">
<ul class="notebook_entry_list">
-
<li>Name: Mackenzie</li>
+
<li>Name: Mackenzie C</li>
<li>Date: May 4, 2013</li>
<li>Date: May 4, 2013</li>
<li>35µL DNA, 14µL MM, 0.5µL Spe1, 0.5µL Pst1</li>
<li>35µL DNA, 14µL MM, 0.5µL Spe1, 0.5µL Pst1</li>
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<h1 class="notebook_entry_header">1% Agarose Gel of Promoter Constructs</h1>
<h1 class="notebook_entry_header">1% Agarose Gel of Promoter Constructs</h1>
<ul class="notebook_entry_list">
<ul class="notebook_entry_list">
-
<li>Name: Mackenzie</li>
+
<li>Name: Mackenzie C</li>
<li>Date: May 4, 2013</li>
<li>Date: May 4, 2013</li>
</ul>
</ul>
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<ul class="notebook_entry_list">
<ul class="notebook_entry_list">
<li>Date: May 4, 2013</li>
<li>Date: May 4, 2013</li>
-
<li>J23108 J61002</li>
+
<li>J23108_J61002</li>
-
<li>J23113 J61002</li>
+
<li>J23113_J61002</li>
-
<li>J23114 J61002</li>
+
<li>J23114_J61002</li>
-
<li>J23100 J61002</li>
+
<li>J23100_J61002</li>
<li>Eluted 50 µL</li>
<li>Eluted 50 µL</li>
</ul>
</ul>
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<div class="restrict_width_small">
<div class="restrict_width_small">
<ul class="notebook_entry_list">
<ul class="notebook_entry_list">
-
<li>Name: Mackenzie</li>
+
<li>Name: Mackenzie C</li>
<li>Date: May 5, 2013</li>
<li>Date: May 5, 2013</li>
</ul>
</ul>
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<h1 class="notebook_entry_header">Restriction</h1>
<h1 class="notebook_entry_header">Restriction</h1>
<ul class="notebook_entry_list">
<ul class="notebook_entry_list">
-
<li>Name: Chris Isaac</li>
+
<li>Name: Chris I</li>
<li>Date: May 7, 2013</li>
<li>Date: May 7, 2013</li>
<li>Cut with ‘X’ and ‘P’</li>
<li>Cut with ‘X’ and ‘P’</li>
-
<li>J06702 – RBS-mcherry-DT</li>
+
<li>J06702–RBS-mCherry-DT</li>
</ul>
</ul>
<p class="top_notebook"><a href="#wrapper">Back to Top</a></p>
<p class="top_notebook"><a href="#wrapper">Back to Top</a></p>
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<h1 class="notebook_entry_header">Gel Extraction</h1>
<h1 class="notebook_entry_header">Gel Extraction</h1>
<ul class="notebook_entry_list">
<ul class="notebook_entry_list">
-
<li>Name: Katie T. & Elaine B.</li>
+
<li>Name: Katie T, Elaine B</li>
<li>Date: May 7, 2013</li>
<li>Date: May 7, 2013</li>
<li>J06702</li>
<li>J06702</li>
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<h1 class="notebook_entry_header">Gel Extraction</h1>
<h1 class="notebook_entry_header">Gel Extraction</h1>
<ul class="notebook_entry_list">
<ul class="notebook_entry_list">
-
<li>Name: Carissa K.</li>
+
<li>Name: Carissa K</li>
<li>Date: May 8, 2013</li>
<li>Date: May 8, 2013</li>
-
<li>2ul of J06702 mix with 4ul of each; J23100, J23108, J23113, J23114 all in plasmid J61002 (amp)</li>
+
<li>2µL of J06702 mix with 4µL of each; J23100, J23108, J23113, J23114 all in plasmid J61002 (amp)</li>
-
<li>In the Thermo-cycler at 16 degrees Celsius overnight followed by heat kill.</li>
+
<li>In the Thermo-cycler at 16°C overnight followed by heat kill.</li>
</ul>
</ul>
<p class="top_notebook"><a href="#wrapper">Back to Top</a></p>
<p class="top_notebook"><a href="#wrapper">Back to Top</a></p>
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<h1 class="notebook_entry_header">PCR of Ligation Mixture(PCR to verify insert in clone vector)</h1>
<h1 class="notebook_entry_header">PCR of Ligation Mixture(PCR to verify insert in clone vector)</h1>
<ul class="notebook_entry_list">
<ul class="notebook_entry_list">
-
<li>Name: Chris Isaac</li>
+
<li>Name: Chris I</li>
<li>Date: May 9, 2013</li>
<li>Date: May 9, 2013</li>
<li>X7 Master Mix, Taq polymerase</li>
<li>X7 Master Mix, Taq polymerase</li>
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<h1 class="notebook_entry_header">Restriction of PCR Ligations Gel Conformation</h1>
<h1 class="notebook_entry_header">Restriction of PCR Ligations Gel Conformation</h1>
<ul class="notebook_entry_list">
<ul class="notebook_entry_list">
-
<li>Name: Patrick O'</li>
+
<li>Name: Patrick O</li>
<li>Date: May 13, 2013</li>
<li>Date: May 13, 2013</li>
-
<li>Restriction of May 9th pcr ligation at E and P and ran on 1.0% Gel (refreshed ETH Bromide)</li>
+
<li>Restriction of May 9th PCR ligation at E and P and ran on 1.0% Gel (refreshed ETH Bromide)</li>
<li>Ladder lane 2</li>
<li>Ladder lane 2</li>
<li>2space</li>
<li>2space</li>
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<li>J23114_J61002_J06702</li>
<li>J23114_J61002_J06702</li>
<li>Ladder</li>
<li>Ladder</li>
-
<li>Conclusion: Ligations were not Successful</li>
+
<li>Conclusion: Ligations were not successful</li>
<li><img src="https://static.igem.org/mediawiki/2013hs/7/7f/Lethbridge_hs_igem_2013_Gel-extraction-05-13-2013.gif" alt="Restriction of PCR Ligations Gel Conformation Image" /></li>
<li><img src="https://static.igem.org/mediawiki/2013hs/7/7f/Lethbridge_hs_igem_2013_Gel-extraction-05-13-2013.gif" alt="Restriction of PCR Ligations Gel Conformation Image" /></li>
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<li>Date: May 14, 2013</li>
<li>Date: May 14, 2013</li>
<li>Transformed ligation of J06702 with various promoters in plasmid J61002 : J23100, J23108, J23113, J23114 From May 8, 2013.</li>
<li>Transformed ligation of J06702 with various promoters in plasmid J61002 : J23100, J23108, J23113, J23114 From May 8, 2013.</li>
-
<li>Transformed 3ul ligation mix into 30ul of Dh5 alpha competent cells, used puc19 control. Heat shocked for 30second at 42 degrees Celsius added 200ul warm LB, incubated at 37 for 1 hour, Plated 100ul on amp LB Agar plates. Overnight at 37degrees Celsius.</li>
+
<li>Transformed 3µL ligation mix into 30µL of DH5α competent cells, used puc19 control. Heat shocked for 30 seconds at 42°C, added 200µL warm LB, incubated at 37°C for 1 hour. Plated 100µL on amp LB Agar plates. Incubated overnight at 37°C.</li>
</ul>
</ul>
<p class="top_notebook"><a href="#wrapper">Back to Top</a></p>
<p class="top_notebook"><a href="#wrapper">Back to Top</a></p>
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<h1 class="notebook_entry_header">Ligation Round 2 of May 14th Gel Extracted Parts</h1>
<h1 class="notebook_entry_header">Ligation Round 2 of May 14th Gel Extracted Parts</h1>
<ul class="notebook_entry_list">
<ul class="notebook_entry_list">
-
<li>11ul dh20</li>
+
<li>11µL dh20</li>
-
<li>2ul t4 dna ligase buffer</li>
+
<li>2µL t4 DNA ligase buffer</li>
-
<li>4ul DNA J06702</li>
+
<li>4µL DNA J06702</li>
-
<li>2ul DNA J23100, J23108, J23113, J23114 in plasmid J61002</li>
+
<li>2µL DNA J23100, J23108, J23113, J23114 in plasmid J61002</li>
-
<li>1ul T4 dna Ligase</li>
+
<li>1µL T4 DNA Ligase</li>
-
<li>Into the Thermo-cycler overnight at 16 degrees Celsius.</li>
+
<li>Into the Thermo-cycler overnight at 16°C.</li>
</ul>
</ul>
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<h1 class="notebook_entry_header">Picking Cells</h1>
<h1 class="notebook_entry_header">Picking Cells</h1>
<ul class="notebook_entry_list">
<ul class="notebook_entry_list">
-
<li>Name: Yoyo, Amrinder, Patrick, Orion</li>
+
<li>Name: Yoyo Y, Amrinder G, Patrick O, Orion S</li>
<li>Date: May 15, 2013</li>
<li>Date: May 15, 2013</li>
<li>Put 50µL of Amp resistance into 50mL of Lb media</li>
<li>Put 50µL of Amp resistance into 50mL of Lb media</li>
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<li>J23113_J61002</li>
<li>J23113_J61002</li>
<li>J23114_J61002</li>
<li>J23114_J61002</li>
-
<li>J06702_psb1ak2</li>
+
<li>J06702_pSB1AK2</li>
</ul>
</ul>
</li>
</li>
-
<li>Inserted tips of E. Coli into each flask</li>
+
<li>Inserted tips of E. coli into each flask</li>
</ul>
</ul>
<p class="top_notebook"><a href="#wrapper">Back to Top</a></p>
<p class="top_notebook"><a href="#wrapper">Back to Top</a></p>
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<h1 class="notebook_entry_header">Picking Cells</h1>
<h1 class="notebook_entry_header">Picking Cells</h1>
<ul class="notebook_entry_list">
<ul class="notebook_entry_list">
-
<li>Name: Amrinder, Orion</li>
+
<li>Name: Amrinder G, Orion S</li>
<li>Date: May 16, 2013</li>
<li>Date: May 16, 2013</li>
<li>Put 5µL of Amp into 5mL of Lb media</li>
<li>Put 5µL of Amp into 5mL of Lb media</li>
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<li>J23113_J61002</li>
<li>J23113_J61002</li>
<li>J23114_J61002</li>
<li>J23114_J61002</li>
-
<li>J06702_psb1ak2</li>
+
<li>J06702_pSB1AK2</li>
</ul>
</ul>
</li>
</li>
-
<li>Inserted tips of E. Coli into each tube</li>
+
<li>Inserted tips of E. coli into each tube</li>
</ul>
</ul>
<p class="top_notebook"><a href="#wrapper">Back to Top</a></p>
<p class="top_notebook"><a href="#wrapper">Back to Top</a></p>
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<li>Date: May 16, 2013</li>
<li>Date: May 16, 2013</li>
<li>Spun down 50ml of culture in falcon tubes</li>
<li>Spun down 50ml of culture in falcon tubes</li>
-
<li>5000xg twice for 2mins to collect cells</li>
+
<li>5000xg twice for 2 mins to collect cells</li>
-
<li>Resupended in 1ml solution1 2ml solution 2 and 3,5ml solution 3</li>
+
<li>Resupended in 1ml solution1 2ml solution 2 and 3, 5ml solution 3</li>
-
<li>Spun down at 6000xg for 6minutes to pellet cell debries</li>
+
<li>Spun down at 6000xg for 6 minutes to pellet cell debris</li>
-
<li class="notebook_nested_start">Eluted into 4 miniprep spin collumns twice to reach maximum binding effeciency<li>
+
<li class="notebook_nested_start">Eluted into 4 miniprep spin columns twice to reach maximum binding efficiency<li>
<li>
<li>
<ul class="notebook_nested_list">
<ul class="notebook_nested_list">
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<li>J23113_J61002</li>
<li>J23113_J61002</li>
<li>J23114_J61002</li>
<li>J23114_J61002</li>
-
<li>J06702_PSB1AK2</li>
+
<li>J06702_pSB1AK2</li>
</ul>
</ul>
</li>
</li>
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<div class="restrict_width">
<div class="restrict_width">
<ul class="notebook_entry_list">
<ul class="notebook_entry_list">
-
<li>Name: Krista Fjordbotten, Yoyo Yao</li>
+
<li>Name: Krista F, Yoyo Y</li>
<li>Date: May 17, 2013</li>
<li>Date: May 17, 2013</li>
<li class="notebook_nested_start">Restriction of:</li>
<li class="notebook_nested_start">Restriction of:</li>
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<li class="notebook_second_nested">J23113_J06702 J61002</li>
<li class="notebook_second_nested">J23113_J06702 J61002</li>
<li class="notebook_second_nested">J23114_J06702 J61002</li>
<li class="notebook_second_nested">J23114_J06702 J61002</li>
-
<li class="notebook_second_nested">J06702 J61002</li>
+
<li class="notebook_second_nested">J06702_J61002</li>
</ul>
</ul>
</li>
</li>
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<h1 class="notebook_entry_header">Miniprep</h1>
<h1 class="notebook_entry_header">Miniprep</h1>
<ul class="notebook_entry_list">
<ul class="notebook_entry_list">
-
<li>Name: Amrinder Grewal , Krista Fjordbotten</li>
+
<li>Name: Amrinder G, Krista F</li>
<li>Date: May 17, 2013</li>
<li>Date: May 17, 2013</li>
<li class="notebook_nested_start">Mini prep of (35µL EB):</li>
<li class="notebook_nested_start">Mini prep of (35µL EB):</li>
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</ul>
</ul>
</li>
</li>
-
<li>Inserted tips of E. Coli into each flask</li>
+
<li>Inserted tips of E. coli into each flask</li>
</ul>
</ul>
<p class="top_notebook"><a href="#wrapper">Back to Top</a></p>
<p class="top_notebook"><a href="#wrapper">Back to Top</a></p>
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<h1 class="notebook_entry_header">Glycerol Stock</h1>
<h1 class="notebook_entry_header">Glycerol Stock</h1>
<ul class="notebook_entry_list">
<ul class="notebook_entry_list">
-
<li>Name: Amrinder Grewal , Krista Fjordbotten, Yoyo Yao, Isaac Ward</li>
+
<li>Name: Amrinder G, Krista F, Yoyo Y, Isaac W</li>
<li>Date: May 17, 2013</li>
<li>Date: May 17, 2013</li>
<li class="notebook_nested_start">Glycerol Stocked:</li>
<li class="notebook_nested_start">Glycerol Stocked:</li>

Latest revision as of 03:49, 22 June 2013

Ligations

  • Name: Yoyo Y
  • Date: May 1, 2013
  • Ligation of Parts – Upstream, Ligated at sites S & P:
    • J23100
    • J23113
    • J23108 +
    • J23108 –
    • All promoters already attached to Destination Plasmid J61002
  • Downstream, Ligated at sites X & P
    • J23100

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Restriction Digest

  • Name: Mackenzie C
  • Date: May 4, 2013
  • 35µL DNA, 14µL MM, 0.5µL Spe1, 0.5µL Pst1
  • Master Mix
    Milliq 36µl
    BSA 45µl
    10x buffer 2 NEB 45µl

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1% Agarose Gel of Promoter Constructs

  • Name: Mackenzie C
  • Date: May 4, 2013
  • Lane # Contents Volume
    1 1KB LADDER 6µL
    2 J23100_J61002 25µL
    3 J23100_J61002 25µL
    4 J23100_J61002 25µL
    5 J23100_J61002 25µL
    6 J23108_J61002 25µL
    7 J23108_J61002 25µL
    8 J23108_J61002 25µL
    9 J23108_J61002 25µL
    10 J23113_J61002 25µL
    11 J23113_J61002 25µL
    12 J23113_J61002 25µL
    13 J23113_J61002 25µL
    14 J23114_J61002 25µL
    15 J23114_J61002 25µL
    16 J23114_J61002 25µL
    17 J23114_J61002 25µL

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Gel Extraction

  • Date: May 4, 2013
  • J23108_J61002
  • J23113_J61002
  • J23114_J61002
  • J23100_J61002
  • Eluted 50 µL

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Transformation

  • Name: Mackenzie C
  • Date: May 5, 2013
  • Tube # Part # Plasmid Volume of Competent Cells
    1 J23100+J06702 J61002 20µL
    2 J23108+J06702 J61002 20µL
    3 J23113+J06702 J61002 20µL
    4 J23108-J06702 J61002 20µL

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Restriction

  • Name: Chris I
  • Date: May 7, 2013
  • Cut with ‘X’ and ‘P’
  • J06702–RBS-mCherry-DT

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Gel Extraction

  • Name: Katie T, Elaine B
  • Date: May 7, 2013
  • J06702
  • Eluted at 30µL
  • Gel Extraction Done on May 7, 2013

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Gel Extracted Parts on Conformation Gel

  • 1µl of 1kb Ladder ng/0.5µg
  • 2µl DNA in all samples
  • Gel Extracted Parts on Conformation Gel Image
    Lane # Content
    1 Ladder
    2 J06702
    3 J23113–J61002 mc05/04/13mdy
    4 J23108–J61002 mc05/04/13
    5 J23100–J61002 mc05/04/13
    6 J23114–J61002 mc05/04/13
    7 Ladder
    8 J23100–J 61002 EK150413dmy
    9 J23108–J61002 EK150413
    10 J23113–J61002EK150413
    11 J23114 –J61002 EK150413

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Gel Extraction

  • Name: Carissa K
  • Date: May 8, 2013
  • 2µL of J06702 mix with 4µL of each; J23100, J23108, J23113, J23114 all in plasmid J61002 (amp)
  • In the Thermo-cycler at 16°C overnight followed by heat kill.

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PCR of Ligation Mixture(PCR to verify insert in clone vector)

  • Name: Chris I
  • Date: May 9, 2013
  • X7 Master Mix, Taq polymerase
  • J23100_J61002 (control)
  • J06702_pSB1AK2 (control)
  • J23100_J61002_J06702
  • J23108_J601002_J06702
  • J23113_J61002_J06702
  • J23114_J61002_J06702

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Restriction of PCR Ligations Gel Conformation

  • Name: Patrick O
  • Date: May 13, 2013
  • Restriction of May 9th PCR ligation at E and P and ran on 1.0% Gel (refreshed ETH Bromide)
  • Ladder lane 2
  • 2space
  • J06702_pSB1AK2 (control)
  • 2spaces
  • J23100_J61002 (control)
  • spaces
  • J23100_J61002_J06702
  • J23108_J601002_J06702
  • J23113_J61002_J06702
  • J23114_J61002_J06702
  • Ladder
  • Conclusion: Ligations were not successful
  • Restriction of PCR Ligations Gel Conformation Image

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Transformation of Ligations

  • Date: May 14, 2013
  • Transformed ligation of J06702 with various promoters in plasmid J61002 : J23100, J23108, J23113, J23114 From May 8, 2013.
  • Transformed 3µL ligation mix into 30µL of DH5α competent cells, used puc19 control. Heat shocked for 30 seconds at 42°C, added 200µL warm LB, incubated at 37°C for 1 hour. Plated 100µL on amp LB Agar plates. Incubated overnight at 37°C.

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Ligation Round 2 of May 14th Gel Extracted Parts

  • 11µL dh20
  • 2µL t4 DNA ligase buffer
  • 4µL DNA J06702
  • 2µL DNA J23100, J23108, J23113, J23114 in plasmid J61002
  • 1µL T4 DNA Ligase
  • Into the Thermo-cycler overnight at 16°C.

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Picking Cells

  • Name: Yoyo Y, Amrinder G, Patrick O, Orion S
  • Date: May 15, 2013
  • Put 50µL of Amp resistance into 50mL of Lb media
  • Flasks:
    • J23100_J61002
    • J23108_J61002
    • J23113_J61002
    • J23114_J61002
    • J06702_pSB1AK2
  • Inserted tips of E. coli into each flask

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Picking Cells

  • Name: Amrinder G, Orion S
  • Date: May 16, 2013
  • Put 5µL of Amp into 5mL of Lb media
  • Flasks:
    • J23100_J61002
    • J23108_J61002
    • J23113_J61002
    • J23114_J61002
    • J06702_pSB1AK2
  • Inserted tips of E. coli into each tube

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10 Fold Miniprep

  • Name: Isaac, Patrick
  • Date: May 16, 2013
  • Spun down 50ml of culture in falcon tubes
  • 5000xg twice for 2 mins to collect cells
  • Resupended in 1ml solution1 2ml solution 2 and 3, 5ml solution 3
  • Spun down at 6000xg for 6 minutes to pellet cell debris
  • Eluted into 4 miniprep spin columns twice to reach maximum binding efficiency
    • Combined eluted minipreps into one sample totalling 200µL
  • Mini prep of (50µL EB):
    • J23100_J61002
    • J23108_J61002
    • J23113_J61002
    • J23114_J61002
    • J06702_pSB1AK2
  • Mini-prepped with EZ-10 columns
  • Eluted 35µL
  • Purified DNA in Erin’s Box

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Agarose Gel

  • Name: Krista F, Yoyo Y
  • Date: May 17, 2013
  • Restriction of:
    • 4μL DNA
    • 1μL Enzyme
    • 2.5μL Buffer
    • 17.5μL Water
    • J23100_J06702 J61002
    • J23108_J06702 J61002
    • J23113_J06702 J61002
    • J23114_J06702 J61002
    • J06702_J61002
  • Ladder: 2μL Ladder, 0.5μL Dye
  • Conformation Gel on May 17, 2013
  • Conformation of all 5 of May 16, 2013 minipreps
  • Well #(from left) DNA Parts Concentration
    2 ladder 2μL Ladder/0.5μL Dye
    4 J23100_J06702 J61002 25μL DNA/5μL Dye
    6 J23108_J06702 J61002 25μL DNA/5μL Dye
    8 J23113_J06702 J61002 25μL DNA/5μL Dye
    10 J23114_J06702 J61002 25μL DNA/5μL Dye
    12 J06702 J61002 25μL DNA/5μL Dye
    14 ladder 2μL Ladder/0.5μL Dye

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Miniprep

  • Name: Amrinder G, Krista F
  • Date: May 17, 2013
  • Mini prep of (35µL EB):
    • J23100_J61002
    • J23108_J61002
    • J23113_J61002
    • J23114_J61002
    • Mini-prepped with EZ-10 columns
    • Eluted 35µL
    • Purified DNA in Erin’s Box
  • Inserted tips of E. coli into each flask

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Glycerol Stock

  • Name: Amrinder G, Krista F, Yoyo Y, Isaac W
  • Date: May 17, 2013
  • Glycerol Stocked:
    • J23100_J61002
    • J23108_J61002
    • J23113_J61002
    • J23114_J61002

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Retrieved from "http://2013hs.igem.org/Team:Lethbridge_Canada/notebook_may"