Team:Aachen/Notebook/Protocols

From 2014.igem.org

(Difference between revisions)
m (→Gels)
m (→Protocols)
 
(186 intermediate revisions not shown)
Line 1: Line 1:
 +
__NOTOC__
 +
{{CSS/Main}}
 +
{{Team:Aachen/Stylesheet}}
{{Team:Aachen/Header}}
{{Team:Aachen/Header}}
 +
<span id="partners"></span>
-
__TOC__
+
=Protocols=
-
= Media =
+
In our experiments, we often re-used protocols for basic experimental steps. For a better overview, we split our protocols into four categories:
-
== LB medium ==
+
-
# weight components
+
-
::* '''5 g/L NaCl'''
+
-
::* '''10 g/L tryptone'''
+
-
::* '''5 g/L yeast extract'''
+
-
::* (15 g/L agar for plates)
+
-
# fill up to 1&nbsp;L with deionized water
+
-
# '''mix well''' by shaking
+
-
# autoclave
+
-
## autoclaving tape, caps slightly unscrewed
+
-
## base of the pot has to be covered with deionized water
+
-
## close lid
+
-
## heat '''level 3 until the pressure valve opens'''
+
-
## reduce '''heat level to 1.5'''
+
-
## set timer to '''20 minutes'''
+
-
## turn heater off
+
-
## '''wait until the pressure valve retracts''' (30-45 minutes)
+
-
## open, close caps & shake
+
-
# for plates, wait until you can touch the bottle ('''<60 °C''', clean bench!)
+
-
# add antibiotics and '''shake''' (gloves!)
+
-
== Hartmans minimal medium (HM) ==
+
* 2D Detection of IPTG & HSL
 +
* Culture Media
 +
* Molecular Biological Methods
 +
* Analytical Methods
 +
To access the protocols, please click on the respective category panel below:
 +
<center>
 +
<html><ul class="team-grid" style="width:1064px;">
-
= Agar Chips =
+
<li style="width:220px;margin-left: 23px;margin-right: 23px;margin-bottom: 23px;margin-top: 23px;">
-
 
+
<a href="https://2014.igem.org/Team:Aachen/Notebook/Protocols/detection" style="color:black;">
-
= Transformation =
+
    <div class="team-item team-info" style="width:214px;height:214px;" >
-
== Heat Shock ==
+
      <div class="menukachel" style="top: 32%;line-height: 1.5em;">2D Detection of<br/>IPTG & HSL</div>
-
# thaw cells on ice
+
      <!-- <br/><br/>
-
# add 1&nbsp;µl of plasmid DNA
+
      <b>Principle of Operation</br>
-
# incubate on ice for 30'
+
      <br/><br/>
-
# heat shock at 42&nbsp;°C for 60''
+
      click for more information -->
-
# incubate on ice for 5'
+
    </div>
-
# add 200&nbsp;µl of SOC media
+
    <div class="team-item team-img" style="background: url(https://static.igem.org/mediawiki/2014/2/22/Aachen_14-10-14_button_chip_manufacturing_ipo.png); norepeat scroll 0% 0% transparent; background-size:100%;width:214px;height:214px;"> </div></a>
-
# incubate at 37&nbsp;°C for 2&nbsp;h
+
  </li>
-
# plate 20&nbsp; and 200&nbsp;µl on plates with the appropiate antibiotic
+
-
 
+
-
== Electroporation ==
+
-
 
+
-
= PCR =
+
-
== Colony PCR ==
+
-
 
+
-
== QuikChange ==
+
-
 
+
-
= Clonings =
+
-
== Restriction Digest ==
+
-
 
+
-
== Ligation ==
+
-
 
+
-
== Gibson Assembly ==
+
-
 
+
-
 
+
-
 
+
-
 
+
-
= SDS-PAGE =
+
-
For some SDS-PAGEs we used BioRad ready made gels.
+
-
 
+
-
The recipe of the self-made SDS is as follows:
+
-
 
+
-
=== 3.5x Buffer ===
+
-
 
+
-
 
+
-
=== Gels ===
+
-
{| class="wikitable" style="text-align: right;"
+
-
!
+
-
!! style="border-left: 2px solid #404040;" colspan="3"|1mm 12 % RUNNING Gel
+
-
!! style="border-left: 2px solid #404040;" colspan="3"|1mm 8 % RUNNING Gel
+
-
!! style="border-left: 2px solid #404040; background-color:#8ebae5;" colspan="3"|1mm 4 % STACKING Gel
+
-
|-
+
-
|
+
-
| style="border-left: 2px solid #404040;"| '''1x''' || '''2x''' || '''4x'''
+
-
| style="border-left: 2px solid #404040;"| '''1x''' || '''2x''' || '''4x'''
+
-
| style="border-left: 2px solid #404040;"| '''1x''' || '''2x''' || '''4x'''
+
-
|-
+
-
| '''H{{sub|2}}O'''
+
-
| style="border-left: 2px solid #404040;"| 1.669 ml || 3.337 ml || 6.674 ml
+
-
| style="border-left: 2px solid #404040;"| 2.45 ml || 4.9 ml || 9.8 ml
+
-
| style="border-left: 2px solid #404040;"| 1.421 ml || 2.842 ml || 5.684 ml
+
-
|-
+
-
| '''3.5x Gel Buffer'''
+
-
| style="border-left: 2px solid #404040;"| 1.613 ml || 3.225 ml || 6.45 ml
+
-
| style="border-left: 2px solid #404040;"| 1.613 ml || 3.225 ml || 6.45 ml
+
-
| style="border-left: 2px solid #404040;"| 0.7 ml || 1.4 ml || 2.8 ml
+
-
|-
+
-
| '''30 % Acrylamide (37.5:1)'''
+
-
| style="border-left: 2px solid #404040;"| 2.344 ml || 4.687 ml || 9.374 ml
+
-
| style="border-left: 2px solid #404040;"| 1.563 ml || 3.125 ml || 6.25 ml
+
-
| style="border-left: 2px solid #404040;"| 0.329 ml || 0.658 ml || 1.316 ml
+
-
|-
+
-
| '''10 % APS'''
+
-
| style="border-left: 2px solid #404040;"| 22.5 µl || 45 µl || 90 µl
+
-
| style="border-left: 2px solid #404040;"| 22.5 µl || 45 µl || 90 µl
+
-
| style="border-left: 2px solid #404040;"| 10.5 µl || 21 µl || 42 µl
+
-
|-
+
-
| '''TEMED'''
+
-
| style="border-left: 2px solid #404040;"| 2.25 µl || 4.5 µl || 9 µl
+
-
| style="border-left: 2px solid #404040;"| 2.25 µl || 4.5 µl || 9 µl
+
-
| style="border-left: 2px solid #404040;"| 4.9 µl || 9.8 µl || 19.6 µl
+
-
|-
+
-
|}
+
 +
<li style="width:220px;margin-left: 23px;margin-right: 23px;margin-bottom: 23px;margin-top: 23px;">
 +
<a href="https://2014.igem.org/Team:Aachen/Notebook/Protocols/Culture_medium_and_conditions" style="color:black;">
 +
    <div class="team-item team-info" style="width:214px;height:214px;" >
 +
      <div class="menukachel" style="top: 40%;line-height: 1.5em;">Culture Media</div>
 +
      <!-- <br/><br/>
 +
      <b>Principle of Operation</br>
 +
      <br/><br/>
 +
      click for more information -->
 +
    </div>
 +
<div class="team-item team-img" style="background: url(https://static.igem.org/mediawiki/2014/1/10/Aachen_14-10-13_Yellow_Flask_iNB.png); norepeat scroll 0% 0% transparent; background-size:100%;width:214px;height:214px;"> </div></a>
 +
  </li>
 +
<li style="width:220px;margin-left: 23px;margin-right: 23px;margin-bottom: 23px;margin-top: 23px;">
 +
<a href="https://2014.igem.org/Team:Aachen/Notebook/Protocols/Molecular_biological_methods" style="color:black;">
 +
    <div class="team-item team-info" style="width:214px;height:214px;">
 +
      <div class="menukachel" style="top: 25%;line-height: 1.5em;">Molecular Biological Methods</div>
 +
      <!-- <br/><br/>
 +
      <b>Principle of Operation</br>
 +
      <br/><br/>
 +
      click for more information -->       
 +
    </div>
 +
    <div class="team-item team-img" style="background: url(https://static.igem.org/mediawiki/2014/7/75/Aachen_14-10-14_Eppi_with_green_cells_panel_iNB.png); norepeat scroll 0% 0% transparent; background-size:100%;width:214px;height:214px;"> </div></a>
 +
  </li>
 +
<li style="width:220px;margin-left: 23px;margin-right: 23px;margin-bottom: 23px;margin-top: 23px;">
 +
<a href="https://2014.igem.org/Team:Aachen/Notebook/Protocols/Analytical_methods" style="color:black;">
 +
    <div class="team-item team-info" style="width:214px;height:214px;" >
 +
      <div class="menukachel" style="top: 32%;line-height: 1.5em;">Analytical Methods</div>
 +
      <!-- <br/><br/>
 +
      <b>Principle of Operation</br>
 +
      <br/><br/>
 +
      click for more information -->
 +
    </div>
 +
    <div class="team-item team-img" style="background: url(https://static.igem.org/mediawiki/2014/4/4d/Aachen_14-10-14_Lense_panel_iNB.png); norepeat scroll 0% 0% transparent; background-size:100%;width:214px;height:214px;"> </div></a>
 +
  </li>
 +
</ul></html>
 +
</center>
{{Team:Aachen/Footer}}
{{Team:Aachen/Footer}}

Latest revision as of 00:49, 18 October 2014

Protocols

In our experiments, we often re-used protocols for basic experimental steps. For a better overview, we split our protocols into four categories:

  • 2D Detection of IPTG & HSL
  • Culture Media
  • Molecular Biological Methods
  • Analytical Methods

To access the protocols, please click on the respective category panel below:

Contact Disclaimer

Retrieved from "http://2014.igem.org/Team:Aachen/Notebook/Protocols"