Difference between revisions of "Team:Bielefeld-CeBiTec/Media"
Line 74: | Line 74: | ||
</div> | </div> | ||
<div id="collapseThree" class="panel-collapse collapse"> | <div id="collapseThree" class="panel-collapse collapse"> | ||
+ | <div class="panel-body"> | ||
+ | <ul> | ||
+ | <li>For each litre of solution: </li> | ||
+ | <ul> | ||
+ | <li>242 g Tris Base (MW=121.1) </li> | ||
+ | <li>57.1 ml Glacial Acetic Acid </li> | ||
+ | <li>100 ml 0.5 M EDTA </li> | ||
+ | </ul> <br> | ||
+ | <li>mix Tris with stir bar to dissolve in about 600 ml of ddH<sub>2</sub>O. </li> | ||
+ | <li>add the EDTA and Acetic Acid. </li> | ||
+ | <li>bring final volume to 1 l with ddH20. </li> | ||
+ | <li>store at room temperature. </li> <br> | ||
+ | <li>Note: Final (1x) working concentration: </li> | ||
+ | <ul> | ||
+ | <li>0.04 M Tris - Acetate </li> | ||
+ | <li>0.001 M EDTA </li> | ||
+ | </ul> | ||
+ | </ul> | ||
+ | </div> | ||
+ | </div> | ||
+ | </div> | ||
+ | <div class="panel panel-default"> | ||
+ | <div class="panel-heading"> | ||
+ | <h4 class="panel-title"> | ||
+ | <a data-toggle="collapse" href="#collapseFour">Lysis and binding buffer for purification of lacI</a> | ||
+ | </h4> | ||
+ | </div> | ||
+ | <div id="collapseFour" class="panel-collapse collapse"> | ||
+ | <div class="panel-body"> | ||
+ | <ul> | ||
+ | <li>For each 200 ml of solution: </li> | ||
+ | <ul> | ||
+ | <li>5.844 g NaCl </li> | ||
+ | <li>0.272 g imidazole </li> | ||
+ | <li>5.8 ml of 86 % glycerol </li> | ||
+ | <li>0.406 g MgCl<sub>2</sub></li> | ||
+ | <li>0.2 g lysozyme</li> | ||
+ | </ul> <br> | ||
+ | <li>Add all these ingredients to a 50 mM sodium phosphate buffer (pH 8.0). Prior to use add DTT to a final concentration of 1mM. </li> | ||
+ | |||
+ | <li>store at room temperature. </li> <br> | ||
+ | <li>Note: Final (1x) working concentration: </li> | ||
+ | <ul> | ||
+ | <li>0.04 M Tris - Acetate </li> | ||
+ | <li>0.001 M EDTA </li> | ||
+ | </ul> | ||
+ | </ul> | ||
+ | </div> | ||
+ | </div> | ||
+ | </div> | ||
+ | <div class="panel panel-default"> | ||
+ | <div class="panel-heading"> | ||
+ | <h4 class="panel-title"> | ||
+ | <a data-toggle="collapse" href="#collapseFive">50X TAE Stock Solution</a> | ||
+ | </h4> | ||
+ | </div> | ||
+ | <div id="collapseFive" class="panel-collapse collapse"> | ||
+ | <div class="panel-body"> | ||
+ | <ul> | ||
+ | <li>For each litre of solution: </li> | ||
+ | <ul> | ||
+ | <li>242 g Tris Base (MW=121.1) </li> | ||
+ | <li>57.1 ml Glacial Acetic Acid </li> | ||
+ | <li>100 ml 0.5 M EDTA </li> | ||
+ | </ul> <br> | ||
+ | <li>mix Tris with stir bar to dissolve in about 600 ml of ddH<sub>2</sub>O. </li> | ||
+ | <li>add the EDTA and Acetic Acid. </li> | ||
+ | <li>bring final volume to 1 l with ddH20. </li> | ||
+ | <li>store at room temperature. </li> <br> | ||
+ | <li>Note: Final (1x) working concentration: </li> | ||
+ | <ul> | ||
+ | <li>0.04 M Tris - Acetate </li> | ||
+ | <li>0.001 M EDTA </li> | ||
+ | </ul> | ||
+ | </ul> | ||
+ | </div> | ||
+ | </div> | ||
+ | </div> | ||
+ | <div class="panel panel-default"> | ||
+ | <div class="panel-heading"> | ||
+ | <h4 class="panel-title"> | ||
+ | <a data-toggle="collapse" href="#collapseSix">50X TAE Stock Solution</a> | ||
+ | </h4> | ||
+ | </div> | ||
+ | <div id="collapseSix" class="panel-collapse collapse"> | ||
<div class="panel-body"> | <div class="panel-body"> | ||
<ul> | <ul> |
Revision as of 19:58, 6 July 2015
Media
- For 1 liter LB:
- 20 g LB powder
- Fill the bottle with deionized H2O
- For 1 liter LB-plates:
- 18 g LB powder
- 16 g Select Agar
- Fill the bottle with deionized H2O
- Add the following components for 900 ml of distilled H2O:
- 20 g Trypton
- 5 g Bacto Yeast Extract
- 2 ml of 5 M NaCl
- 2.5 ml of 1 M KCl
- 10 ml of 1 M MgCl2
- 10 ml of 1 M MgSO4
- 20 ml of 1 M glucose
Buffers
- For each litre of solution:
- 242 g Tris Base (MW=121.1)
- 57.1 ml Glacial Acetic Acid
- 100 ml 0.5 M EDTA
- mix Tris with stir bar to dissolve in about 600 ml of ddH2O.
- add the EDTA and Acetic Acid.
- bring final volume to 1 l with ddH20.
- store at room temperature.
- Note: Final (1x) working concentration:
- 0.04 M Tris - Acetate
- 0.001 M EDTA
- For each 200 ml of solution:
- 5.844 g NaCl
- 0.272 g imidazole
- 5.8 ml of 86 % glycerol
- 0.406 g MgCl2
- 0.2 g lysozyme
- Add all these ingredients to a 50 mM sodium phosphate buffer (pH 8.0). Prior to use add DTT to a final concentration of 1mM.
- store at room temperature.
- Note: Final (1x) working concentration:
- 0.04 M Tris - Acetate
- 0.001 M EDTA
- For each litre of solution:
- 242 g Tris Base (MW=121.1)
- 57.1 ml Glacial Acetic Acid
- 100 ml 0.5 M EDTA
- mix Tris with stir bar to dissolve in about 600 ml of ddH2O.
- add the EDTA and Acetic Acid.
- bring final volume to 1 l with ddH20.
- store at room temperature.
- Note: Final (1x) working concentration:
- 0.04 M Tris - Acetate
- 0.001 M EDTA
- For each litre of solution:
- 242 g Tris Base (MW=121.1)
- 57.1 ml Glacial Acetic Acid
- 100 ml 0.5 M EDTA
- mix Tris with stir bar to dissolve in about 600 ml of ddH2O.
- add the EDTA and Acetic Acid.
- bring final volume to 1 l with ddH20.
- store at room temperature.
- Note: Final (1x) working concentration:
- 0.04 M Tris - Acetate
- 0.001 M EDTA