Team:TU Darmstadt/Protocols/SamplePreparationEDX
From 2012.igem.org
(Created page with "'''Preparation of Escherichia Coli for the energy dispersive X-ray spectroscopy (EDX)''' NOTE: The pellet must be about 0.25 g and the preparation takes about 4 days '''Prima...") |
|||
Line 1: | Line 1: | ||
- | + | <html> | |
+ | <link rel="stylesheet" href="https://2012.igem.org/wiki/index.php?title=Team:TU_Darmstadt/css&action=raw&ctype=text/css" type="text/css" /> | ||
+ | <div id="TUD"> | ||
+ | <div id="top"> | ||
+ | <ul> | ||
+ | <li><a href="http://www.igem.tu-darmstadt.de/igem/projekt/index.en.jsp" title="iGEM">iGEM@TUD</a></li> | ||
+ | <li><a href="/Team:TU_Darmstadt" title="Home">Home</a></li> | ||
+ | <li><a href="/Team:TU_Darmstadt/Project" title="Project">Project</a><ul> | ||
+ | <li><a href="/Team:TU_Darmstadt/Project" title="Team:Overview">Overview</a></li> | ||
+ | <li><a href="/Team:TU_Darmstadt/Project/Degradation" title="Degradation">1. Degradation</a></li> | ||
+ | <li><a href="/Team:TU_Darmstadt/Project/Transport" title="Transport">2. Transport</a></li> | ||
+ | <li><a href="/Team:TU_Darmstadt/Project/Metabolism" title="Metabolism">3. Metabolism</a></li> | ||
+ | <li><a href="/Team:TU_Darmstadt/Project/Material_Science" title="Material Science">4. Material Science</a></li> | ||
+ | <li><a href="/Team:TU_Darmstadt/Project/Simulation" title="Simulation">5. Simulation</a></li> | ||
+ | <li><a href="/Team:TU_Darmstadt/Project/Ecology" title="Ecology">Ecology</a></li> | ||
+ | <li><a href="/Team:TU_Darmstadt/Project/Philosophy" title="Philosophy">Philosophy</a></li></ul></li> | ||
+ | <li><a href="/Team:TU_Darmstadt/Team" title="Team:TU_Darmstadt/Team">Team</a><ul> | ||
+ | <li><a href="/Team:TU_Darmstadt/Team" title="Team:TU_Darmstadt/Team">Members</a></li> | ||
+ | <li><a href="/Team:TU_Darmstadt/Supporters" title="Team:TU_Darmstadt/Supporters">Supporters</a></li></ul></li> | ||
+ | <li><a href="/Team:TU_Darmstadt/Parts" title="BioBricks">BioBricks</a></li> | ||
+ | <li><a href="/Team:TU_Darmstadt/Documentation" title="Documentation">Documentation</a><ul> | ||
+ | <li><a href="/Team:TU_Darmstadt/Documentation" title="Documentation">Overview</a></li> | ||
+ | <li><a href="/Team:TU_Darmstadt/Labjournal" title="Labjournal">Labjournal</a></li> | ||
+ | <li><a href="/Team:TU_Darmstadt/Protocols" title="Protocols">Protocols</a></li> | ||
+ | <li><a href="/Team:TU_Darmstadt/Materials" title="Materials">Materials</a></li> | ||
+ | <li><a href="/Team:TU_Darmstadt/Modeling" title="Modeling">Modeling</a></li> | ||
+ | <li><a href="/Team:TU_Darmstadt/Safety" title="Safety">Safety</a></li> | ||
+ | <li><a href="/Team:TU_Darmstadt/Downloads" title="Downloads">Downloads</a></li></ul></li> | ||
+ | <li><a href="/Team:TU_Darmstadt/Human_Practice" title="Human Practice">Human Practice</a><ul> | ||
+ | <li><a href="/Team:TU_Darmstadt/Human_Practice/Panel_Discussion " title="Panel Discussion">Panel Discussion</a></li> | ||
+ | <li><a href="/Team:TU_Darmstadt/Human_Practice/Symposia" title="Symposia">Symposia</a></li> | ||
+ | <li><a href="/Team:TU_Darmstadt/Human_Practice/Classes" title="Classes">Classes</a></li></ul></li> | ||
+ | <li><a href="/Team:TU_Darmstadt/Sponsors" title="Sponsors">Sponsors</a><ul> | ||
+ | <li><a href="/Team:TU_Darmstadt/Sponsors" title="Sponsors">Overview</a></li> | ||
+ | <li><a href="/Team:TU_Darmstadt/Contact" title="Contact">Benefits</a></li></ul></li> | ||
+ | </ul> | ||
+ | <div id="igem"><a href="https://2012.igem.org/Main_Page"></a></div> | ||
+ | </div> | ||
+ | <!-- end #menu --> | ||
+ | </html> | ||
+ | |||
+ | <span style="font-size:200%;"><span style="color:#00689D;">Preparation of Escherichia Coli for the energy dispersive X-ray spectroscopy (EDX)</span></span> | ||
+ | |||
+ | ==Fixation== | ||
Line 32: | Line 75: | ||
- | + | ==Dehydration== | |
Line 39: | Line 82: | ||
- | + | ==Infiltration== | |
Line 49: | Line 92: | ||
- | + | ==Polymerisation== | |
Line 57: | Line 100: | ||
- | + | ==Cutting== | |
Line 64: | Line 107: | ||
- | + | ==Mixtures== | |
'''Pre-fixationmedia''' | '''Pre-fixationmedia''' |
Revision as of 06:58, 26 September 2012
Preparation of Escherichia Coli for the energy dispersive X-ray spectroscopy (EDX)
Contents |
Fixation
NOTE: The pellet must be about 0.25 g and the preparation takes about 4 days
Primary Fixation-step
- give about 1 ml pre-fixationmixure to your pellet and incubate at room temperature for at least 1 hour
NOTE: you have to centrifuged your pellet after each step (about 30-45 sec at max. rpm)
Washing-step
- wash your pellet 4 times with about 750µL 0.1 M Cacodylate-buffer (CaCo) pH 7.4 for at least 15 min at RT
Secondary fixation-step
- give about 750µL 0.5 % Osmium in 0.1 M CaCo Puffer pH 7.4 to your pelett and incubate at RT at least 1 hour
washing-step
- wash your pellet 2 times with about 750µL 0.1 M CaCo buffer pH 7.4 for at least 10 min and 2 times with bidest H20 for 10 min
Dehydration
- give to your pellett about 750µL 30%,50%,90%,100% acetone and incubate each pellet at RT for at least 10 min
- give to your pelett about 750µL 100% acetone (dried) and incubate 2 times at RT for at least15 min
Infiltration
- give to your pelett about 500µL 25 % SPURR (in acetone) and incubate at RT for at least 45 min
- give to your pelett about 500µL 50 % SPURR (in acetone) and incubate at RT for at least 45 min
- give to your pelett about 500µL 75 % SPURR (in acetone) and incubate at RT for at least 45 min
- give to your pelett 2 times about 500µL 100 % SPURR (in acetone) and incubate at RT for at least
- give to your pelett about 500µL 100 % SPURR (in acetone) and incubate at 4 °C overnight.
Polymerisation
NOTE: your pellet have to be on the bottom of the capsule
- give to your pelett fresh mixed SPURR and fill a part of your pellet into a capsule and incubate at 74°C over night.
Cutting
- cut your polymererised capsule with a.... in a thicker than 100 nm rectangles
- your sample ist ready for EDX
Mixtures
Pre-fixationmedia
1. 0.1 M Cocadynaltebuffer pH 7.4 (with acentic acid)
(C2H6AsO2Na x 3 H2O Dimethyle arsine acid sodium salt, 214. 13 g/mol)
for 50 mL 2.14 g Dimethyle arsine acid sodium salt
2. 25% Glutaralaldehyde solution
3. 10 % Formalaldehyde solution
freshly mixed: annul 0.5 g Paraformaldehyde in 5 mL ddH2O and heat up to 60 °C. Add dropwise NaOH until a clear solution occurs.
4. ddH2O
Amount for 10 mL pre-fixationmedia
1. 5 mL (endconcentration 0.1 M)
2. 1 mL (endconcentration 2.5 %)
3. 2 mL (endconcentration 2 %)
4. 2 mL
E.R.L-embedding media
1. 3,4 epoxycyclohexyl methyl carboxylate 2.5 g
2. D.E.R. 736 epoxy resin 1.0 g
3. Nonenyl-succinic acid 6.5 g
4. Dimetyl-aminomethanol 0.1 g