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Team:Newcastle/Scanning EM
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| - | This is a standard method for Scanning Electron Microscopy. Specimens vary greatly and the final protocol should be decided by referring to text books and publications. | + | This is a standard method for preparing samples for Scanning Electron Microscopy. Specimens vary greatly and the final protocol should be decided by referring to text books and publications. |
==Fixation== | ==Fixation== | ||
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==Gold coating== | ==Gold coating== | ||
| - | Coat with | + | Coat with 15 nm of gold using a Polaron SEM Coating Unit. |
{{Team:Newcastle/footer}} | {{Team:Newcastle/footer}} | ||
Revision as of 22:06, 27 October 2010
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Contents |
Scanning EM
This is a standard method for preparing samples for Scanning Electron Microscopy. Specimens vary greatly and the final protocol should be decided by referring to text books and publications.
Fixation
Fix in 2% Gluteraldehyde in Sorensons Phosphate Buffer overnight (minimum).
Rinse in Sorensons Phosphate Buffer 2x 15 mins.
Dehydration
- 25% ethanol: 30 mins.
- 50% ethanol: 30 mins.
- 75% ethanol: 30 mins.
- 100% ethanol: 1 hr.
- 100% ethanol: 1 hr.
Once in 100% ethanol, samples are dried using a Baltec Critical Point Dryer.
Mounting
Mount on an aluminium stub with Achesons Silver ElectroDag.
Gold coating
Coat with 15 nm of gold using a Polaron SEM Coating Unit.
   
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