DNA extraction - Salting Out: Difference between revisions

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==Curators==
==Curators==
Marcus McHale [[Special:Emailuser/Marcus McHale|Email me through OpenWetWare]]
*Marcus McHale [[Special:Emailuser/Marcus McHale|Email me through OpenWetWare]]


*This protocol has evolved with me and I am sure many others, please share your optimisations.
''Anyone should feel free to add themselves as a curator for this consensus protocol.  You do not need to be a curator in order to contribute.  The OpenWetWare community is currently [[OpenWetWare:Information management/Protocol curators|discussing the idea of protocol curators]].  Please contribute.''
''Anyone should feel free to add themselves as a curator for this consensus protocol.  You do not need to be a curator in order to contribute.  The OpenWetWare community is currently [[OpenWetWare:Information management/Protocol curators|discussing the idea of protocol curators]].  Please contribute.''


==Abstract==
==Abstract==
Simple procedure for DNA extraction using salt
*Simple procedure for DNA extraction using salt


==Materials==
==Materials==
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==Critical steps==
==Critical steps==
#After adding sodium acetate and centrifuging be careful not to transfer any of the white solid (SDS) into the fresh tube
*After adding sodium acetate and centrifuging be careful not to transfer any of the white solid (SDS) into the fresh tube
#Ensure to dry the pelletted DNA completely before attempting to resuspend
*Ensure to dry the pelletted DNA completely before attempting to resuspend


==Troubleshooting==
==Troubleshooting==


==Notes==
==Notes==
#This protocol has evolved with me and I am sure many others, please share your optimisations.
*You may wish to kill the Proteinase K (95°C, 10 minutes) after the extraction though if you are proceding straight to PCR (and don't leave your reactions sitting around before thermal cycling) the denaturation step will take care of that
#You may wish to kill the Proteinase K (95°C, 10 minutes) after the extraction though if you are proceding straight to PCR (and don't leave your reactions sitting around before thermal cycling) the denaturation step will take care of that


==Acknowledgments==
==Acknowledgments==
#Damien Broderick from Queensland Depaqrtment of Primary Industries and Fisheries supplied me with his version of this protocol to start me off.
*Damien Broderick from Queensland Depaqrtment of Primary Industries and Fisheries supplied me with his version of this protocol to start me off.


==References==
==References==
Miller SA, Dykes DD, Polesky HF (1988) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Research, 16, 1215–1215.
*Miller SA, Dykes DD, Polesky HF (1988) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Research, 16, 1215–1215.


==Specific Protocols==
==Specific Protocols==
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