Team:Alberta/Notebook/protocols/gel extraction
From 2010.igem.org
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- | {{Team:Alberta/navbar| | + | {{Team:Alberta/navbar|notebook=selected}} |
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+ | {{Team:Alberta/beginLeftSideBar|toc=NO}} | ||
+ | |||
+ | |||
+ | ==General Protocols== | ||
+ | ----------------------------- | ||
+ | *[[Team:Alberta/Notebook/protocols/invitro_biobyte_assembly | In Vitro BioByte Assembly]] | ||
+ | ----------------------------- | ||
+ | *[[Team:Alberta/Notebook/protocols/LB | LB Plates and Broth]] | ||
+ | |||
+ | *[[Team:Alberta/Notebook/protocols/transformations |Transformations]] | ||
+ | |||
+ | *[[Team:Alberta/Notebook/protocols/overnight |5mL Overnight ]] | ||
+ | |||
+ | *[[Team:Alberta/Notebook/protocols/glycerol | Glycerol Stock ]] | ||
+ | ----------------------------- | ||
+ | *[[Team:Alberta/Notebook/protocols/miniprep | Plasmid Miniprep ]] | ||
+ | |||
+ | *[[Team:Alberta/Notebook/protocols/digest | Restriction Digest ]] | ||
+ | |||
+ | *[[Team:Alberta/Notebook/protocols/vector_dephos | Vector Dephosphorylation]] | ||
+ | |||
+ | *[[Team:Alberta/Notebook/protocols/ligation | Ligation ]] | ||
+ | ----------------------------- | ||
+ | *[[Team:Alberta/Notebook/protocols/agarose_gel | Agarose Gel Electrophoresis ]] | ||
+ | |||
+ | *[[Team:Alberta/Notebook/protocols/gel_extraction | Gel Extraction ]] | ||
+ | ----------------------------- | ||
+ | *[[Team:Alberta/Notebook/protocols/pcr | PCR]] | ||
+ | |||
+ | *[[Team:Alberta/Notebook/protocols/colony_pcr | Colony PCR ]] | ||
+ | |||
+ | *[[Team:Alberta/Notebook/protocols/pcr_purification | PCR Purification ]] | ||
+ | ----------------------------- | ||
+ | *[[Team:Alberta/Notebook/protocols/labelling | Sample Labelling Conventions]] | ||
+ | |||
+ | *[[Team:Alberta/Notebook/protocols/sequencing | Fluorescent Sequencing Reaction]] | ||
+ | |||
+ | *[[Team:Alberta/Notebook/protocols/primer_design | Primer Design]] | ||
+ | ----------------------------- | ||
+ | |||
+ | |||
+ | {{Team:Alberta/endMainContent}} | ||
+ | |||
- | |||
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Latest revision as of 02:29, 27 October 2010
Gel Extraction
Reagents:
- Clean scalpel
- Transilluminator
- Eppendorf tube
- Gel extraction kit
- 55oC water bath
- Vortex
- Microfuge
Procedure:
- Place the gel on the transilluminator. Put on face shield and gloves.
- Turn on transilluminator and quickly make four slices; one on each side of the band you want to cut out and turn transilluminator off. Keep exposure to a minimum.
- Pry out the gel ‘cube’ and place it in an eppendorf tube.
- Follow instructions on pp. 25 of [http://www.qiagen.com/literature/render.aspx?id=103715 QIAQuick Spin Handbook].