Team:HKUST/Protocols/gel cut
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(New page: 6. Cutting bands on the gel Purpose: To extract specific DNA fragment. Procedure: a.Visualize the bands under UV light. Use long-wavelength UV to minimize damage to the DNA. b...) |
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- | b.Cut the band with a clean razor blade. | + | <title>Salt and Soap template</title> |
- | c.Turn the gel slice on its side to trim off extra agarose. Place the gel in a microcentrifuge tube. | + | </head> |
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+ | <div class="contentlist"> <h3>a</h3> | ||
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+ | <p>Cutting bands on the gel</p> | ||
+ | |||
+ | <p> Purpose: To extract specific DNA fragment.</p> | ||
+ | |||
+ | <p>Procedure: </p> | ||
+ | a.Visualize the bands under UV light. Use long-wavelength UV to minimize damage to the DNA. <br> | ||
+ | b.Cut the band with a clean razor blade.<br> | ||
+ | c.Turn the gel slice on its side to trim off extra agarose. Place the gel in a microcentrifuge tube.</p> | ||
+ | <p> Tips: </p> | ||
+ | EB staining is needed for higher resolution under UV light. | ||
+ | <br><br> | ||
+ | <p> Safety tips: </p> | ||
+ | 1. ermission is needed from technician before doing this! Follow the safety instruction in the room.<br><br> | ||
+ | 2.When using UV light, protect your skin by wearing safety goggles or a face shield, gloves, and a lab coat. <br><br> | ||
+ | <ul> | ||
+ | <li><a href="https://2009.igem.org/Team:HKUST/Protocols/Agarose_gel" >Agarose gel preparation and gel | ||
+ | electrophoresis</a></li> | ||
+ | <li><a href="https://2009.igem.org/Team:HKUST/Protocols/PCR">PCR (Taq, Vent)</a></li> | ||
+ | <li><a href="https://2009.igem.org/Team:HKUST/Protocols/PCR_cleanup">PCR product clean-up</a></li> | ||
+ | <li><a href="https://2009.igem.org/Team:HKUST/Protocols/Enzyme_digestion"> Enzyme digestion (vector, insert)</a></li> | ||
+ | <li><a href="https://2009.igem.org/Team:HKUST/Protocols/plasmid_extraction"> Plasmid DNA extraction</a></li> | ||
+ | <li><a href="https://2009.igem.org/Team:HKUST/Protocols/gel_cut"> Gel cutting</a></li> | ||
+ | <li><a href="https://2009.igem.org/Team:HKUST/Protocols/gel_extraction"> Gel extraction</a></li> | ||
+ | <li><a href="https://2009.igem.org/Team:HKUST/Protocols/Ethanol_precipitation"> Ethanol precipitation</a></li> | ||
+ | <li><a href="https://2009.igem.org/Team:HKUST/Protocols/Ligation"> Ligation</a></li> | ||
+ | <li><a href="https://2009.igem.org/Team:HKUST/Protocols/Transformation_to_Ecoli"> Transformation to E.coli</a></li> | ||
+ | <li><a href="https://2009.igem.org/Team:HKUST/Protocols/Transformation_to_yeast">Transformation to | ||
+ | yeast</a></li> | ||
+ | <li><a href="https://2009.igem.org/Team:HKUST/Protocols/Cell_lysis"> Cell lysis</a></li> | ||
+ | <li><a href="https://2009.igem.org/Team:HKUST/Protocols/Yeast_genomic_DNA_extraction"> Yeast genomic DNA | ||
+ | extraction</a></li> | ||
+ | <li><a href="https://2009.igem.org/Team:HKUST/Protocols/Western_blotting"> Western blotting</a></li> | ||
+ | <li><a href="https://2009.igem.org/Team:HKUST/Protocols/GFP_testing"> GFP testing</a></li> | ||
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Latest revision as of 09:55, 20 October 2009
a
Cutting bands on the gel
Purpose: To extract specific DNA fragment.
Procedure:
a.Visualize the bands under UV light. Use long-wavelength UV to minimize damage to the DNA.b.Cut the band with a clean razor blade.
c.Turn the gel slice on its side to trim off extra agarose. Place the gel in a microcentrifuge tube.
Tips:
EB staining is needed for higher resolution under UV light.Safety tips:
1. ermission is needed from technician before doing this! Follow the safety instruction in the room.2.When using UV light, protect your skin by wearing safety goggles or a face shield, gloves, and a lab coat.
- Agarose gel preparation and gel electrophoresis
- PCR (Taq, Vent)
- PCR product clean-up
- Enzyme digestion (vector, insert)
- Plasmid DNA extraction
- Gel cutting
- Gel extraction
- Ethanol precipitation
- Ligation
- Transformation to E.coli
- Transformation to yeast
- Cell lysis
- Yeast genomic DNA extraction
- Western blotting
- GFP testing