Team:HKUST/Protocols/Agarose gel

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1. Agarose gel preparation and gel electrophoresis
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<link href="http://igem2009hkust.fileave.com/wiki/template/12092009/style.css " rel="stylesheet" type="text/css" />
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<title>Salt and Soap template</title>
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</head>
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*Purpose: To check the result
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*Materials: Agarose, 0.5X TBE, SYBR safe DNA gel stain, DNA loading dye, DNA ladder/marker  
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**Choice of ladders: VC100bp Plus DNA ladder (highest band 3000bp); Lamda DNA BstEII marker (highest band 8400bp, 1% argarose)
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<div id="headerxx">
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*Procedure:  
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**To make a 0.8% agarose gel, use 0.16 g agarose per 20 mL 0.5x TBE.  
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</div>
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**Cover the flask with plastic wrap to prevent boiling over, then microwave the solution for 1-2 minutes to  dissolve the agarose.  
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<div id="borderxx">
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**Let agarose solution cool for 5 minutes, then add SYBR safe DNA gel stain to a final concentration of 0.5 μg/mL.  
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<div id="mainxx">
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**Pour the agarose solution into a casting tray with well comb in place. Allow 20-30 minutes to completely solidify.
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<div id="leftxx">
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**Place the agarose gel into the gel box and fill the box with 0.5X TBE until the gel is immersed.
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<div id="menuxx">
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**Load an appropriate molecular weight ladder into the first lane of the gel. If needed, an additional ladder with different molecular weight could be loaded into the last lane.
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<ul>
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**Add 1 μL loading dye per 5 μL of sample.
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<li><a href="https://2009.igem.org/Team:HKUST">Home</a></li>
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**Load the samples from left to right.
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<li><a href="https://2009.igem.org/Team:HKUST/Team">Our Team</a></li>
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**Cover the gel box and plug in the electrodes in a way that the samples will run towards the positive, red electrode.
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<li><a href="https://2009.igem.org/Team:HKUST/Project">Project Description</a></li>
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**Run the gel at 100V until the dye line is approximately 50-75% of the way down the gel. Approximately 20-30 minutes.
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**Carefully remove the gel from the gel box and check the result under UV exposure.
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<b>
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*Tips:  
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<span style="color:green">
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**Higher concentration of agarose solution makes better resolution for less molecular weight expected band.
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<li>Main Parts</li>
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**Let bottom of the flask be immersed in a cup of cold water for faster cooling.
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</span>
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**In order for clearer band to cut specific band on the gel, immerse the gel in Ethidium bromide for 10-15 minutes after step k.
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</b>
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*Safety tips:  
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<li><a href="https://2009.igem.org/Team:HKUST/OdorantSensing">Odorant Sensing</a></li>
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**Be sure to wear a glove before treating the hot flask.
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<li><a href="https://2009.igem.org/Team:HKUST/AttractantProduction">Attractant Production</a></li>
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**Ethidium bromide is a strong mutagen. Wear a lab coat, eye protection, and gloves when working with this chemical.
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<li><a href="https://2009.igem.org/Team:HKUST/ToxinProduction">Toxin Production</a></li>
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<b>
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<span style="color:green">
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<li>Resources</li>
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</span>
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</b>
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<li><a href="https://2009.igem.org/Team:HKUST/Lab Notebook">Lab Notebook</a></li>
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<li><a href="https://2009.igem.org/Team:HKUST/Parts">Parts Submitted </a></li>
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<li><a href="https://2009.igem.org/Team:HKUST/Protocols">Protocol List</a></li>
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<li><a href="https://2009.igem.org/Team:HKUST/Resourses">Other Resources</a></li>
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</ul>
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</div>
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<div id="menubottom">
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<ul>
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<li><a href="https://2009.igem.org/Team:Gallery">Gallery</a></li>
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<li><a href="https://2009.igem.org/Team:Biosafety">Biosafety</a></li>
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<li><a href="https://2009.igem.org/Team:Acknowledgement">Acknowledgement</a></li>
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</ul>
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</div>
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</div>
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<div id="rightxx">
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<div class="contentlist"> <h3>a</h3>
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</div>
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<div class="contentxx">
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<p>Agarose gel preparation and gel electrophoresis</p>
 +
 
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<p> Purpose: To check the result </p>
 +
Materials: Agarose, 0.5X TBE, SYBR safe DNA gel stain, DNA loading dye, DNA ladder/marker <br><br>
 +
Choice of ladders: VC100bp Plus DNA ladder (highest band 3000bp); Lamda DNA BstEII marker (highest band 8400bp, 1% argarose) <br><br>
 +
 
 +
<p>Procedure: </p>
 +
1. To make a 0.8% agarose gel, use 0.16 g agarose per 20 mL 0.5x TBE. <br>
 +
2. Cover the flask with plastic wrap to prevent boiling over, then microwave the solution for 1-2 minutes to  dissolve the agarose. <br>
 +
3. Let agarose solution cool for 5 minutes, then add SYBR safe DNA gel stain to a final concentration of 0.5 μg/mL. <br>
 +
4. Pour the agarose solution into a casting tray with well comb in place. Allow 20-30 minutes to completely solidify.<br>
 +
5. Place the agarose gel into the gel box and fill the box with 0.5X TBE until the gel is immersed.<br>
 +
6. Load an appropriate molecular weight ladder into the first lane of the gel. If needed, an additional ladder with different molecular weight could be loaded into the last lane.<br>
 +
7. Add 1 μL loading dye per 5 μL of sample.<br>
 +
8. Load the samples from left to right.<br>
 +
9. Cover the gel box and plug in the electrodes in a way that the samples will run towards the positive, red electrode.<br>
 +
10. Run the gel at 100V until the dye line is approximately 50-75% of the way down the gel. Approximately 20-30 minutes.<br>
 +
11. Carefully remove the gel from the gel box and check the result under UV exposure.<br>
 +
<p> Tips: </p>
 +
A. Higher concentration of agarose solution makes better resolution for less molecular weight expected band.<br>
 +
B. Let bottom of the flask be immersed in a cup of cold water for faster cooling.<br>
 +
C. In order for clearer band to cut specific band on the gel, immerse the gel in Ethidium bromide for 10-15 minutes after step k.<br>
 +
<p> Safety tips: </p>
 +
1. Be sure to wear a glove before treating the hot flask.<br><br>
 +
2. Ethidium bromide is a strong mutagen. Wear a lab coat, eye protection, and gloves when working with this chemical. <br><br>
 +
 
 +
<ul>
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<li><a href="https://2009.igem.org/Team:HKUST/Protocols/Agarose_gel" >Agarose gel preparation and gel
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electrophoresis</a></li>
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<li><a href="https://2009.igem.org/Team:HKUST/Protocols/PCR">PCR (Taq, Vent)</a></li>
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<li><a href="https://2009.igem.org/Team:HKUST/Protocols/PCR_cleanup">PCR product clean-up</a></li>
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<li><a href="https://2009.igem.org/Team:HKUST/Protocols/Enzyme_digestion"> Enzyme digestion (vector, insert)</a></li>
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<li><a href="https://2009.igem.org/Team:HKUST/Protocols/plasmid_extraction"> Plasmid DNA extraction</a></li>
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<li><a href="https://2009.igem.org/Team:HKUST/Protocols/gel_cut"> Gel cutting</a></li>
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<li><a href="https://2009.igem.org/Team:HKUST/Protocols/gel_extraction"> Gel extraction</a></li>
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<li><a href="https://2009.igem.org/Team:HKUST/Protocols/Ethanol_precipitation"> Ethanol precipitation</a></li>
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<li><a href="https://2009.igem.org/Team:HKUST/Protocols/Ligation"> Ligation</a></li>
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<li><a href="https://2009.igem.org/Team:HKUST/Protocols/Transformation_to_Ecoli"> Transformation to E.coli</a></li>
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<li><a href="https://2009.igem.org/Team:HKUST/Protocols/Transformation_to_yeast">Transformation to
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yeast</a></li>
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<li><a href="https://2009.igem.org/Team:HKUST/Protocols/Cell_lysis"> Cell lysis</a></li>
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<li><a href="https://2009.igem.org/Team:HKUST/Protocols/Yeast_genomic_DNA_extraction"> Yeast genomic DNA
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extraction</a></li>
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<li><a href="https://2009.igem.org/Team:HKUST/Protocols/Western_blotting"> Western blotting</a></li>
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<li><a href="https://2009.igem.org/Team:HKUST/Protocols/GFP_testing"> GFP testing</a></li>
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</ul>
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</div>
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<div class="productxx">
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<div class="clear"></div>
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</div>
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</div>
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<div class="clear"></div>
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</div>
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</div>
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<div id="footerxx">
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<div id="copyright">
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<span> iGEM 2009 <br /> </span>
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</div>
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<div id="payment"><img src="http://igem2009hkust.fileave.com/wiki/template/12092009/images/HKUSTLogo.jpg" alt="HKUST" /></div>
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</div>
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<div id="footerend"></div>
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</div>
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</bodyxx>
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</html>

Latest revision as of 09:54, 20 October 2009

Salt and Soap template

a

Agarose gel preparation and gel electrophoresis

Purpose: To check the result

Materials: Agarose, 0.5X TBE, SYBR safe DNA gel stain, DNA loading dye, DNA ladder/marker

Choice of ladders: VC100bp Plus DNA ladder (highest band 3000bp); Lamda DNA BstEII marker (highest band 8400bp, 1% argarose)

Procedure:

1. To make a 0.8% agarose gel, use 0.16 g agarose per 20 mL 0.5x TBE.
2. Cover the flask with plastic wrap to prevent boiling over, then microwave the solution for 1-2 minutes to dissolve the agarose.
3. Let agarose solution cool for 5 minutes, then add SYBR safe DNA gel stain to a final concentration of 0.5 μg/mL.
4. Pour the agarose solution into a casting tray with well comb in place. Allow 20-30 minutes to completely solidify.
5. Place the agarose gel into the gel box and fill the box with 0.5X TBE until the gel is immersed.
6. Load an appropriate molecular weight ladder into the first lane of the gel. If needed, an additional ladder with different molecular weight could be loaded into the last lane.
7. Add 1 μL loading dye per 5 μL of sample.
8. Load the samples from left to right.
9. Cover the gel box and plug in the electrodes in a way that the samples will run towards the positive, red electrode.
10. Run the gel at 100V until the dye line is approximately 50-75% of the way down the gel. Approximately 20-30 minutes.
11. Carefully remove the gel from the gel box and check the result under UV exposure.

Tips:

A. Higher concentration of agarose solution makes better resolution for less molecular weight expected band.
B. Let bottom of the flask be immersed in a cup of cold water for faster cooling.
C. In order for clearer band to cut specific band on the gel, immerse the gel in Ethidium bromide for 10-15 minutes after step k.

Safety tips:

1. Be sure to wear a glove before treating the hot flask.

2. Ethidium bromide is a strong mutagen. Wear a lab coat, eye protection, and gloves when working with this chemical.

HKUST

Retrieved from "http://2009.igem.org/Team:HKUST/Protocols/Agarose_gel"