NanoBio: AgaroseGels: Difference between revisions
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You can make agarose from 0.5% to even 3%, by mass. 0.7% shows separation of large fragments (5-10kb) and 2% shows good separation of small fragments (0.2k-1k). Keep in mind the gelliness/solidness positively correlates with more agarose; 0.5% gel will be floppy and fragile. | You can make agarose from 0.5% to even 3%, by mass. 0.7% shows separation of large fragments (5-10kb) and 2% shows good separation of small fragments (0.2k-1k). Keep in mind the gelliness/solidness positively correlates with more agarose; 0.5% gel will be floppy and fragile. | ||
===Agarose % guide=== | |||
{| | |||
| Agarose (g/100mL) | |||
| DNA resolution (/kb) | |||
|- | |||
| 0.5 | |||
| 1-30 | |||
|- | |||
| 0.7 | |||
| 0.8-12 | |||
|- | |||
| 1.0 | |||
| 0.5-10 | |||
|- | |||
| 1.2 | |||
| 0.4-7 | |||
|- | |||
| 1.5 | |||
| 0.2-3 | |||
|} | |||
Taken from [[Agarose gel electrophoresis]]. | |||
==Ingredients== | ==Ingredients== | ||
Line 29: | Line 52: | ||
==References and Links== | ==References and Links== | ||
*[[Agarose gel electrophoresis]] | |||
*[http://www.biotechniques.com/article.asp?id=111199628 Gründemann, D and Schömig, E. BioTechniques 21:898-903 (November 1996)] | *[http://www.biotechniques.com/article.asp?id=111199628 Gründemann, D and Schömig, E. BioTechniques 21:898-903 (November 1996)] | ||
*[http://bitesizebio.com/2008/04/08/5-more-tips-for-dna-gel-extraction/ Enhancing gel extraction] | *[http://bitesizebio.com/2008/04/08/5-more-tips-for-dna-gel-extraction/ Enhancing gel extraction] | ||
*[http://www.methodbook.net/dna/agarogel.html Agarose gel electrophoresis] | *[http://www.methodbook.net/dna/agarogel.html Agarose gel electrophoresis] | ||
*[http://www.protocol-online.org/biology-forums/posts/18864.html TAE vs TBE] | *[http://www.protocol-online.org/biology-forums/posts/18864.html TAE vs TBE] |
Revision as of 13:43, 17 June 2008
Introduction
Agarose gels help you visualize DNA. Cool!
You can make agarose from 0.5% to even 3%, by mass. 0.7% shows separation of large fragments (5-10kb) and 2% shows good separation of small fragments (0.2k-1k). Keep in mind the gelliness/solidness positively correlates with more agarose; 0.5% gel will be floppy and fragile.
Agarose % guide
Agarose (g/100mL) | DNA resolution (/kb) |
0.5 | 1-30 |
0.7 | 0.8-12 |
1.0 | 0.5-10 |
1.2 | 0.4-7 |
1.5 | 0.2-3 |
Taken from Agarose gel electrophoresis.
Ingredients
- TAE or TBE, 1x - 50 mL is good for a little gel but you have to determine empirically
- Don't run a TAE gel in TBE
- Add extra volume of TAE to compensate for boiling
- If gel purifying: add 1 mmol/L guanosine to the TAE/TBE. This does not affect ligation and other downstream steps, however it will protect sticky ends. (See references)
- 0.5-2% agarose, by mass (e.g. for 1%, dissolve 0.5g agarose in 50 mL)
- Ethidium Bromide (for 10mg/mL, use 1uL per 50mL TAE)
Procedure
- Pour TAE into a flask that you can swirl to mix the contents
- Add agarose and swirl vigorously. It will be cloudy
- Microwave until it boils. Take it out and swirl (caution it's hot). Keep microwaving until the agarose flakes are minimized.
- Let it cool somewhere until around 50 C - to minimize EtBr vapours
- Add EtBr and swirl
- Pour into a gel tray and let it solidify
- Load samples and run gel.
How fast will my gel run?
Higher voltage and your DNA will migrate faster. It will also heat up the buffer⋛ don't melt it!
(Please add your own results too!)
- 1% agarose 50mL with Qiagen GelPilot 5x - orange <100bp band hits bottom ~20 minutes at 150V