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| DNA Techniques Post questions and discuss DNA techniques and protocols such as DNA extraction, PCR, and the study of DNA-binding proteins. |
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#1
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| Hey guys, I have a problem. Some bands on my gel are too close together. Is there a way I can cut them? Should I re run the gel? I dont want to waste my DNA... ![]() thanks again DNAmolecule |
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#2
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| Rerun the gel and extend the time for a bit longer. If your time was 30min try 40min..etc |
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#3
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| After you´ve seen your gel on UV, you can ever re run your gel untill you want..... there are not ploblems to do this!!!! |
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#4
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| Or increase the Agarose percentage. |
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#5
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| I´ve found that a long 3% agarose gel separates most closely migrating bands. I´ve been able to separate a pair of 500 and 520 bp bands in this way. Try to run the gel for as long as you can. Good luck! Irideus |
| The Following User Says Thank You to Irideus For This Useful Post: | ||
admin (06-07-2011)
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#6
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| If you have access to acrilamyde and bisacrilamyde, prepare a polyacrilamyde gel, a 6% gel can separate a fragment of 6 bp difference (ie. 112 bp and 106 bp). If you are interested I can give you some pointers about it. Just let me know. |
| The Following User Says Thank You to luisillo For This Useful Post: | ||
admin (06-07-2011)
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| Tags |
| agarose , bands , close , dna , gel |
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| Thread | Thread Starter | Forum | Replies | Last Post |
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