DNA Precipitation

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(Procedure)
Current revision (05:43, 19 November 2009) (view source)
(BioStream version)
 
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# (Optional) Add 1 ml of 70% EtOH to the pellet and let sit for 5 minutes.
# (Optional) Add 1 ml of 70% EtOH to the pellet and let sit for 5 minutes.
# (Optional) Centrifuge the sample at maximum spped for 5 minutes.
# (Optional) Centrifuge the sample at maximum spped for 5 minutes.
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# (Optional)Decant and Discard the supernatant.
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# (Optional) Decant and Discard the supernatant.
# Air-dry the pellet for 10-15 minutes at room temperature until all liquid is gone.  
# Air-dry the pellet for 10-15 minutes at room temperature until all liquid is gone.  
# Resuspend in desired volume of water or buffer
# Resuspend in desired volume of water or buffer
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This protocol will precipitate all nucleic acids, not just DNA.  If you do not want RNA in your sample, one of the many ways to deal with it is to simply resuspend in TE + RNAse at the last step and leave it at room temperature for 15mins-1hr.
This protocol will precipitate all nucleic acids, not just DNA.  If you do not want RNA in your sample, one of the many ways to deal with it is to simply resuspend in TE + RNAse at the last step and leave it at room temperature for 15mins-1hr.
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==BioCoder version==
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Following is the DNA Precipitation protocol in BioCoder, a high-level programming language for expressing biology protocols. What you see here is the auto-generated text ouput of the protocol that was coded up in BioCoder (see Source code). More information about BioCoder can be found on my home page. Feel free to mail me your comments/ suggestions.[[User:Vaishnavi Ananth|Vaishnavi]]
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====Text Output====
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[[DNA Precipitation protocol]]
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====Source Code====
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[[DNA Precipitation protocol - source code]]
==References==
==References==

Current revision

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Contents

Overview

This protocol can be used to concentrate DNA, or to change the buffer the DNA is suspended in. It can also be coupled with phenol chloroform extraction for the purifying nucleic acids. This protocol also works for RNA precipitation (take care to use RNAse free materials in this case).

Materials

  • 3M NaOAc pH 5.2
  • EtOH 95%
  • Glycogen (optional)

Procedure

  1. Add 0.1 volumes of 3M Sodium Acetate solution to 1 volume of DNA sample.
  2. Add 1ul Glycogen to the DNA sample.
  3. Add 2 volumes of 95% EtOH to the DNA Sample.
  4. Store the solution overnight at -20°C or for 30 minutes at -80°C.
  5. Centrifuge the solution at maximum speed for least 15 minutes.
  6. Decant and discard the supernatant.
  7. (Optional) Add 1 ml of 70% EtOH to the pellet and let sit for 5 minutes.
  8. (Optional) Centrifuge the sample at maximum spped for 5 minutes.
  9. (Optional) Decant and Discard the supernatant.
  10. Air-dry the pellet for 10-15 minutes at room temperature until all liquid is gone.
  11. Resuspend in desired volume of water or buffer

Notes

-20°C for an hour is fine for using larger (1mL of bacterial culture, plasmid) amounts of DNA

The DNA pellet will not always be visible depending on how much DNA you are precipitating. So always take care in loading your samples in the centrifuge to remember the direction they are facing. The DNA pellet will be on the part of the tube facing the outside of the centrifuge.

This protocol will precipitate all nucleic acids, not just DNA. If you do not want RNA in your sample, one of the many ways to deal with it is to simply resuspend in TE + RNAse at the last step and leave it at room temperature for 15mins-1hr.

BioCoder version

Following is the DNA Precipitation protocol in BioCoder, a high-level programming language for expressing biology protocols. What you see here is the auto-generated text ouput of the protocol that was coded up in BioCoder (see Source code). More information about BioCoder can be found on my home page. Feel free to mail me your comments/ suggestions.Vaishnavi

Text Output

DNA Precipitation protocol

Source Code

DNA Precipitation protocol - source code

References

Links

Contact

Discuss this protocol.

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