Richard Lab:Restriction Digest: Difference between revisions
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<center> | |||
'''This protocol is for the typical digestion of DNA done for [[Richard Lab:Amplified Insert Assembly|Amplified Insert Assembly]]. | |||
'''The [[Engineering BioBrick vectors from BioBrick parts/Restriction digest | consensus digestion protocol]] should be consulted if deviating from the procedure outlined here.'''</center> | |||
==Overview== | ==Overview== | ||
This protocol is typically used to do bio-brick digests with the restriction sites consisting of the following configuration: | This protocol is typically used to do bio-brick digests with the restriction sites consisting of the following configuration: | ||
<center>'''-----EcoRI--XbaI--Part--SpeI--PstI-----'''</center> | <center>'''-----EcoRI--XbaI--Part--SpeI--PstI-----'''</center> | ||
See the biobrick assembly schedule for more information on using this technique. | |||
==Materials== | ==Materials== | ||
| Line 8: | Line 14: | ||
* Restriction Endonucleases | * Restriction Endonucleases | ||
** With corresponding 10X buffer. NEBuffer 2 can be used for most applications but check [http://www.neb.com/nebecomm/tech_reference/restriction_enzymes/buffer_activity_restriction_enzymes.asp? this chart] to be sure. | ** With corresponding 10X buffer. NEBuffer 2 can be used for most applications but check [http://www.neb.com/nebecomm/tech_reference/restriction_enzymes/buffer_activity_restriction_enzymes.asp? this chart] to be sure. | ||
* BSA | * BSA | ||
* Phosphatase | * Antarctic Phosphatase | ||
*Distilled water | * Distilled water | ||
==Procedure== | ==Procedure== | ||
1. Quickly vortex all ingredients (Buffer, BSA, DNA) before beginning. | |||
2. Add the following in a micro-centrifuge tube: | |||
::*5μl of Buffer (usually NEBuffer 2); | |||
::*1μl of BSA; | |||
::*0.5 picomoles DNA (see [[DNA Quantification]]);[[user:Michael A. Speer | Mike]] normally uses 10μL of miniprep or 5μL of purified PCR product. | |||
::*Water to make 48μl. | |||
3. Vortex Enzymes and add 1μl of each to the tube. | |||
::*If you're digesting purified PCR product (i.e. "insert"), add 1μl of DpnI to the reaction. | |||
4. Incubate reaction in a 37°C water bath for at least one hour. | |||
::*If your digesting a "vector", add 1μl Antarctic Phosphatase and 6μl of Phosphatase buffer after 2 hours of incubation and incubate for another hour. | |||
::*See the [[Richard Lab:Bio-Brick Assembly Schedule|Bio-Brick Assembly Schedule]] for more details. | |||
5. Heat kill the digests for 20 minutes at 80°C. | |||
6. Store digested DNA in the refrigerator (4°C)for use in the very near future. | |||
==Notes== | ==Notes== | ||
Please feel free to post comments, questions, or improvements to this protocol. Happy to have your input! | Please feel free to post comments, questions, or improvements to this protocol. Happy to have your input! | ||
*DpnI eliminates the background from your PCR template | |||
*Antarctic Phosphatase eliminates background from the vector self ligating. | |||
*If you're not getting good digestion it might be because your enzyme is bad. Double the digestion time and see. | *If you're not getting good digestion it might be because your enzyme is bad. Double the digestion time and see. | ||
*Longer digest gives more complete digestion, especially if you have >1µg of DNA, but can sometimes give nonspecific digestion | *Longer digest gives more complete digestion, especially if you have >1µg of DNA, but can sometimes give nonspecific digestion | ||
*Beware the the NEB double digest chart. For EcoRI and PstI double digest it recommends using the EcoRI NEBuffer. However based on my digests both NEBuffer 2 and 3 work better; with NEBuffer 2 giving the most complete double digestion. It is funny that | *Beware the the NEB double digest chart. For EcoRI and PstI double digest it recommends using the EcoRI NEBuffer. However based on my digests both NEBuffer 2 and 3 work better; with NEBuffer 2 giving the most complete double digestion. It is funny that they recommend the EcoRI buffer because their chart also says that PstI is only 50% active in that buffer. | ||
==References== | ==References== | ||
| Line 38: | Line 49: | ||
or instead, [[Talk:{{PAGENAME}}|discuss this protocol]]. | or instead, [[Talk:{{PAGENAME}}|discuss this protocol]]. | ||
==BioCoder version== | |||
Following is the Richard Lab:Restriction Digest 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]] | |||
====Text Output==== | |||
[[Richard Lab:Restriction Digest protocol]] | |||
====Source Code==== | |||
[[Richard Lab:Restriction Digest protocol - source code]] | |||
[[Category:Protocol]] [[Category:DNA]] [[Category:In vitro]] | [[Category:Protocol]] [[Category:DNA]] [[Category:In vitro]] | ||
Back to [[Richard_Lab:protocols | Protocols]] | Back to [[Richard_Lab:protocols | Protocols]] | ||
Latest revision as of 12:05, 29 March 2011
Back to Protocols
This protocol is for the typical digestion of DNA done for Amplified Insert Assembly.
The consensus digestion protocol should be consulted if deviating from the procedure outlined here.Overview
This protocol is typically used to do bio-brick digests with the restriction sites consisting of the following configuration:
See the biobrick assembly schedule for more information on using this technique.
Materials
- Prepared DNA from miniprep, PCR, or Gel Extraction
- Restriction Endonucleases
- With corresponding 10X buffer. NEBuffer 2 can be used for most applications but check this chart to be sure.
- BSA
- Antarctic Phosphatase
- Distilled water
Procedure
1. Quickly vortex all ingredients (Buffer, BSA, DNA) before beginning. 2. Add the following in a micro-centrifuge tube:
- 5μl of Buffer (usually NEBuffer 2);
- 1μl of BSA;
- 0.5 picomoles DNA (see DNA Quantification); Mike normally uses 10μL of miniprep or 5μL of purified PCR product.
- Water to make 48μl.
3. Vortex Enzymes and add 1μl of each to the tube.
- If you're digesting purified PCR product (i.e. "insert"), add 1μl of DpnI to the reaction.
4. Incubate reaction in a 37°C water bath for at least one hour.
- If your digesting a "vector", add 1μl Antarctic Phosphatase and 6μl of Phosphatase buffer after 2 hours of incubation and incubate for another hour.
- See the Bio-Brick Assembly Schedule for more details.
5. Heat kill the digests for 20 minutes at 80°C. 6. Store digested DNA in the refrigerator (4°C)for use in the very near future.
Notes
Please feel free to post comments, questions, or improvements to this protocol. Happy to have your input!
- DpnI eliminates the background from your PCR template
- Antarctic Phosphatase eliminates background from the vector self ligating.
- If you're not getting good digestion it might be because your enzyme is bad. Double the digestion time and see.
- Longer digest gives more complete digestion, especially if you have >1µg of DNA, but can sometimes give nonspecific digestion
- Beware the the NEB double digest chart. For EcoRI and PstI double digest it recommends using the EcoRI NEBuffer. However based on my digests both NEBuffer 2 and 3 work better; with NEBuffer 2 giving the most complete double digestion. It is funny that they recommend the EcoRI buffer because their chart also says that PstI is only 50% active in that buffer.
References
For more information you can check out the other restriction digest protocols.
Contact
or instead, discuss this protocol.
BioCoder version
Following is the Richard Lab:Restriction Digest 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
Richard Lab:Restriction Digest protocol
Source Code
Richard Lab:Restriction Digest protocol - source code
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