Team:Newcastle/26 August 2010
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- | == | + | ==Restriction Digest== |
===Aim=== | ===Aim=== | ||
- | To digest the PCR products of pSB1C3 and ''yneA'' from PCR purification. | + | To digest the PCR products of pSB1C3 and ''yneA'' from PCR purification with enzymes EcoR1 and Nhe1. |
===Materials and Protocol=== | ===Materials and Protocol=== | ||
Please refer to [[Team:Newcastle/Restriction_digests|restriction digest]]. | Please refer to [[Team:Newcastle/Restriction_digests|restriction digest]]. | ||
- | |||
==Gel extraction== | ==Gel extraction== |
Revision as of 11:20, 31 August 2010
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Contents |
yneA
PCR (Repeat)
Aim
To repeat the PCR that we did yesterday using the correct rocF primers.
Materials and Protocol
Please refer to PCR.
PCR Purification
Aim
To remove unwanted primers, taq polymerase, buffer and salts to obtain pure DNA.
Materials and Protocol
Please refer to PCR purification.
Restriction Digest
Aim
To digest the PCR products of pSB1C3 and yneA from PCR purification with enzymes EcoR1 and Nhe1.
Materials and Protocol
Please refer to restriction digest.
Gel extraction
Aim
To purify the DNA of yneA and pSB1C3 by extracting the bands from the gel after running gel electrophoresis. Concentration of DNA is then checked with NanoDrop.
Materials and Protocol
Please refer to:
Results
The gel did not show any band when we looked at it from GelDoc.
Conclusion
The restriction digest did not work, so we will repeat the protocol again tomorrow.