Team:Newcastle/26 August 2010

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Revision as of 11:02, 31 August 2010 by Deenatsu (Talk | contribs)

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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.


Digestion

Aim

To digest the PCR products of pSB1C3 and yneA from PCR purification.

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

When we look at the gel through the GelDoc, only pSB1C3 was successfully digested with EcoR1 and Pst1 while yneA did not show any bands.

Conclusion

We will repeat the protocol again on 31.08.10.



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