Team:Newcastle/24 August 2010

From 2010.igem.org

(Difference between revisions)
(Results)
(Results)
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*'''Lane 1''': 1 Kb ladder  
*'''Lane 1''': 1 Kb ladder  
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*'''Lane 2''': digested (linearised) pGFP-rrnB
+
*'''Lane 2''': digested (linearised) pSB1C3
==Discussion and Conclusion==
==Discussion and Conclusion==

Revision as of 01:17, 26 October 2010

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Contents

Miniprep for pGFPrrnB with yneA

Aims

To produce more stocks of vector pGFPrrnB with insert yneA.

Materials and Protocol

Please refer to qiagen minipreps and nanodrop spectrophotometer for all 12 tubes of miniprep that we did.

Results

The results from the nanodrop:

DNA Concentration (ng/µl)
1 286.1
2 304.0
3 316.3
4 421.6
5 518.7
6 460.1
7 370.1
8 377.3
9 346.0
10 347.4
11 202.8
12 307.4

Discussion

The results from the nanodrop showed that we have produced high concentration of vector pGFPrrnB with insert yneA. We will then proceed to digestion.

Single and Double Digestion of pGFPrrnB with yneA

Aims

To check if the insert yneA has been inserted into vector pGFPrrnB.

Materials and Protocol

We are doing two digests for pGFPrrnB and yneA:

  • Single digest with HinDIII;
  • Double digest with EcoR1 and Nhe1.


Please refer to restriction digests and gel electrophoresis.

Results

Gel electrophoresis results for digestion:

Discussion and Conclusion

Single digestion of pSB1C3

Aims

To linearise the vector pSB1C3. The linear vector will be used as a PCR template for Gibson cloning of the Subtilin immunity and rocF BioBricks.

Materials and Protocol

We are doing a single digest with HinDIII.

Please refer to restriction digests and gel electrophoresis.

Results

Gel electrophoresis results for digestion:

24.08.10.png

Figure 1: Gel electrophoresis of the amplified PCR products and restriction digest

  • Lane 1: 1 Kb ladder
  • Lane 2: digested (linearised) pSB1C3

Discussion and Conclusion

The digestion was successful — the correct band was seen. We can proceed to gel extraction.

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