Team:Newcastle/24 August 2010

From 2010.igem.org

(Difference between revisions)
(Single digestion of pSB1C3)
(Single and Double Digestion of pGFPrrnB with yneA)
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The concentration ranged from 286.1 µl/ml to 518.7 µl/ml. Therefore we have obtained high concentration of ''yneA'' in pGFPrrnB.
The concentration ranged from 286.1 µl/ml to 518.7 µl/ml. Therefore we have obtained high concentration of ''yneA'' in pGFPrrnB.
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=Single and Double Digestion of pGFPrrnB with ''yneA''=
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=Single and Double Digestion of pGFPrrnB with filamentous cell part=
==Aims==
==Aims==
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The aim of this experiment is to check if the insert ''yneA'' has been inserted into vector pGFPrrnB.
+
The aim of this experiment is screen our minipreps to check if the insert is present.
==Materials and Protocol==
==Materials and Protocol==

Revision as of 00:54, 28 October 2010

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Contents

Miniprep for pGFPrrnB with filamentous cell part

Aims

The aim of this experiment is to obtain stock of the filamentous cell part in pGFP-rrnB for transformation into Bacillus subtilis 168.

Materials and Protocol

Please refer to qiagen minipreps and nanodrop spectrophotometer protocols.

Results

Tube 1 Tube 2 Tube 3 Tube 4 Tube 5 Tube 6 Tube 7 Tube 8 Tube 9 Tube 10 Tube 11 Tube 12
286.1 µl/ml 304.0 µl/ml 316.3 µl/ml 421.6 µl/ml 518.7 µl/ml 460.1 µl/ml 370.1 µl/ml 377.3 µl/ml 346.0 µl/ml 347.4 µl/ml 202.8 µl/ml 307.4 µl/ml

Table 1: Nanodrop spectrophotometer results. Table represents the amount of plasmid present in µl/ml quantity.

Discussion

The concentration ranged from 286.1 µl/ml to 518.7 µl/ml. Therefore we have obtained high concentration of yneA in pGFPrrnB.

Single and Double Digestion of pGFPrrnB with filamentous cell part

Aims

The aim of this experiment is screen our minipreps to check if the insert is present.

Materials and Protocol

We are doing two digests for pGFPrrnB and yneA:

  • Single digest with HindIII;
  • Double digest with EcoRI and NheI.


Please refer to restriction digests and gel electrophoresis.

Discussion

Gel electrophoresis will be done on the 25th August, 2010.