Team:Newcastle/Labwork/30 September 2009

From 2009.igem.org


Team Newcastle 2009 iGEM ProbationaryP-Sign.PNG

Formal Lab Session - 30th September 2009

Chassis team

Introduction

  • Since we got the Midi Prep of kinA transformation, we have enough plasmid which are enought for digestion test. We take Chris's advice to use new ladder which would be more accurate in measuring DNA's size.


Experiment procedure

Digestion

  • Digestion reaction
 dd H2O                     7ul
 10X fast digest buffer     2ul
 Fast BamHI               0.5ul
 Fast HindIII             0.5ul
 Mini Prep DNA             10ul
 ------------------------------
                           20ul
  • K1: kinA midi result digested by EcoRI and NheI
  • K1: kinA midi result digested by HindIII
  • Other three digest sample came from Jess's mini prep for sac transformation.

Conclusion

  • Lane 3,4 were K1, K2 digested result. The kinA fragment is 2048bp, so the kinA band should be at the same position with the 6th band of lamda ladder or the 8th band of 1kb ladder. But the gel picture showed that those three bands were not at the same level. Even the ladder are not consist with each other. To confirm our kinA clone result, we need digested pMK-RQ as a standard control.


Team newcastle 2009 hanny geldoc 300909 kina.jpg


July
MTWTFSS
    1 2 3 4 5
6 7 8 9 10 11 12
13 14 15 16 17 18 19
20 21 22 23 24 25 26
27 28 29 30 31
August
MTWTFSS
          1 2
3 4 5 6 7 8 9
10 11 12 13 14 15 16
17 18 19 20 21 22 23
24 25 26 27 28 29 30
31
September
MTWTFSS
  1 2 3 4 5 6
7 8 9 10 11 12 13
14 15 16 17 18 19 20
21 22 23 24 25 26 27
28 29 30
October
MTWTFSS
      1 2 3 4
5 6 7 8 9 10 11
12 13 14 15 16 17 18
19 20 21 22 23 24 25
26 27 28 29 30 31



News

Events

Social Net

  • Newcastle iGEM Twitter
  • Newcastle on Facebook
  • Newcastle Youtube Channel