Team:Groningen/Notebook/Wetwork 23July2012
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Tom and Arjan started with gas chromatography mass spectrometry. Test sample: 5gr. fresh meat incubated @ 37C for 3 houres. For both column (HP5 and CP wax) three runs on each column with different incubation and syringe temperature (1: 80C, 100C 2: 100C, 120C 3: 120C, 140C) | Tom and Arjan started with gas chromatography mass spectrometry. Test sample: 5gr. fresh meat incubated @ 37C for 3 houres. For both column (HP5 and CP wax) three runs on each column with different incubation and syringe temperature (1: 80C, 100C 2: 100C, 120C 3: 120C, 140C) | ||
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+ | Nisa | ||
+ | |||
+ | Plasmid isolation pSB1C3-alsT promoter + GFP | ||
+ | |||
+ | NanoDrop result (ng/ul): | ||
+ | |||
+ | A1= 102.9 | ||
+ | |||
+ | A2= 96,6 | ||
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+ | B1= 118,1 | ||
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+ | B2= 113,7 | ||
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+ | C1= 122,8 | ||
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+ | C2= 88 Comment: gel picture OK! | ||
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+ | D1= 124,9 | ||
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+ | D2= 93,3 | ||
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+ | |||
+ | Result: | ||
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+ | expected size: 3300bp for the pSB1C3 (2079bp)+ alsT (~500bp)+ GFP (800bp) | ||
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+ | From the gel picture, only plasmid from colony C2 (promoter alsT300) showed the expected size. The other plasmids seem to be empty, probably due to self ligation | ||
+ | |||
+ | Solution: Check plasmid from other white colony | ||
+ | |||
+ | redo transformation. Increase the ratio of plasmid backbone: insert gene |
Revision as of 13:41, 25 July 2012
Tom and Arjan started with gas chromatography mass spectrometry. Test sample: 5gr. fresh meat incubated @ 37C for 3 houres. For both column (HP5 and CP wax) three runs on each column with different incubation and syringe temperature (1: 80C, 100C 2: 100C, 120C 3: 120C, 140C)
Nisa
Plasmid isolation pSB1C3-alsT promoter + GFP
NanoDrop result (ng/ul):
A1= 102.9
A2= 96,6
B1= 118,1
B2= 113,7
C1= 122,8
C2= 88 Comment: gel picture OK!
D1= 124,9
D2= 93,3
Result:
expected size: 3300bp for the pSB1C3 (2079bp)+ alsT (~500bp)+ GFP (800bp)
From the gel picture, only plasmid from colony C2 (promoter alsT300) showed the expected size. The other plasmids seem to be empty, probably due to self ligation
Solution: Check plasmid from other white colony
redo transformation. Increase the ratio of plasmid backbone: insert gene