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Team:Wageningen UR/Journal/week25
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* transformation of BBa_K883702 with BL21 (producing strain) - plating the transformants on plates containing IPTG | * transformation of BBa_K883702 with BL21 (producing strain) - plating the transformants on plates containing IPTG | ||
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''19 October'' | ''19 October'' | ||
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-> all the colonies picked had the correct insert and showed fluorescence under the UV light | -> all the colonies picked had the correct insert and showed fluorescence under the UV light | ||
| + | [[File:Gfpcoil in bl21.png|500px|center|thumb|<p align="justify">''Figure 3: the transformation was successful since all the colonies on the plate show slight green fluorescence.'</p>]] | ||
[[File:Colony pcr gfpcoilhis tag .png|500px|center|thumb|<p align="justify">''Figure 4: the colony PCR shows that all picked colonies had the correct insert size. Bba_I13522 was used as a positive control and reference.'</p>]] | [[File:Colony pcr gfpcoilhis tag .png|500px|center|thumb|<p align="justify">''Figure 4: the colony PCR shows that all picked colonies had the correct insert size. Bba_I13522 was used as a positive control and reference.'</p>]] | ||
Revision as of 10:47, 24 October 2012
Week 25: 15 october - 21 october
15 October
- 3rd time growing JM109 containing our biobricks BBa_K883702 (GFP coil with an IPTG induced promoter) and BBa_K883703 (GFP coil + His tag with an IPTG induced promoter) and induce expression with IPTG with new medium
-> no GFP production could be seen
16 October
- to check if there are any colonies showing green fluorescence on the original plate (of the transformation on 21.September GFPcoil; GFPcoil + his tag in Bba_J04500 (IPTG induced promoter) in JM109), colonies where picked randomly and plated on agarplates containing IPTG next to the selection antibiotic
-> some colonies containing GFPcoil with an IPTG induced promoter show green fluorescence
Figure 1: 3 colonies containing GFPcoil with an IPTG induced promoter show a slight green colour in normal daylight'
- plate the JM109 samples that where used for sending the bricks in to the registry - containing BBa_K883702(GFPcoil with IPTG induced promoter) and BBa_K883703 (GFPcoil + His tag with IPTG induced promoter) on agarplates containing IPTG next to the selection antibiotic
-> culture containing BBa_K883702(GFPcoil with IPTG induced promoter) shows green fluorescence
Figure 2: BBa_K883702(GFPcoil with IPTG induced promoter)in JM109 [left] shows some green fluorescence whereas for BBa_K883703 (GFPcoil + His tag with IPTG induced promoter) in JM109 [right] no fluorescence can be seen '
- grow colonies containing the biobricks BBa_K883702 BBa_K883703 BBa_K883701 and BBa_K883700
- grow colonies containing BBa_K883702 and BBa_K883703 in duplo once with IPTG in the medium and once adding IPTG (fresh stock solution) to the culture at OD=0.6
- miniprep of the colonies containing BBa_K883702 BBa_K883703 BBa_K883701 and BBa_K883700
- 2nd try to send the bricks BBa_K883702 BBa_K883703 BBa_K883701 and BBa_K883700 in for sequencing
-> sequencing revealed that BBa_K883702 and BBa_K883703 had the expected sequence but BBa_K883701 and BBa_K883700 where faulty - therefore we deleted these two bricks from the registry
18 October
- transformation of BBa_K883702 with BL21 (producing strain) - plating the transformants on plates containing IPTG
19 October
- colony PCR of the transformation BBa_K883702 with BL21 using sequencing primers and plating the picked colonies again on a plate containing IPTG
-> all the colonies picked had the correct insert and showed fluorescence under the UV light
Figure 3: the transformation was successful since all the colonies on the plate show slight green fluorescence.'
Figure 4: the colony PCR shows that all picked colonies had the correct insert size. Bba_I13522 was used as a positive control and reference.'
- checking fluorescence of the transformants on the IPTG containing plate under the UV light
Hepatitis B inside modification
15 October
- PCR check of the PCR fragment obtained on 27.August
Figure 5: The purified PCR fragment contains fragments of the correct size as well as a bigger fragment. The nonpurified sample shows only a smere.'
- ligation of the PCR product in pJET
- transformation with DH5α
-> there was growth on the negative control plate
