Lab notes (7/12 - 7/18)

Group: Flagella

Extraction of psb3k3 plasmids with incerted RFP from E. coli MG1655 (log phase)

Methods: MiniPrep, NanoDrop and gel electrophoresis

Notes: We used 9 ml ON culture, loaded 2ul sample and 8ul agarose loading dye on a 1,5% gel,used a DNA ladder mix (100-10000 nucleotides) as marker

Results: Nanodrop: Tube 1: 30.7 mg/ul Tube 2: 27.4 mg/ul

Gel electrophoresis: No result

--Louch07 15:00, 9 July 2010 (UTC)

Polyferation of FlhDC, FlhD and FlhC genes

Methods: PCR and Gel electrophoresis

Notes:Since our FldhDC primers have yet to work, we have decided to test them on previously purified cromosomal DNA. Examination of the primers showed that the FlhC reverse primer had a melting temperature of only 45˚C. Therefore we decided to run the samples on a gradient PCR. Simultaneously, we prepared 2 extra samples, isolating FlhD and FlhC, respectively. We did this because we wanted to see if our problems were caused because the combined gene-sequence was to long (932bp). Because we just wanted to test our primers in this PCR, we used Taq polymerase, because although it doesn’t proofread, it is remarkably cheaper than Pfu. On the [http://www.fermentas.com/en/products/all/pcr-qpcr-rt-pcr/standard-pcr/ep028-taq-dna-native Fermentas homepage] we found that the annealing temperature for Taq is Tm-5 , which in this case means 40˚C. However, Taq polymerase is not very effective at temperatures under 50˚C so we designed the gradient to lies between 40 and 55˚C. More specifically we chose the following temperatures:

Results: The experiment was succesfull! We could detect FlhDC DNA at temperatures between 42.6˚C and 48.3˚C. FlhD DNA at temperatures between 40.3˚C and 44.3˚C and also between 48.3˚C and 50.3˚C. FlhC DNA at temperatures run between 40.3˚C and 50.3˚C.

--Louch07 10:13, 12 July 2010 (UTC)

Group: Photosensor

Group: Retinal

Colony PCR of K274210 in pSB1A2 (transformation from 08/07)

Start date: 12/07 End date: 12/07
Methods: Colony PCR

Protocol: Modified iGEM colony PCR protocol

Notes: MgCl2 was added as a gradient,sample 1-2 contain 2 ul (0,04255), sample 3-5 2,25ul (0,04787). We mistakenly added 30ul (instead of 17ul) premix to sample 6 - 9, so the concentration of MgCl2 is reduced. Sample 6 contains 2,25ul (0,0375), Sample 7-8 2,5ul (0,04167), Sample 9 2,75ul (0,04583).

Gel was loaded with DNA-ladder plus, with the upper marker at 5000bp.

Results:
We found plasmids at the expected 5kbp marker in colonies 1-8.

Transformation of BBa_R0011 and BBa_I0500

Start date: 12/07 End date:
Methods: ON culture; Competent cells of E.Coli for transformation; Transformation of E.Coli.
Protocols: iGEM protocol for competent cells, iGEM protocol for transformation of E.Coli.


Experiment done by: Christian, Maria and LC (Making competent E.Coli)
Date: 12/07
Notes: Everything was done after protocol.
Results:
Analysis:


Experiment done by: Christian, Maria and LC (Transformation of pBad and lacl promoter)
Date: 12/07
Notes: Added 200ul of the un-pelleted cells, instead of 150ul to the agar plates.
Some of the agar dishes were damaged during drying and plating. We tried to use them anyways.

Results:
Analysis:

Mini-prep of pSB1A2 w. B0034, pSB1AK3 w. B0015 and pSB3K3 w. J04450(transformation from 08/07)

Start date: 12/07 End date: 12/07
Methods: Mini-prep (Fermentas)

Protocol: Fermentas protocol

Notes: pellet from 10 mL ON-culture was resuspended in 500uL resuspension buffer, and transferred into two eppendorf tubes, which were run in parellel

samples were loaded into a 1% gel with a gene ruler red marker.

Results:

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