Team:Stockholm/18 October 2010

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Revision as of 14:53, 26 October 2010

Andreas

Transfer of ProtA⋅His to pEX

Digestion

	Sample
10X FastDigest buffer	1
Plasmid DNA	7
dH₂O	0
FD XbaI	1
FD PstI	1
	10 μl

Incubation: 37 °C, 0:30
Inactivation: 80 °C, 3:00

De-phosphorylated pre-digested/extracted pEX vector:

8 μl extracted and digested (X+P) pEX vector DNA
1 μl FD buffer
1 μl FastAP (alkaline phosphatase)

Incubation: 37 °C, 0:30
Inactivation: 80 °C, 3:00

Ligation

10X T4 Ligase buffer	2
Vector DNA	1
Insert DNA	11
dH₂O	5
T4 DNA ligase	1
	20 μl

Incubation: 22 °C, 1 h

Transformation

Including three more transformations

Modified quick-transformation protocol:

30 min on ice
50 μl BL21
1. 2 μl pEX.ProtA⋅his ligation mix
2. 0.5 μl pEX.IgGp
3. 0.5 μl pEX.SOD.RyC
4. 0.5 μl pEX.hS.RyC

PCR verification for Uppsala-Sweden team

Helping the Uppsala team with a PCR verification of one of their assemblies.

Summed up their total construct length in pSB1x3 to 6566 bp.

K1: C2 & C4 (x2)
K2: C2 & C5 (x2)

Standard colony PCR settings:

Elongation time: 10 min
Annealing temp: 55 °C and 60 °C

PCR run ON.

Nina

Polyacrylamide gel on SOD

I ran a polyacrylamide gel on SOD that I have tried to get pure.

Ladder: PageRuler Unst. Protein Ladder Fermentas

Arragement on gel:

I had a Coomassie blue staning and destaining on the gel.

Protein concentration

I measured the protein conc on the samples: unbound, wash 1-3, elute 1-4 and not pure to check if I had any proteins. I had to test this since the gel shows that I don't have any proteins, even not much in the unbound lane, which should have a lot of bands. It could also be that my samples that I loaded onto the gel was very diluted since I had fractions consisting of 10 ml solution. This could give me an indication wheter I need to concentrate my fractions with a Millipore centrifugation.

I measured the concentrations using a BSA-method.

I got a standard curve from another student (Annika) in the lab I work in.

The standard curve was obtained by following this:

I measured the conc by following these instructions:

I got these absorbance values for each well I loaded:

Samples from top to bottom: unbound, wash 1-3, elute 1-4.

From the standard curve I can calculate the protein concentration:

A = 0.3617 * C + 0.0778

C = (A-0.0778)/0.3617

However I realized that the blank I used did not have any imidazole added, this is therefore not a good control for the elute samples since they contain a high amount of imidazole.

The imidazole molecule contains structures that can absorbe light and therefore the value of the elute samples might only indicate the imidazole and not the protein conc in the sample.

Colony PCR

I PCR screened 16 colonies/dish of Protein A_LMWP_N, Protein A_TAT_N, Protein A_Tra10_N, Fusion_CPP1, Fusion_TAT_C & Fusion_CPP3.

The PCR protocol was according to previous ones where I added 25 ul PCR mix/PCR tube.

Elongation time for Protein A samples: 45 sec and for Fusion samples 2 min.

Mimmi

clone non-CPP operon

Gel

well	sample
1	ladder
2	pEX.SOD.his.RBS.yCCS 1
3	pEX.SOD.his.RBS.yCCS 2
4	pEX.SOD.his.RBS.yCCS 3
5	pEX.SOD.his.RBS.yCCS 4
6	pEX.SOD.his.RBS.yCCS 5
7	pEX.SOD.his.RBS.yCCS 6
8	pEX.SOD.his.RBS.yCCS 7