Name: f2INIp47g64149
Description: Fraction 2: comparison of C. elegans proteins from worms infected or not by the fungus Drechmeria coniospora
Version: MIAPE: Gel Electrophoresis 1.4
1. General features
1.1.1 Date Stamp
2008-07-15
1.1.2 Responsible person or role
Affiliation: Centre d'Immunologie de Marseille Luminy
(i) Name: Dr Jonathan Ewbank
(ii) Postal address: Research group of Innate immunity in C. elegans
Case 906
163 avenue de luminy
13288 Marseille Cedex 9
France
(iii) Email address: ewbank@ciml.univ-mrs.fr
1.1.3 Electrophoresis type
Two-Dimensional electrophoresis
2. Sample
2.1.1 Sample Name(s)
-
- Sample name: 25 µg of infected C. elegans proteins Cy3 labeled , 25 µg of naive C. elegans proteins Cy5 labeled , 25 µg internal standard Cy2 labeled
- Sample type: Test sample
-
- Sample name: 25 µg of infected C. elegans proteins Cy3 labeled , 25 µg of naive C. elegans proteins Cy5 labeled , 25 µg internal standard Cy2 labeled
- Sample type: Test sample
-
- Sample name: 25 µg of naive C. elegans proteins Cy3 labeled , 25 µg of infected C. elegans proteins Cy5 labeled , 25 µg internal standard Cy2 labeled
- Sample type: Test sample
-
- Sample name: 25 µg of naive C. elegans proteins Cy3 labeled , 25 µg of infected C. elegans proteins Cy5 labeled, 25 µg internal standard Cy2 labeled
- Sample type: Test sample
2.1.2 Loading buffer
- Urea 7M Thiourea 2M Chaps 4% ampholyte 1%
3. Gel matrix and electrophoresis protocol
3.1 Dimension details
3.1.1 Ordinal number for this dimension
First
3.1.2 Separation method employed
Isoelectric focusing (IEF)
3.2 Gel Matrix
3.2.1 Description of gel matrix
IPG strip
Denaturing
3.2.2 Gel manufacture
Gel was purchased precast.
Manufacturer: GE-healtcare
Model: ImmobilineTM DryStrip pH 4-7 linear 11 cm strips
Model number: 18-1016-60
Batch number: 64149-64150-64151-64152
3.2.3 Physical dimensions
X: 108 mm
Y: 3 mm
Z: 0.5 mm
3.2.4 Physiochemical property range and distribution
linear pH 4 - 7
3.2.5 Acrylamide concentration
4 %
3.2.6 Acrylamide : Crosslinker ratio
Crosslinker: Bisacrylamide
Ratio: 32:1
3.2.7 Additional substances in gel
Destreak rehydration solution: ref 17-6003-19 GE Healthcare
3.2.8 Gel lane
13.2.9 Sample application
Lane 1
- Sample: 25 µg of infected C. elegans proteins Cy3 labeled , 25 µg of naive C. elegans proteins Cy5 labeled , 25 µg internal standard Cy2 labeled
- Volume of sample: 75 µg
- Loading buffer: Urea 7M Thiourea 2M Chaps 4% ampholyte 1%
- Volume of loading buffer: 35 µL
Loading method: cup loading.
3.3 Protocol
3.3.1 Buffers
No buffer.
3.3.2 Electrophoresis conditions
Running temperature: 20 °C
Gradient: 0-30 V, 3 h
Gradient: 30-300 V, 3 h
Gradient: 300-8000 V, 8 h
Hold: 8000 V, 6 h
4. Inter-dimension Process
4.1 Protocol
4.1.1 Step name
equilibration
4.1.2 Inter dimension buffer
6 M Urea; 50 mM Tris-HCl pH 8,8; 34.5 %(v/v)Glycerol; 2 %(v/v)SDS; 65mM DTT; trace of Bromophenol blue
4.1.3 Additional reagents
No additional reagent.
4.1.4 Equipment
4.1.5 Protocol
Temperature: 20 °C.
Duration: 20 min.
Protocol:
20 minutes in equilibration buffer
3. Gel matrix and electrophoresis protocol
3.1 Dimension details
3.1.1 Ordinal number for this dimension
Second
3.1.2 Separation method employed
Sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE)
3.2 Gel Matrix
3.2.1 Description of gel matrix
slab gel
Denaturing
3.2.2 Gel manufacture
Gel was purchased precast.
Manufacturer: Bio-rad
Model: criterion XT bis-tris gel 10%
Model number: 3450115
Batch number: unknown
3.2.3 Physical dimensions
X: 133 mm
Y: 87 mm
Z: 1 mm
3.2.4 Physiochemical property range and distribution
logarithmic apparent molecular mass 10 - 250 kDa
3.2.5 Acrylamide concentration
10 %
3.2.6 Acrylamide : Crosslinker ratio
Crosslinker: Bisacrylamide
Ratio: 10:5
3.2.7 Additional substances in gel
No additional substance
3.2.8 Gel lane
13.2.9 Sample application
Loading method: well loading.
3.3 Protocol
3.3.1 Buffers
MOPS 1x
3.3.2 Electrophoresis conditions
Running temperature: 20 °C
Hold: 10 mA, 30 min
Hold: 30 mA, 30 min
Hold: 60 mA, 105 min
5. Detection
5.1 Direct detection
5.1.1 Name of direct detection_process
Fluorescent staining
5.1.2 Direct detection agents
GE Healtcare cy dye DIGE Fluor minimal labelling kit ref: 25-8010-65
Cy3, Cy5, Cy2 : 200 pmol cydye per sample
5.1.3 Additional reagents and buffers
DMF 100%
Lysine 10mmol
5.1.4 Equipment
No specialised equipment.
5.1.5 Direct detection protocol
Temperature: 4 °C.
Duration: 1 h.
Protocol:
Each Cy Dye is solved in 5 µl of 100% DMF as a stock solution. 1µl of the stock solution is diluted in 4µl of 100% DMF as the labelling solution. 1 µl of the Cy3 or the Cy5 Dye solution is added separatly to 25 µg protein of each "test" and each "control" sample. 4 µl of the Cy2 solution is added to the internal standard protein mixture, which contains 12.5 µg protein from each sample. Minimal labeling is done for 30 min at 4°C in the dark. Then, 1 µl of the lysine solution is added to each sample to stop the labeling reaction during 10 min still at 4°C in the dark. Each sample are combined according to the design experimental (see section 2.1.1), and DTT is added at a final concentration of 10 mmol for further 10 minutes at 4°C in the dark. The combined samples were supplemented with an equal volume of 2x sample buffer (8M urea, 2M thiourea, 4% (w/v) CHAPS, 1% (v/v) IPG Buffer 4-7 (GE Healthcare)
6. Image Acquisition
6.1 Acquisition Equipment
6.1.1 Type of equipment
fluorescent scanner6.1.2 Name of equipment
Manufacturer: GE-healtcare
Model: Ettan Dige Imager
Model number: 11-0036-58
6.1.3 Software
Manufacturer: GE-healtcare
Model: EDI software
Model number: 1.0
6.1.4 Calibration
Yes (automatic)
6.1.5 Equipment specific parameters
Excitation and emission filters combinations are automatically selected by the software:Cy2 excitation filter 480/30 nm and emission filter 530/40 nm
Cy3 excitation filter 540/25 nm and emission filter 595/25 nm
Cy5 excitation filter 635/30 nm and emission filter 680/25 nm
6.2 Acquisition Protocol
6.2.1 Image acquisition process
exposure time settingsgel1
0.6
0.2
0.4
gel2
1
0.4
0.6
gel3
1
0.7
0.35
gel4
0.8
0.5
0.3
6.2.2 Reference to gel matrix
There is only one gel in this document.
7. Image
7.1.1 Image name (or id)
f2inip47g64149 (format: JPEG)
7.1.2 Dimensions
Width: 1103 px
Height: 618 px
7.1.3 Resolution
100 µm/px
7.1.4 Bit-depth
24-bit (TrueColor)7.1.5 Image location
f2inip47g64149.jpg7.1.6 Standard image orientation
Yes