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Latest revision as of 07:15, 20 November 2015
Labjournal Surchem September
Experiment 68a: Tetanus antigen on PDITC slides IX
- protocols used :Plasma activation, iRIf slide preparation
2015.09.16
Experiment/Protocol
- 4 PDITC slides were prepared
- Plasma activation: 40 L/h, 5 min
- APTES incubation: 30 min
- PDITC incubation: 2 h
- desiccator: 15 min
2015.09.16
Experiment/Protocol
Spotting pattern:
# | spot | Concentration |
---|---|---|
1 | pos. control (GFP) | 0.5 mg/ml |
2 | BSA | 5 mg/ml |
3 | Tetanus Antigen | ~0.5 mg/ml |
4 | pos. control (GFP) | 0.5 mg/ml |
5 | BSA | 5 mg/ml |
6 | Tetanus Antigen | ~0.5 mg/ml |
7 | pos. control (GFP) | 0.5 mg/ml |
8 | Tetanus Antigen | ~0.5 mg/ml |
* spots were incubated o/n at 4 °C
2015.09.17
Experiment/Protocol
Tet serum (-+): 024, 466
Reagent | Step | Flow rate (ul/min) | Priming time | Concentration |
---|---|---|---|---|
Buffer | 1 | 60 | 300 | 1x |
BSA | 2 | 60 | 600 | 10 mg/ml |
Buffer | 3 | 60 | 600 | 1x |
Serum(-) | 4 | 30 | 900 | 1:10 |
Buffer | 5 | 60 | 300 | 1x |
anti GFP | 6 | 30 | 900 | 1.5 µg/ml |
Buffer | 7 | 60 | 300 | 1x |
Serum(-) | 8 | 30 | 900 | 1:10 |
Buffer | 9 | 60 | 300 | 1x |
Tet serum (+-): 208, 216
Reagent | Step | Flow rate (ul/min) | Priming time | Concentration |
---|---|---|---|---|
Buffer | 1 | 60 | 300 | 1x |
BSA | 2 | 60 | 600 | 10 mg/ml |
Buffer | 3 | 60 | 600 | 1x |
Serum(-) | 4 | 30 | 900 | 1:10 |
Buffer | 5 | 60 | 300 | 1x |
anti GFP | 6 | 30 | 900 | 1.5 µg/ml |
Buffer | 7 | 60 | 300 | 1x |
Serum(+) | 8 | 30 | 900 | 1:10 |
Buffer | 9 | 60 | 300 | 1x |
GFP; Tet serum (-+): 287
Reagent | Step | Flow rate (ul/min) | Priming time | Concentration |
---|---|---|---|---|
Buffer | 1 | 60 | 300 | 1x |
BSA | 2 | 60 | 600 | 10 mg/ml |
Buffer | 3 | 60 | 600 | 1x |
anti GFP | 4 | 30 | 900 | 1.5 µg/ml |
Buffer | 5 | 60 | 300 | 1x |
Serum(-) | 6 | 30 | 900 | 1:10 |
Buffer | 7 | 60 | 300 | 1x |
Serum(+) | 8 | 30 | 900 | 1:10 |
Buffer | 9 | 60 | 300 | 1x |
Results
Serum(-),anti GFP,Serum(+):
]
Serum(+),anti GFP,Serum(-):
anti GFP,Serum(-),Serum(+):
Experiment 67b: Tetanus antigen on PDITC slides VIII
- protocols used :Plasma activation, iRIf slide preparation
2015.09.12
Experiment/Protocol
- 4 PDITC slides were prepared
- Plasma activation: 40 L/h, 5 min
- APTES incubation: 30 min
- PDITC incubation: 2 h
- desiccator: 15 min
2015.09.13
Experiment/Protocol
Spotting pattern:
# | spot | Concentration |
---|---|---|
1 | pos. control (GFP) | 0.5 mg/ml |
2 | BSA | 5 mg/ml |
3 | Tetanus Antigen | ~0.5 mg/ml |
4 | - | - |
5 | - | - |
6 | bBSA | 200 µg/ml |
* spots were incubated o/n at 4 °C
2015.09.14
Experiment/Protocol
Tet serum (-): 208, 254
Tet serum (+): 500, 024
Reagent | Step | Flow rate (ul/min) | Priming time | Concentration |
---|---|---|---|---|
Buffer | 1 | 60 | 600 | 1x |
BSA | 2 | 60 | 600 | 10 mg/ml |
Buffer | 3 | 60 | 600 | 1x |
anti-GFP | 4 | 30 | 600 | 1.5 ug/ml |
Buffer | 5 | 60 | 300 | 1x |
Serum SIG002 (-)/(+) | 6 | 30 | 900 | 1:20 |
Buffer | 7 | 60 | 300 | 1x |
Anti Human | 8 | 30 | 600 | 5 ug/ml |
Buffer | 9 | 60 | 300 | 1x |
StrepCy5 | 10 | 30 | 600 | 5 ug/ml |
Buffer | 11 | 60 | 300 | 1x |
Results
Blood Serum(-):
]
Blood serum(+):
Experiment 67a: Tetanus antigen on PDITC slides VII
- protocols used :Plasma activation, iRIf slide preparation
2015.09.12
Experiment/Protocol
- 4 PDITC slides were prepared
- Plasma activation: 40 L/h, 5 min
- APTES incubation: 30 min
- PDITC incubation: 2 h
- desiccator: 15 min
Spotting pattern:
# | spot | Concentration |
---|---|---|
1 | pos. control (GFP) | 0.5 mg/ml |
2 | BSA | 5 mg/ml |
3 | Tetanus Antigen | ~0.5 mg/ml |
4 | - | - |
5 | - | - |
6 | bBSA | 200 µg/ml |
* spots were incubated o/n at 4 °C
2015.09.13
Experiment/Protocol
Tet serum (-): 443, 466
Tet serum (+): 423, 424
Reagent | Step | Flow rate (ul/min) | Priming time | Concentration |
---|---|---|---|---|
Buffer | 1 | 60 | 600 | 1x |
BSA | 2 | 60 | 600 | 10 mg/ml |
Buffer | 3 | 60 | 600 | 1x |
anti-GFP | 4 | 30 | 600 | 1.5 ug/ml |
Buffer | 5 | 60 | 300 | 1x |
Serum SIG002 (-)/(+) | 6 | 30 | 900 | 1:10 |
Buffer | 7 | 60 | 300 | 1x |
Anti Human | 8 | 30 | 600 | 5 ug/ml |
Buffer | 9 | 60 | 300 | 1x |
StrepCy5 | 10 | 30 | 600 | 5 ug/ml |
Buffer | 11 | 60 | 300 | 1x |
Results
Blood Serum(-):
]
Blood serum(+):
Experiment 66b: PDITC slides for iRIf
- protocols used :Plasma activation, iRIf slide preparation
2015.09.06
Experiment/Protocol
- 6 PDITC slides were prepared
- Plasma activation: 40 L/h, 5 min
- APTES incubation: 30 min
- PDITC incubation: 2 h
- desiccator: 15 min
- stored at 4 °C
Experiment 66a: PDITC slides for iRIf
- protocols used :Plasma activation, iRIf slide preparation
2015.09.06
Experiment/Protocol
- 4 PDITC slides were prepared
- Plasma activation: 40 L/h, 5 min
- APTES incubation: 30 min
- PDITC incubation: 2 h
- desiccator: 15 min
- stored at 4 °C
2015.09.10
Experiment/Protocol
- slides were sandwiched with NTA and incubated at 4°C o/n
2015.09.10
Experiment/Protocol
- slides were blocked with APTES blocking solution for 1 h
- slides were washed 2x with PBS
- slides were incubated with NiSO4-solution for 1 h and 20 min
- slides were washed with PBS/2x diluted PBS
Experiment 65c: Tetanus antigen PDITC slides for iRIf VI
- protocols used :Plasma activation, iRIf slide preparation
2015.08.31
Experiment/Protocol
- 4 PDITC slides were prepared
- Plasma activation: 40 L/h, 5 min
- APTES incubation: 30 min
- PDITC incubation: 2 h
- desiccator: 30 min
- stored at 4 °C
2015.09.05
Experiment/Protocol
Spotting pattern:
# | spot | Concentration |
---|---|---|
1 | pos. control (GFP) | 0.5 mg/ml |
2 | BSA | 5 mg/ml |
3 | Tetanus Antigen | ~0.5 mg/ml |
4 | - | - |
5 | - | - |
6 | bBSA | 200 µg/ml |
2015.09.06
Experiment/Protocol
Flush protocol:
Tet serum (-): 443
Tet serum (+): 466
Reagent | Step | Flow rate (ul/min) | Priming time | Concentration |
---|---|---|---|---|
Buffer | 1 | 60 | 600 | 1x |
BSA | 2 | 60 | 600 | 10 mg/ml |
Buffer | 3 | 60 | 600 | 1x |
anti-GFP | 4 | 30 | 600 | 1.5 ug/ml |
Buffer | 5 | 60 | 300 | 1x |
Serum SIG002 (-)/(+) | 6 | 30 | 600 | 1:4 |
Buffer | 7 | 60 | 300 | 1x |
StrepCy5 | 8 | 30 | 600 | 5 ug/ml |
Buffer | 9 | 60 | 300 | 1x |
Tet serum (-): 208
Tet serum (+): 303
Reagent | Step | Flow rate (ul/min) | Priming time | Concentration |
---|---|---|---|---|
Buffer | 1 | 60 | 600 | 1x |
BSA | 2 | 60 | 600 | 10 mg/ml |
Buffer | 3 | 60 | 600 | 1x |
anti-GFP | 4 | 30 | 600 | 1.5 ug/ml |
Buffer | 5 | 60 | 300 | 1x |
Serum SIG002 (-)/(+) | 6 | 60 | 600 | 1:6 |
Buffer | 7 | 60 | 300 | 1x |
StrepCy5 | 8 | 30 | 600 | 5 ug/ml |
Buffer | 9 | 60 | 300 | 1x |
Note: the amount of flushed serum
Results
Blood Serum(-):
]
Blood serum(+):
→ for the blood serum after immunization (+) the iRIf signal for tetanus binding is higher than for the blood serum before immunization (-)
→ there are differences to the results of experiment 59a, the overall tetanus signal is much weaker as well as the binding of the blood serum to bBSA
Experiment 65b: Tetanus antigen PDITC slides for iRIf V
- protocols used :Plasma activation, iRIf slide preparation
2015.08.31
Experiment/Protocol
- 4 PDITC slides were prepared
- Plasma activation: 40 L/h, 5 min
- APTES incubation: 30 min
- PDITC incubation: 2 h
- desiccator: 30 min
2015.09.04
Experiment/Protocol
Spotting pattern:
# | spot | Concentration |
---|---|---|
1 | pos. control (GFP) | 0.5 mg/ml |
2 | BSA | 5 mg/ml |
3 | Tetanus Antigen | ~0.5 mg/ml |
4 | - | - |
5 | - | - |
6 | bBSA | 200 µg/ml |
2015.09.05
Experiment/Protocol
Flush protocol:
SIG 003 (+): 012(no serum was flushed over the slide), 315, 426
SIG 002 (+): 215
Reagent | Step | Flow rate (ul/min) | Priming time | Concentration |
---|---|---|---|---|
Buffer | 1 | 60 | 600 | 1x |
BSA | 2 | 60 | 600 | 10 mg/ml |
Buffer | 3 | 60 | 600 | 1x |
anti-GFP | 4 | 30 | 600 | 1.5 ug/ml |
Buffer | 5 | 60 | 300 | 1x |
Blood serum | 6 | 30 | 600 | 1:30 |
Buffer | 7 | 60 | 300 | 1x |
StrepCy5 | 8 | 30 | 600 | 5 ug/ml |
Buffer | 9 | 60 | 300 | 1x |
Results
SIG 003:
→ slide 012 was not flushed with any blood serum → for blood serum SIG 003 only a slight antigen/antibody binding is detectable (slide 426)
SIG 002:
→ slight antigen/antibody binding is detectable
→ no anti GFP/ GFP binding detected
→ only weak binding of the blood serum to bBSA → difference to results of experiment 59a
Experiment 65a: cell free GFP on NiNTA and PDITC slides for iRIf
- protocols used :Plasma activation, iRIf slide preparation
2015.08.31
Experiment/Protocol
- 2 PDITC slides were prepared (216,254)
- Plasma activation: 40 L/h, 5 min
- APTES incubation: 30 min
- PDITC incubation: 2 h
- desiccator: 30 min
- 2 Ni NTA slides from experiment 63b were also spotted (102,502)
2015.09.04
Experiment/Protocol
Spotting pattern:
# | spot | Concentration |
---|---|---|
1 | pos. control (GFP) | 0.5 mg/ml |
2 | cell free expression mix without DNA (KK) | |
3 | cell free expressed HA-GFP-His6-His6 (KK) | |
4 | pos. control (GFP) | 0.5 mg/ml |
5 | cell free expression mix without DNA (KK) | |
6 | cell free expressed His10-GFP-Spy (KK) | |
7 | BSA | 5 mg/ml |
8 | bBSA | 200 µg/ml |
2015.09.05
Experiment/Protocol
Flush protocol:
Reagent | Step | Flow rate (ul/min) | Priming time | Concentration |
---|---|---|---|---|
Buffer | 1 | 60 | 600 | 1x |
BSA | 2 | 60 | 600 | 10 mg/ml |
Buffer | 3 | 60 | 600 | 1x |
anti-GFP | 4 | 30 | 600 | 1.5 ug/ml |
Buffer | 5 | 60 | 300 | 1x |
StrepCy5 | 8 | 30 | 600 | 5 ug/ml |
Buffer | 9 | 60 | 300 | 1x |
Results
PDITC:
Ni-NTA:
→ the his tagged, cell free GFP was specificly bound by the Ni NTA surface, whereas there was no detectable amount of cell free GFP bound on the PDITC surfaces
→ the PDITC surface binds all proteins in the spotted cell free expression mix eaqually good, whereas the Ni-NTA surface specificly binds only the his tagged, cell free expressed GFP
Experiment 64c: Tetanus antigen PDITC slides for iRIf IV
- protocols used :Plasma activation, iRIf slide preparation
2015.08.31
Experiment/Protocol
- 4 PDITC slides were prepared
- Plasma activation: 40 L/h, 5 min
- APTES incubation: 30 min
- PDITC incubation: 2 h
- desiccator: 15 min
- stored at 4 °C
2015.09.03
Experiment/Protocol
Spotting pattern:
# | spot | Concentration |
---|---|---|
1 | pos. control (GFP) | 0.5 mg/ml |
2 | BSA | 5 mg/ml |
3 | Tetanus Antigen | ~0.5 mg/ml |
4 | - | - |
5 | mCherry | 0.5 mg/ml |
6 | bBSA | 200 µg/ml |
2015.09.04
Experiment/Protocol
Flush protocol:
Tet serum (-): 500(1:10 diluted serum)
Tet serum (+): 024 (1:10 diluted serum), 504 (1:30 diluted serum)
Reagent | Step | Flow rate (ul/min) | Priming time | Concentration |
---|---|---|---|---|
Buffer | 1 | 60 | 600 | 1x |
BSA | 2 | 60 | 600 | 10 mg/ml |
Buffer | 3 | 60 | 600 | 1x |
anti-GFP | 4 | 30 | 600 | 1.5 ug/ml |
Buffer | 5 | 60 | 300 | 1x |
Serum SIG002 (-)/(+) | 6 | 30 | 600 | 1:10/1:30 |
Buffer | 7 | 60 | 300 | 1x |
StrepCy5 | 8 | 30 | 600 | 5 ug/ml |
Buffer | 9 | 60 | 300 | 1x |
Results
Serum(-):
Serum(+):
→ bad measurement, no binding curves were obtained
→ signal for 1:10 dilution of the blood serum much better → continue with 1:10 dilution
Experiment 64b: Tetanus antigen PDITC slides for iRIf III
- protocols used :Plasma activation, iRIf slide preparation
2015.08.31
Experiment/Protocol
- 4 PDITC slides were prepared
- Plasma activation: 40 L/h, 5 min
- APTES incubation: 30 min
- PDITC incubation: 2 h
- desiccator: 15 min
- stored at 4 °C
2015.09.02
Experiment/Protocol
Spotting pattern:
# | spot | Concentration |
---|---|---|
1 | pos. control (GFP) | 0.5 mg/ml |
2 | mCherry | 0.5 mg/ml |
3 | Tetanus Antigen | ~0.5 mg/ml |
4 | BSA | 10 mg/ml |
5 | BSA +bBSA | 10 mg/ml |
6 | bBSA | 200 µg/ml |
note: bBSA on spot 5 was incubated for only a minute and then replaced with BSA
2015.09.03
Experiment/Protocol
Flush protocol:
Tet serum (-): 287 (1:10 diluted serum),429 (1:30 diluted serum)
Tet serum (+): 443 (1:10 diluted serum), 423 (1:30 diluted serum)
Reagent | Step | Flow rate (ul/min) | Priming time | Concentration |
---|---|---|---|---|
Buffer | 1 | 60 | 600 | 1x |
BSA | 2 | 60 | 600 | 10 mg/ml |
Buffer | 3 | 60 | 600 | 1x |
anti-GFP | 4 | 30 | 600 | 1.5 ug/ml |
Buffer | 5 | 60 | 300 | 1x |
Serum SIG002 (-)/(+) | 6 | 20 | 900 | 1:10 |
Buffer | 7 | 60 | 300 | 1x |
StrepCy5 | 8 | 30 | 600 | 5 ug/ml |
Buffer | 9 | 60 | 300 | 1x |
Results
Serum(-):
→ higher dilution of the blood serum leads to weaker iRif signal for mCherry, BSA,BSA+bBSA and bBSA but also for the tetanus antigen
Serum(+):
→ higher dilution of the blood serum leads to weaker iRif signal for mCherry, BSA,BSA+bBSA and bBSA but also for the tetanus antigen
→ signal of the tetanus antigen spot very weak compared to experiment 59a → use fresh stock of tetanus antigen next time
→ unspecific binding to the BSA spot is most of the time weaker than to mCherry → from now on BSA will be used as negative contol for blood serum
Experiment 64a: Salmonella antigen on PDITC slides for iRIf II
- protocols used :Plasma activation, iRIf slide preparation
2015.08.31
Experiment/Protocol
- 3 PDITC slides were prepared
- Plasma activation: 40 L/h, 5 min
- APTES incubation: 30 min
- PDITC incubation: 2 h
- desiccator: 15 min
- stored at 4 °C
2015.09.01
Experiment/Protocol
Spotting pattern:
# | spot | Concentration |
---|---|---|
1 | pos. control (GFP) | 0.5 mg/ml |
2 | bBSA | 0.5 mg/ml |
3 | Salmonella Antigen (15) | undiluted |
Slides (3): 208,215,216
2015.09.02
Experiment/Protocol
Flush protocol:
Reagent | Step | Flow rate (ul/min) | Priming time | Concentration |
---|---|---|---|---|
Buffer (TBS) | 1 | 60 | 600 | 1x |
BSA | 2 | 60 | 600 | 10 mg/ml |
Buffer (TBS) | 3 | 60 | 600 | 1x |
anti-GFP | 4 | 30 | 600 | 1,5 ug/ml |
Buffer (TBS) | 5 | 60 | 300 | 1x |
anti-Salmonella (13, desalt) | 6 | 30 | 900 | undiluted |
Buffer (TBS) | 7 | 60 | 300 | 1x |
StrepCy5 | 8 | 30 | 600 | 5 ug/ml |
Buffer (TBS) | 9 | 60 | 300 | 1x |
last slide (208) changed protocol: only 1 ug/ml anti-GFP used; anti-Salmonella desalt was mixed 1:1 with anti-Salmonella lysate
Results
Note: Slide 208 had the best signal.