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Team:Freiburg/Content/Notebook/Labjournal
From 2014.igem.org
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<p class="desc">200 µl transfection mix per well (3 µg DNA, 7,5 µl PEI, rest OptiMEM), transfection control: pEGFP_C1</p> | <p class="desc">200 µl transfection mix per well (3 µg DNA, 7,5 µl PEI, rest OptiMEM), transfection control: pEGFP_C1</p> | ||
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| - | <p class="desc"> | + | <p class="desc">(left) Cho cells: without receptor were transduced with MuLV IRES EGFP ,(right) CHO cells transfected with SLC7a1 and transduced with MuLV IRES EGFP (24h after transfection)</p> |
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Revision as of 13:59, 3 October 2014
Cloning
Cloning - May
Cloning - June
Cloning - July
Cloning - August
Cloning - September
Cloning - October
Viral Vectors
Viral Vectors - May
2014/05/21
Transfection/ Virus production
For virus production Phoenix cells (producer cell line) were splitted (well separated) on 100mm plates. At 70% cell density cells were transfected using polyethylenimine.
- remove medium and refill with 5 ml new completed growth medium (DMEM)
- 600 µl transfection mastermix was prepared (8 µg pMIG IRES EGFP, 24 µl PEI, rest OptiMEM)
- mastermix was incubated 15 min and carefully drop on the plates
Plates were incubated at 37°C. The supernatant after 24 was removed and refilled with 5 ml new DMEM, the supernatant was collected after 48 h (refilled with 5 ml DMEM) as well as 72 h.
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Phoenix cells transfected with pMIG IRES EGFP one day after transfection.
2014/05/25
Transduction mouse cells
NIH 3T3 cells (60% density) were transduced with MuLV IRES EGFP.
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- 500 µl of supernatant was removed
- 1 µl Polybrene was added (10mg/ml)
- 500 µl virus supernatant was added (sterile filtered)
- incubation at 37°C for 6h
- cell supernatant was replaced with fresh DMEM
- transduction was repeated once
Pictures could be made after 48 h of incubation.
Anderes Foto
NIH 3T3 cells were transduced twice with MuLV IRES EGFP for 6h. Picture was made after 48 h of incubation at 37°C.
Viral Vectors - June
2014/06/20
Thawing of eukaryotic cells
New Phoenix cell stocks were thawed:
- cryotube was thawed at 37°C water bath until almost defrosted
- stock was filled in 9 ml warm DMEM and centrifuged at 900 rpm for 2 min
- medium was removed and refilled with 10 ml warm DMEM
- cells were seeded on 100 mm plate
Testing optimal cell density of mouse fibroblasts
NIH 3T3 have a really fast growth so that we tested the optimal cell number for seeding NIH 3T3 for having around 60% cell density on the next day. NIH 3T3 cells grow very fast; therefore we have tested the optimal seeding cell number to obtain 60% cell density on the next day.
NIH 3T3 cells were transduced twice with MuLV IRES EGFP for 6h. Picture was made after 48 h of incubation at 37°C (2014-05-28-nih-3t3-100mm-mulv-pmig-ires-egfp-transd-48h)
- incubation for 24 h at 37°C
--> optimal cell number is 1 – 1.5x10^5 cells per well ( = 0.5 – 0.75 cells/ml)
2014/06/22
Transfection/ Virus production
Transfection of Phoenix cells (70% density) with pMIG IRES EGFP (protocol: 2014/05/21) (2 x 100mm plate)
Anderes Foto
3 Phoenix cells transfected with pMIG IRES EGFP after 3d.
2014/06/24
Transfection/ Virus production
Transfection of Phoenix cells (70% density) with pMIG IRES EGFP (protocol: 2014/05/21) (5 x 100mm plate)
2014/06/27
Thawing new HEK 293 cells
(protocol: 2014/06/20)
Transfection CHO cells with receptor
Transfection of CHO cells with SLC7a1 (for later transduction with virus). Medium was changed after 5 h. Cells were incubated for 24 h before viral transduction with MuLV IRES EGFP, medium change after 16 h.
200 µl transfection mix per well (3 µg DNA, 7,5 µl PEI, rest OptiMEM), transfection control: pEGFP_C1
(left) Cho cells: without receptor were transduced with MuLV IRES EGFP ,(right) CHO cells transfected with SLC7a1 and transduced with MuLV IRES EGFP (24h after transfection)
