Team:LMU-Munich/Cut'N'survive/Schedule

From 2010.igem.org

(Difference between revisions)
(Aim 1: DNA replication+PCR)
(Aim 2: Inserting PCR Products in pSB1C3 and verifying Sequenz)
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expected product size: 1233 bp
expected product size: 1233 bp
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==Aim 2: Inserting PCR Products in pSB1C3 and verifying Sequenz ==
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==Aim 2: Inserting PCR Products in pSB1C3 and verifying Sequence ==
PCR1: Insertion [ ] -> [[Team:LMU-Munich/Jump-or-die/Schedule/SequenzPCR1| Sequence of PCR1 from sequencing]]: confirmed [ ]
PCR1: Insertion [ ] -> [[Team:LMU-Munich/Jump-or-die/Schedule/SequenzPCR1| Sequence of PCR1 from sequencing]]: confirmed [ ]
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PCR3: Insertion [ ] -> [[Team:LMU-Munich/Jump-or-die/Schedule/SequenzPCR3| Sequence of PCR3 from sequencing]]: confirmed [ ]
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PCR3: Insertion [X] -> [[Team:LMU-Munich/Jump-or-die/Schedule/SequenzPCR3| Sequence of PCR3 from sequencing]]: confirmed [X]
PCR5: Insertion [ ] -> [[Team:LMU-Munich/Jump-or-die/Schedule/SequenzPCR5| Sequence of PCR5 from sequencing]]: confirmed [ ]
PCR5: Insertion [ ] -> [[Team:LMU-Munich/Jump-or-die/Schedule/SequenzPCR5| Sequence of PCR5 from sequencing]]: confirmed [ ]
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PCR6: Insertion [ ] -> [[Team:LMU-Munich/Jump-or-die/Schedule/SequenzPCR6| Sequence of PCR6 from sequencing]]: confirmed [ ]
PCR6: Insertion [ ] -> [[Team:LMU-Munich/Jump-or-die/Schedule/SequenzPCR6| Sequence of PCR6 from sequencing]]: confirmed [ ]
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PCR8: Insertion [ ] -> [[Team:LMU-Munich/Jump-or-die/Schedule/SequenzPCR8| Sequence of PCR8 from sequencing]]: confirmed [ ]
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PCR8: Insertion [X] -> [[Team:LMU-Munich/Jump-or-die/Schedule/SequenzPCR8| Sequence of PCR8 from sequencing]]: confirmed [X]
==Aim 3: Assembling Biobricks==
==Aim 3: Assembling Biobricks==

Revision as of 16:46, 24 October 2010



Contents

Aim 1: DNA replication+PCR

For PCR key see PCR key

Colourcode for the primers: Annealing part, mutagenised part, other sequences integrated into primer


PCR1: replication of the Tet-inducible CMV promotor [X] PCR1.jpg

Primer used: 1TreF 2TreR expected product size: 492bp


PCR2a: replication of the TEVrecogn-NDegron-SF3 Part with mutagenisis (EcoR1 + Pst1) [X] PCR2a.jpg

Primer used: 3TevF 4TevMutEPR expected product size: 332 bp


PCR2b: replication of the TEVrecogn-NDegron-SF3 Part with mutagenisis (EcoR1 + Pst1) [X] PCR2b.jpg

Primer used: 5TevMutEPF 6TevR expected product size: 772 bp


PCR3: joining PCR of the TEVrecogn-NDegron-SF3 Part [X] PCR3.jpg

Primer used: 3TevF 6TevR expected product size: 1087 bp


PCR4a: replication human bak with mutagenisis (Pst1) [X] PCR4a.jpg

Primer used: 7BakF 8BakMutPR expected product size: 330 bp


PCR4b: replication human bak with mutagenisis (Pst1) [X] PCR4b.jpg

Primer used: 9BakMutPF 10BakR expected product size: 376 bp


PCR5: joining PCR of human bak [X] PCR5.jpg

Primer used: 7BakF 10BakR expected product size: 688 bp


PCR6: replication of the SV40-polyadenylation site [X] PCR6.jpg

Primer used: 11PAF 12PAR expected product size: 237 bp


PCR7a: replication of the p14*TEVrecogn with mutagenisis (Spe1) [X] PCR7a.jpg

Primer used: 13TrecF 14TrecMutSR expected product size: 850 bp


PCR7b: replication of the p14*TEVrecogn with mutagenisis (Spe1) with TEV recogn in primer (16TrecR) [X] PCR7b.jpg

Primer used: 15TrecMutSF 16TrecR expected product size: 402 bp


PCR8: joining PCR of p14*TEVrecogn with TEV recogn in primer (16TrecR) [X] PCR8.jpg

Primer used: 13TrecF 16TrecR expected product size: 1233 bp

Aim 2: Inserting PCR Products in pSB1C3 and verifying Sequence

PCR1: Insertion [ ] -> Sequence of PCR1 from sequencing: confirmed [ ]

PCR3: Insertion [X] -> Sequence of PCR3 from sequencing: confirmed [X]

PCR5: Insertion [ ] -> Sequence of PCR5 from sequencing: confirmed [ ]

PCR6: Insertion [ ] -> Sequence of PCR6 from sequencing: confirmed [ ]

PCR8: Insertion [X] -> Sequence of PCR8 from sequencing: confirmed [X]

Aim 3: Assembling Biobricks

We are using the 3A System to assemble Biobricks.

Assembling Construct 1

N1S.jpg

Assembling Construct 2

N2S.jpg

Aim 4: Testing products

Construct 1

TEV Construct 1: Inserted in celline

- transform into HeLa cells to see if they survive.

-> Check the leakiness of tet-on-promoter

- induce tet-on-promoter to see, if cells die.

-> Check if construct 1 is working

Construct 2

TEV Construct 2: Contains gene of interest

- Transform into HeLa cells and see if eGFP is being translated

-> Check if CMV-promoter is working and construct is being read-off completely

- Western Blot

-> Check by reference of protein size if eGFP is cut off from the residual of the protein by TEV-Protease

Aim 5: Testing system