Team:SDU-Denmark/labwork/Protocols/3A
From 2012.igem.org
(Difference between revisions)
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<td><a href="https://2012.igem.org/Team:SDU-Denmark/labwork/Protocols/revtrans">Reverse Transcriptase</a></td> | <td><a href="https://2012.igem.org/Team:SDU-Denmark/labwork/Protocols/revtrans">Reverse Transcriptase</a></td> | ||
- | <td><a href="https://2012.igem.org/Team:SDU-Denmark/labwork/Protocols/mutagen"> | + | <td><a href="https://2012.igem.org/Team:SDU-Denmark/labwork/Protocols/mutagen">Mutagenesis</a></td> |
<td><a href="https://2012.igem.org/Team:SDU-Denmark/labwork/Protocols/pcrgelclean">PCR-,gel clean-up</a></td> | <td><a href="https://2012.igem.org/Team:SDU-Denmark/labwork/Protocols/pcrgelclean">PCR-,gel clean-up</a></td> | ||
Latest revision as of 21:09, 26 September 2012
mRNA Isolation | PCR | Miniprep | Check Digest |
3A-Assembly | Colony-PCR | Transformation | Gel-electrophoresis |
Reverse Transcriptase | Mutagenesis | PCR-,gel clean-up |
3A-Assembly
- PCR step; see PCR protocol
- Digestion BSA is only needed for conventional restriction enzymes, NOT fast digest
- Digest step for Plasmid Backbone if sample comes from miniprep Enzyme Master Mix for Plasmid Backbone (25ul total)
- 5 ul Fastdigest greenbuffer / NEB Buffer 2
- 0.5 ul BSA
- 0.5 ul EcoRI-H
- 0.5 ul PstI
- 19 ul dH20 (0,5 ul less when using BSA)
- 5 ul Fastdigest greenbuffer / NEB Buffer
- 0.5 ul BSA
- 0.5 ul EcoRI-HF
- 0.5 ul PstI
- 0.5 ul DpnI (Used to digest any template DNA from productio
- 19 ul dH20 (0,5 ul less when using BSA
- Add 4 ul linearized plasmid backbone (25ng/ul for 100ng tota
- Add 4 ul of Enzyme Master Mix
- Digest 37C/30 min, heat kill Restriction Enzyme 80C/20 min
- Digest step for Insert X: If sample comes from miniprep Enzyme Master Mix for Plasmid Backbone (25ul total)
- 5 ul Fastdigest greenbuffer / NEB Buffer
- 0.5 ul BSA
- 0.5 ul EcoRI-HF
- 0.5 ul PstI
- 19 ul dH20 (0,5 ul less when using BSA
- 5 ul Fastdigest greenbuffer / NEB Buffer
- 0.5 ul BSA
- 0.5 ul EcoRI-HF
- 0.5 ul SpeI
- 0.5 ul DpnI (Used to digest any template DNA from production)
- 19 ul dH20 (0,5 ul less when using BSA)
- Add 4 ul linearized plasmid backbone (25ng/ul for 100ng total)
- Add 4 ul of Enzyme Master Mix
- Digest 37C/30 min, heat kill Restriction Enzyme 80C/20 min
- Digest step for Insert Y: If sample comes from miniprep Enzyme Master Mix for Plasmid Backbone (25ul total)
- 5 ul Fastdigest greenbuffer / NEB Buffer 2
- 0.5 ul BSA
- 0.5 ul EcoRI-HF
- 0.5 ul PstI
- 19 ul dH20 (0,5 ul less when using BSA)
- 5 ul Fastdigest greenbuffer / NEB Buffer 2
- 0.5 ul BSA
- 0.5 ul Xbal
- 0.5 ul PstI
- 0.5 ul DpnI (Used to digest any template DNA from production)
- 19 ul dH20 (0,5 ul less when using BSA)
- Add 4 ul linearized plasmid backbone (25ng/ul for 100ng total)
- Add 4 ul of Enzyme Master Mix
- Digest 37C/30 min, heat kill Restriction Enzyme 80C/20 min
- Ligation step
- Add 2ul of digested plasmid backbone (25 ng)
- Add 5:1 (Molar, NOT VOLUME)amount of EcoRI-HF SpeI digested fragment (Insert X)(< 3 ul)
- Add 5:1 (Molar, NOT VOLUME) amount of XbaI PstI digested fragment (Insert Y)(< 3 ul)
- Add 2 ul T4 DNA ligase buffer
- Add 0.5 ul T4 DNA ligase
- Add water to 10 ul
- Ligate 16C/30 min, heat kill 80C/20 min 3A Assembly. The part B0034 and C0010 is referred to as X and Y