Raj Magesh (Talk | contribs) |
Raj Magesh (Talk | contribs) |
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<h1 id="biobrick-transformations">BioBrick Transformations</h1> | <h1 id="biobrick-transformations">BioBrick Transformations</h1> | ||
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+ | <p>The five BioBricks we are using are transformed into <i>E. coli</i> strain DH5α — chosen for its <i>recA</i> and <i>endA</i> mutations that allow for high-yield minipreps.</p> | ||
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+ | <h2>INSERT IMAGES OF PLATES</h2> | ||
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<h1 id="plasmid-isolation">Plasmid Isolation</h1> | <h1 id="plasmid-isolation">Plasmid Isolation</h1> | ||
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+ | <p>Minipreps are performed from three colonies on each plate to confirm the presence of the plasmid. One colony from each positive transformants is used to make a glycerol stock.</p> | ||
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+ | <h2>INSERT GEL IMAGES</h2> | ||
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<h1 id="pcrs">PCRs: Adding Restriction Sites and Linkers</h1> | <h1 id="pcrs">PCRs: Adding Restriction Sites and Linkers</h1> | ||
+ | Our assembly begins with our PCRs: using carefully-designed primers with 5'-overhangs, we add restriction sites, linkers and other features to our parts of interest. | ||
+ | <h2>PCR 1: Piece 1 of the T7 Expression Backbone</h2> | ||
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+ | <table> | ||
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<h1 id="restriction-digests">Restriction Digests</h1> | <h1 id="restriction-digests">Restriction Digests</h1> | ||
<table> | <table> |
Revision as of 09:55, 31 October 2017
BioBrick Transformations
The five BioBricks we are using are transformed into E. coli strain DH5α — chosen for its recA and endA mutations that allow for high-yield minipreps.
INSERT IMAGES OF PLATES
Plasmid Isolation
Minipreps are performed from three colonies on each plate to confirm the presence of the plasmid. One colony from each positive transformants is used to make a glycerol stock.
INSERT GEL IMAGES
PCRs: Adding Restriction Sites and Linkers
Our assembly begins with our PCRs: using carefully-designed primers with 5'-overhangs, we add restriction sites, linkers and other features to our parts of interest.PCR 1: Piece 1 of the T7 Expression Backbone
Restriction enzymes used in our assembly | |||||||
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Restriction Enzyme | Sequence | Activity in NEBuffers (%) | Incubation temperature | Heat inactivation | |||
1.1 | 2.1 | 3.1 | CutSmart | ||||
AgeI | A\CCGGT | 100 | 75 | 25 | 75 | 37°C | 65°C |
AgeI-HF | A\CCGGT | 100 | 50 | 10 | 100 | 37°C | 65°C |
BamHI | G\GATCC | 75* | 100* | 100 | 100* | 37°C | — |
BamHI-HF | G\GATCC | 100 | 50 | 10 | 100 | 37°C | — |
HindIII | A\AGCTT | 25 | 100 | 50 | 50 | 37°C | 80°C |
HindIII-HF | A\AGCTT | 10 | 100 | 10 | 100 | 37°C | 80°C |
HindIII | A\AGCTT | 25 | 100 | 50 | 50 | 37°C | 80°C |
HindIII-HF | A\AGCTT | 10 | 100 | 10 | 100 | 37°C | 80°C |
NcoI | C\CATGG | 100 | 100 | 100 | 100 | 37°C | 80°C |
NcoI-HF | C\CATGG | 50 | 100 | 10 | 100 | 37°C | 80°C |
NheI | G\CTAGC | 100 | 100 | 10 | 100 | 37°C | 65°C |
NheI-HF | G\CTAGC | 100 | 25 | 10 | 100 | 37°C | 80°C |
* denotes star activity| NOTE ADD NdeI TOO |