Team:Aachen/Notebook/Wetlab/May
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<a class="menulink" href="https://2014.igem.org/Team:Aachen/Notebook/Wetlab/March" style="color:black"> | <a class="menulink" href="https://2014.igem.org/Team:Aachen/Notebook/Wetlab/March" style="color:black"> | ||
<div class="menusmall-item menusmall-info" style="height:100px; width: 100px;" ><div class="menukachel" style="top: 30%; font-size: 16px;">Go to March</div></div> | <div class="menusmall-item menusmall-info" style="height:100px; width: 100px;" ><div class="menukachel" style="top: 30%; font-size: 16px;">Go to March</div></div> | ||
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== 8th == | == 8th == | ||
* The efficiency of our competent cells was tested | * The efficiency of our competent cells was tested | ||
- | *: → BL21: 6.6 x 10<sup>4</sup> | + | *: → BL21: 6.6 x 10<sup>4</sup> clones/µg DNA |
- | *: → DH5α: 2.59 x 10<sup>7</sup> | + | *: → DH5α: 2.59 x 10<sup>7</sup> clones/µg DNA |
* SOE-PCR step 2 like on 30.04. with the template of SOE1 from 30.04. was re-done | * SOE-PCR step 2 like on 30.04. with the template of SOE1 from 30.04. was re-done | ||
* The SOE2 product was run on a gel for checking (5 µL) | * The SOE2 product was run on a gel for checking (5 µL) | ||
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== 14th == | == 14th == | ||
* LB agar plates with chloramphenicol and some with ampicillin were made | * LB agar plates with chloramphenicol and some with ampicillin were made | ||
- | * REACh2 was purified on 1.2 | + | * REACh2 was purified on 1.2% agarose gel |
* A subsequent purification of the 778 bp fragment with High Pure PCR Product Purification Kit was done | * A subsequent purification of the 778 bp fragment with High Pure PCR Product Purification Kit was done | ||
== 19th == | == 19th == | ||
- | * K131026 was transformed into DH5α and NEB | + | * K131026 (AHL inducible GFP) was transformed into DH5α and NEB |
- | * K731520 was transformed into DH5α | + | * K731520 (IPTG inducible GFPmut3b) was transformed into DH5α |
== 20th == | == 20th == | ||
- | * Master plates | + | * Master plates with chloramphenicol (cam) → at least 6 clones on each plate |
* 2x 5 mL LB + cam were prepared | * 2x 5 mL LB + cam were prepared | ||
- | * Sterile 50 | + | * Sterile 50% glycerol was made |
== 21th == | == 21th == | ||
* Cryo stocks of clones 1 & 2 of each BioBrick/ host were prepared | * Cryo stocks of clones 1 & 2 of each BioBrick/ host were prepared | ||
* 15 mL cultures in 250 mL flasks, inoculated with 1.5 mL preculture (3 cultures A B C from clones 1; 1 + 2; 2) | * 15 mL cultures in 250 mL flasks, inoculated with 1.5 mL preculture (3 cultures A B C from clones 1; 1 + 2; 2) | ||
- | * 250 µl | + | * 250 µl cam from a 35 mg/mL stock was added |
* The cultures were grown until OD<sub>600</sub>= 0.6, then one was induced with IPTG | * The cultures were grown until OD<sub>600</sub>= 0.6, then one was induced with IPTG | ||
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<ul class="menusmall-grid"> | <ul class="menusmall-grid"> | ||
- | + | <!-- <li style="width:106px;margin-left: 12px;margin-right: 12px;" > | |
<a class="menulink" href="https://2014.igem.org/Team:Aachen/Notebook/Wetlab/March" style="color:black"> | <a class="menulink" href="https://2014.igem.org/Team:Aachen/Notebook/Wetlab/March" style="color:black"> | ||
<div class="menusmall-item menusmall-info" style="height:100px; width: 100px;" ><div class="menukachel" style="top: 30%; font-size: 16px;">Go to March</div></div> | <div class="menusmall-item menusmall-info" style="height:100px; width: 100px;" ><div class="menukachel" style="top: 30%; font-size: 16px;">Go to March</div></div> | ||
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Latest revision as of 16:11, 17 October 2014
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