Team:Aachen/Notebook/Wetlab/May
From 2014.igem.org
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(→May) |
(→May) |
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= May = | = May = | ||
== 1st == | == 1st == | ||
- | * gel with M - full -full - REACh1 SOE3.2 - REACH2 SOE3.2 - M | + | * A gel with M - full -full - REACh1 SOE3.2 - REACH2 SOE3.2 - M was run |
*: → 120 V, 30 min | *: → 120 V, 30 min | ||
*: → cut out the bands | *: → cut out the bands | ||
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== 5th == | == 5th == | ||
- | * | + | * Chemical competent DH5α and BL21 cells were made |
== 8th == | == 8th == | ||
- | * 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> | ||
*: → DH5α: 2.59 x 10<sup>7</sup> | *: → DH5α: 2.59 x 10<sup>7</sup> | ||
* 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 | ||
- | * SOE2 product was run on a gel for checking (5 µL) | + | * The SOE2 product was run on a gel for checking (5 µL) |
*: → restriction, (dephosphorylation of vector) | *: → restriction, (dephosphorylation of vector) | ||
*: → purification on a gel with high pure kit | *: → purification on a gel with high pure kit | ||
== 14th == | == 14th == | ||
- | * | + | * LB agar plates with chloramphenicol and some with ampicillin were made |
- | * REACh2 | + | * REACh2 was purified on 1.2 % agarose gel |
- | * subsequent purification of the 778 bp fragment with High Pure PCR Product Purification Kit | + | * 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 |
- | * | + | * K731520 was transformed into DH5α |
== 20th == | == 20th == | ||
- | * | + | * Master plates on chloramphenicol (cam) → at least 6 clones on each plate |
* prepared 2x 5 mL LB + cam | * prepared 2x 5 mL LB + cam | ||
* made sterile 50 % glycerol | * made sterile 50 % glycerol |
Revision as of 14:07, 13 October 2014
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