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Team:Wageningen UR/Journal/week12
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| + | = week 12: 16 july - 20 july = | ||
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| + | == Office work == | ||
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== Lab work == | == Lab work == | ||
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the colonies transformed with the Hep B + BBa_PSB1K3.ml construct did not have any Hep B inserts | the colonies transformed with the Hep B + BBa_PSB1K3.ml construct did not have any Hep B inserts | ||
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| + | ---- | ||
| + | [[https://2012.igem.org/Team:Wageningen_UR/Journal/week11 previous week]] [[https://2012.igem.org/Team:Wageningen_UR/Journal/week13 next week]] | ||
Revision as of 16:34, 31 July 2012
week 12: 16 july - 20 july
Office work
Lab work
Bricking Hepatitis B
Tuesday:
- Digestion:
of the Hepatitis B PCR product (with pre- and suffix) with Spe1 and Pst1 of BBa_J04500 (an IPTG inducible promoter with RBS) with Xba1 and Pst1 of BBa_PSB1K3.ml (linearized plasmid backbone) with EcoR1 and Pst1
- PCR purification on the digest as a replacement for the heat inactivation
Wednesday:
- Ligation:
of the Hepatitis B PCR product with BBa_J04500 of the Hepatitis B product with BBa_PSB1K3.ml The ligations where done in duplo – once following the standard iGEM protocol and once using equimolar amounts of Hep B and the vector (DNA concentrations where measured by using NanoDrop)
- Electrotransformation in E.coli
- Grow transformed E.coli on plates containing kanamycin
A plasmid with a GFP coding device was used as a positive control (growing on a plate containing ampicillin)
Thursday:
- Colony PCR
of 20 colonies transformed with the Hep B + BBa_J04500 construct of 10 colonies transformed with the Hep B + BBa_PSB1K3.ml construct
Friday:
- gel electrophoresis (1% agarose gel) of the colony PCR samples
colony PCR of 20 colonies transformed with the Hep B + BBa_J04500:
the colonies transformed with the Hep B + BBa_PSB1K3.ml construct did not have any Hep B inserts
