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Team:Evry/Interlab Study/09-11-2014
From 2014.igem.org
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<i>PSB1C3+E0240+J23101</i> and <i>PSB1C3+E0240+J23118</i>,<br> | <i>PSB1C3+E0240+J23101</i> and <i>PSB1C3+E0240+J23118</i>,<br> | ||
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| - | <li> PCR colony of | + | <li> PCR colony of 3 colonies for each construction following protocol table 1 and 2. |
https://static.igem.org/mediawiki/2014/c/c1/Gel11092014.jpg | https://static.igem.org/mediawiki/2014/c/c1/Gel11092014.jpg | ||
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<li> PCR purification of sample 1 and 4 of the Gel 1 were purified with the NucleoSpin kit (Macherey Nagel). DNA was quantify by Nanodrop 2000. | <li> PCR purification of sample 1 and 4 of the Gel 1 were purified with the NucleoSpin kit (Macherey Nagel). DNA was quantify by Nanodrop 2000. | ||
Revision as of 18:18, 19 September 2014
Construction n°1: PSB1C3 with I20260
Construction n°2: PSB1C3 with J23101-E1010
Construction n°3: PSB1C3 with K823012-E1010
Other constructions of the Anderson library of constitutive promoters
PSB1C3+E0240+J23101, PSB1C3+E0240+J23118, PSB1C3+E0240+J23105, PSB1C3+E0240+J23106 and PSB1C3+E0240+J23107:
- Transformation plate from the 10th September observation. There were 50 colonies for each constructions.
PSB1C3+E0240+J23101 and PSB1C3+E0240+J23118,
- PCR colony of 3 colonies for each construction following protocol table 1 and 2.
https://static.igem.org/mediawiki/2014/c/c1/Gel11092014.jpg
GEL 1: 1% agarose gel. Lane 1 to 3: PCR product of 3 colonies of the PSB1C3+E0240+J23101 construction. Lane 4 to 6: PCR product of 3 colonies of the PSB1C3+E0240+J23118 construction. - PCR purification of sample 1 and 4 of the Gel 1 were purified with the NucleoSpin kit (Macherey Nagel). DNA was quantify by Nanodrop 2000.
- Preparation of samples to sequencing. N° XX
- Preparation of 3 ml cultures LB Cam. Incubation overnight at 37°C.
Sep 11
