From 2010.igem.org
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- | ''Notes:'' four tubes were marked and weighed (all had a mass of 1g). Bands were cut out of gels fron the | + | ''Notes:'' four tubes were marked and weighed (all had a mass of 1g). Bands were cut out of gels from |
| + | [[https://2010.igem.org/Team:SDU-Denmark/labnotes3#Restriction_and_Gel_extraction above]] |
Revision as of 13:09, 26 July 2010
Lab notes (7/26 - 7/30)
Group: Flagella
Incertion of Promoter + RBS in pSB3T5
Done by: Christian and Louise
Parts used: J13002 (promoter+RBS) and pSB3T5
Restriction and Gel extraction
Protocol: [RD1.1]
Notes: We made 2 Restriction mixtures which both were 4 times the mixture in the protocol. We also added 10 ul less water and 10 ul more PCR product than discribed in the protocol
Restriction mixture
- 38 ul Water
- 4 ul EcoRI enzyme
- 4 ul PstI enzyme
- 8 ul Fast Digest green buffer
- 30 ul PCR product (Freeze tube white 25 PROMOTER + RBS)
OR
- 30 ul PCR product (Freeze tube white 29 PLASMID)
Loading:
2 x 21 ul J13002 was loaded on a 2% gel with a 100-1000bp ladder. The Restricted J13002 is 95bp.
2 x 21 ul pSB3T5 was loaded on a 1.5% gel with a 100-10,000 ladder. The restristricted plasmid is 3215bp.
Result:
The picture shows a band around 100bp.
The picture showes two bands, one around 3000bp which is the plasmid and one around 1000bp, which is RFP.
Purification of J13002 and pSB3T5
Protocol:
Notes: four tubes were marked and weighed (all had a mass of 1g). Bands were cut out of gels from
[
above]