Team:UAB-Barcelona/ext
From 2009.igem.org
Revision as of 03:16, 22 October 2009 by Antonio.freire (Talk | contribs)
We used in both cases Wizard Genomic DNA Purification Kit (PROTOCOL).
Extraction of N. europaea DNA
To verify that we had enough concentration of DNA to makethe PCR (approximately 100 ng of DNA) we measured the concentration and purity of the DNA (there is recommended that the ratio 260/280 should be major that 1.8) with the Nanodrop. Furthermore, we verified the integritied of the DNA by electrophoresis.
Quantification of Nitrosomonas genomic DNA by Nanodrop [DNA] (ng/microl) Relation Abs 260/280 74.1 1.92 104.2 1.92 241.0 1.95 284.6 1.87
Agarose gel to verify the integrity of the Nitrosomonas europea genomic DNA.
From left side to right: Gene ruler DNA Ladder; Nitrosomonas europea genomic DNA.
Extraction of E.coli DNA
Quantification of E. coli genomic DNA by Nanodrop [DNA] (ng/microl) Relation Abs 260/280 885 2.16 1507 2.05
Agarose gel to verify the integrity of the E. coli genomic DNA.