Team:Warsaw/Calendar-Main/6 May 2008
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<a name="fig1"><img src="https://static.igem.org/mediawiki/2008/3/3c/Genomic_DNA_WAW.jpg"/></a> | <a name="fig1"><img src="https://static.igem.org/mediawiki/2008/3/3c/Genomic_DNA_WAW.jpg"/></a> | ||
- | <var><b>Fig. 1.</b> Probes of isolated genomic DNA after mechanical destruction. 1 and 3-<i>E.coli</i> Rosetta DNA; 2-DNA ladder; 4-<i>E.coli</i> TOP10 DNA.</var> | + | <var><b>Fig. 1.</b> Probes of isolated genomic DNA after mechanical destruction by pipetting. Without destruction the DNA wouldn't be visible in this kind of gel because genomic DNA is too big. 1 and 3-<i>E.coli</i> Rosetta DNA; 2-DNA ladder; 4-<i>E.coli</i> TOP10 DNA.</var> |
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Revision as of 20:13, 12 October 2008
Preparation of pMPMT5+AID constructPiotr, Weronika
Isolation of genomic DNAMichał L.
Isolation of genomic DNA (E.coli Rosetta and TOP10) - template DNA for PCR to obtain T7 polymerase DNA. DNA isolated from E. coli TOP10 strain was used as a negative control for PCR. Fig. 1. |