This week for
the pseudomonas project we will be doing gel electrophoresis on our samples. We
have done water and biofilm collection. We moved on to do filtration, using a filtration
apparatus we trapped any bacteria onto a filter. That filter was then
transferred onto a plate to allow for us to culture the bacteria. The growth
was then transferred into broth to allow to proceed into DNA extraction. For
the DNA extraction we follow a protocol. I found this protocol interesting
because we can see the chromosomal DNA threads being formed. We moved on to Nano
drop to see the DNA concentration. Once we finished Nano dropping we moved on
to PCR. What PCR does is amplifies our DNA using primers that are specific to
the pseudomonas we are looking for. Next week we hope to have our gel
electrophoresis results and maybe move on to DNA sequencing.
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