The eggs used in
this week’s protocols had an expiration date of 04/01/17. Per my mentor, to check if the eggs were
still usable a simple test was performed.
A raw egg was gently dropped into a beaker of water to see if it would
float (it didn’t float). If it did float
it meant the egg was no longer usable and if it stayed at the bottom of the
beaker it was usable. Also, another egg from the same carton was boiled and
gently dropped in a beaker full of water and it did not float. The eggs used
were carefully examined when cracked open to check for any discoloration or bad
smells both eggs used in the protocols appeared usable. Due to last week’s observations the
Ready-Lyse-Lysozyme used in the commercial kit was increased to a higher
concentration to adjust the DNA yields.
This was done because the DNA yields from the commercial kit were lower
than expected. After completing the
protocols from start to finish and running the samples (Egg White, Kit, and
Water Lysozyme) in the Nano drop machine the DNA yield numbers from the
commercial kit increased. Also each centrifuge tube was flicked/tapped to mix
contents, the volume of each centrifuge was relatively equal and the Providencia
stuartii TSB incubation period was increased to 48 hours. Next week the samples collected will be put
through gel electrophoresis and polymerase chain reaction. I’m excited to learn some new procedures and hopefully
the data collected from these tests will be more consistent.
Hey Mary, did you know about it before you performed this little trick? I have never heard of it! Now I know how to test whether an egg is good or not. Anyway, why did you increase the amount of time your bacteria was incubated? Did you not have enough? Hopefully everything is working out according to plan :)
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