From: Derek Gatherer (d.gatherer@vir.gla.ac.uk)
Date: Fri 02 Dec 2005 - 12:06:14 GMT
Apologies if this duplicates in your inbox. The previous version
didn't reach me, and some formatting problems have started to appear
in some messages.
Message was:
Exactly, the selection medium simply gets living cells dumped in on
top of the dead ones. The same flask is used, not a clean one. In the
unselected medium there is passage (which means spinning down cells,
taking an aliquot and seeding it into a clean flask with fresh
medium). So tell me then, where's the control? What is being compared
with what?
At 20:46 30/11/2005, Dace wrote:
>Derek,> From: Derek Gatherer
<<mailto:d.gatherer@vir.gla.ac.uk?Subject=Re:%20Miroslav%20Hill%20responds>d.gatherer@vir.gla.ac.uk>>>
Before you
>start fulminating, Ted, I suggest you re-read Hill's>
>paper. (bottom of p212 and the first paragraph of 213). Then
>reread> his reply.I don't see the contradiction. In response to
>your question, Dr. Hill saidthat at each passage the culture was
>divided into two subpopulations whichwere both placed in clean
>flasks. Here's what he wrote in his paper:"Briefly, cells in the
>logarithmic phase of growth are, at each passage,divided into two
>unequal samples and subcultured by seeding the large sampleinto a
>selection medium and by growing the small one in a parallel
>culturewithout selection."No contradiction there. Perhaps you were
>thinking of what he wrote next:"The cell monolayer in the selection
>medium, when depleted, is periodicallyreplenished by the addition of
>fresh cells from the parallel culture."This is a separate issue,
>having nothing to do with splitting the culture ateach
>passage. Since the exposed culture is depleted by the toxin, it has
>tobe replenished with cells from the unexposed culture. Are you
>suggestingthat this somehow contaminated the unexposed culture? You
>have yet toexplain how Dr. Hill's results were compromised.ted> At
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