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Kyunghwa Jeong edited Results_sleep.tex
almost 9 years ago
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\subsection*{DmCa\textsubscript{v}3 mutants show increased sleep}
Since the Gal4 coding sequence inserted into \emph{DmCa\textsubscript{v}3\textsuperscript{Founder}} to produce the \emph{DmCa\textsubscript{v}3\textsuperscript{Gal4}} allele included a termination sequence (Fig. \ref{fig:3}a), \emph{DmCa\textsubscript{v}3\textsuperscript{Gal4}} is likely a null allele.
As expected, we were unable to detect DmCa\textsubscript{v}3 expression in the fly head lysates
from \emph{DmCa\textsubscript{v}3\textsuperscript{Gal4}} flies in western blot analyses using polyclonal DmCa\textsubscript{v}3-specific antisera (Fig. \ref{fig:3}a). We did, however, detect strong DmCa\textsubscript{v}3 expression in fly lysates from \emph{w\textsuperscript{1118}} controls and from a \emph{DmCa\textsubscript{v}3\textsuperscript{Rescue}} allele in which the fragment deleted in both the \emph{DmCa\textsubscript{v}3\textsuperscript{Founder}} and \emph{DmCa\textsubscript{v}3\textsuperscript{Gal4}} alleles was re-inserted (Fig. \ref{fig:3}a and b).
\emph{DmCa\textsubscript{v}3\textsuperscript{Gal4}} homozygote flies were viable and fertile with normal appearance and no movement defect.
In mammals, two T-type channel subtypes of a1G and a1I involve in generation of neural oscillation in NREM sleep.
It is well established that flies have sleep-like state and share conserved mechanisms with mammals although it is still not clear whether flies have distinct sleep stages.
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