(Downloading may take up to 30 seconds.
If the slide opens in your browser, select File -> Save As to save it.)
Click on image to view larger version.

Fig. 6. Chromatin condensation and nuclear re-organisation of Hoxb in the
E6.5 early streak embryo. (A) HE staining (left) and DAPI counterstaining
(right) of serial transverse sections from an E6.5 embryo. The position of the
posterior streak region (PSR), and the posterior (PEP) and anterior (AEP)
epiblast are indicated. Scale bar: 200 µm. (B) The distribution of squared
interphase distances (d2) measured between probes for
Hoxb1 and Hoxb9, in PSR, DR, PEP and AEP of E6.5 embryos.
Measurements from E7.5 EEM are shown for comparison. (C) Histogram showing the
position of Hoxb1 hybridisation signals, relative to the MMU11
territory edge, in nuclei from E7.5 EE (black bars), E6.5 DR (white bars) and
E6.5 PSR (grey bars). Negative distances indicate signals localised beyond the
visible limits of the detectable CT (n
60). (D) Position
(mean±s.e.m.) of Hoxb1 (squares) and Hoxb9 (circles)
relative to the MMU11 territory edge in nuclei from E7.5 EE and E6.5 PSR
(n
60).