You isolate nuclei from three different eukaryotic species. You
treat the samples in exactly the same way (adding same amount of
enzyme, buffer and time) to partially digest the chromatin with
micrococcal nuclease, extract the DNA, and run it on a gel. You see
the pattern below:
Lane
Approximate size of bands (in base pairs)
1
200, 400, 600, 800
2
180, 360, 540, 720
3
190, 380, 570, 760
a-2pts) Knowing that the core-DNA in all cell types is...