In cells, the genome needs to be tightly packaged in the nucleus as "chromatin" while still allowing access to the cellular machinery responsible for gene expression. The first level of packaging involves the "core histone” proteins, which form spools around which two turns of DNA are wrapped, a series of which gives rise to an array resembling "beads on a string". This is further condensed by "linker histone" proteins, one of which binds to each spool, arranging them into a thicker fibre. The precise way in which this is accomplished is, despite decades of research, still a hotly debated topic since linker histones have long tails that do not have a static defined 3D structure even when bound to the linker DNA that they are directly responsible for condensing, thus conventional diffraction-based methods fail. We aim to use SANS for this important piece of the chromatin structure puzzle.