$62.14

Includes detailed instructions, chicken erythrocytes, prestained standard proteins, protein sample buffer, DNA sample buffer, calf thymus nucleosome standard DNA, nuclear isolation buffer, micrococcal nuclease, nuclear stain, EDTA, small transfer pipets and large transfer pipets.

Description

The primary level of chromosome structure in eukaryotes occurs when the DNA molecule is wrapped around histone proteins into particles called nucleosomes. Evidence for this “beads on a string” model is derived from nuclease digestion studies. When nuclei are incubated with micrococcal nuclease, the enzyme cleaves the linker DNA between nucleosomes (the string) but not the nucleosomal core DNA (the beads). With this background information, students isolate nuclei from chicken erythrocytes and then prepare nucleosomes from the nuclei by using a simple procedure that employs micrococcal nuclease. They then analyze the resulting nucleosome DNA fragments by agarose gel electrophoresis. They also determine the molecular weights of the five histone proteins associated with the isolated nucleosomes by comparing their migration on SDS-polyacrylamide gels to the migration of prestained standard proteins of known size. Sufficient chemicals are provided so that this experiment can be performed twice by 8 groups of students.

Requirements

This exercise requires a microcentrifuge, electrophoresis buffers, stains, agarose and three 12 well polyacrylamide gels for 8 groups of students.

Precast 12-well polyacrylamide gels can be purchased separately by calling Bio-Rad (800-424-6723) Their catalog number is 1611177.