A procedure is described that facilitates the isolation of large quantities of nuclei (germinal vesicles or GVs) from late stage Xenopus laevis oocytes. The method was developed by modifying techniques described in two published reports (F. Scalenghe et al. (1978) Chromosoma 66, 299-308; I. Ruberti et al. (1989) Anal. Biochem. 180, 177-180). Methods were chosen which optimize yields of GVs and homologous recombination activity. This procedure yields up to (90 %) of the total GVs present in (70 \mathrm{ml}) of oocytes. Proteins in the extract made from these GVs are predominantly of nuclear origin; little cytoplasmic contamination is detected as measured by (\alpha)-tubulin content. The extract catalyzes the complete recombination of linear, terminally homologous DNA, as observed in injected oocytes. The extract also performs other nuclear processes including transcription, repair-type DNA synthesis, chromatin assembly, NDP kinase reactions, and dsRNA deamination. Because this procedure greatly increases the yield of GVs over manual isolation protocols, and the resulting extract is capable of carrying out a variety of typical nuclear processes, it should expedite the purification of components found in oocyte GVs, including proteins required for homologous recombination. (c) 1993 Academic Press, Inc.