Appeal No. 2004-1967 Page 5 Application No. 09/027,439 hybridization at 40°-65°C for 14-16 hours in a hybridization solution at pH 7.8, containing 0.9 M NaCl, 0.12 M Tris-HCl, 6 nM EDTA, 0.1 M sodium phosphate buffer, 0.1% SDS and 0.1% polyvinylpyrrolidone, followed by three 15-minute washes at 40°-65°C to remove unbound probes in a solution at pH 7, containing 0.075 M NaCl, 0.0075 M Na Citrate and 0.1% SDS. 53. An isolated nucleic acid molecule comprising a nucleotide sequence of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, or SEQ ID NO: 6, or an RNA equivalent thereof, or a nucleic acid complementary to said isolated molecule, capable of base- pairing according to standard Watson-Crick complementarity rules. The claims stand rejected as follows: I. Claims 55-58 under 35 U.S.C. § 112, second paragraph, as indefinite. II. Claims 55-58 under 35 U.S.C. § 101 as “directed to non-statutory subject matter. III. Claims 47, 48, 53 and 55-58 under 35 U.S.C. § 102(a) and (e) as anticipated by Hogan.2 IV. Claims 47, 48, 53 and 55-58 under 35 U.S.C. § 102(a) as anticipated by Genbank Accession No. X969643 or X807264 (disclosed in Cilia5). V. Claims 47, 48, 53 and 55-58 under 35 U.S.C. § 103 as unpatentable over Genbank Accession No. A145656 and Dyson.7 2 Hogan et al., U.S. Patent 5,541,308, issued July 30, 1996. 3 Genbank Accession No. X96964, February 4, 1996. 4 Genbank Accession No. X80726, March 29, 1996. 5 Cilia et al., “Sequence Heterogeneities Among 16S Ribosomal RNA Sequences, and Their Effect on Phylogenetic Analyses at the Species Level,” Mol. Biol. Evol., Vol. 13, No. 3, pp. 451-461 (February 20, 1996). 6 Genbank Accession No. A14565, September 29, 1994. 7 Dyson, N.J., in Essential Molecular Biology Vol. II: A Practical Approach, Chapter 5, pp. 11-156, Brown, T.A. ed., Oxford University Press, 1992.Page: Previous 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 NextLast modified: November 3, 2007