Methods and compositions for pearl oyster cultivation

Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or... – Involving nucleic acid

Reexamination Certificate

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C435S252300, C435S325000, C536S023500

Reexamination Certificate

active

11049348

ABSTRACT:
The invention provides methods and compositions useful in pearl oyster cultivation. Polynucleotide and polypeptides relating to the nacre gene ofPinctada margaritiferaare provided. Antibodies related to these polypeptides, and compositions comprising polynucleotides, polypeptides and/or antibodies of the invention are also provided. The invention provides methods of using these polynucleotides, polypeptides and antibodies, including methods related to pearl oyster cultivation. Arrays comprising polynucleotides, polypeptides and/or antibodies of the invention are also provided.

REFERENCES:
patent: 4683195 (1987-07-01), Mullis et al.
patent: 4683202 (1987-07-01), Mullis
patent: 4736866 (1988-04-01), Leder et al.
patent: 4754065 (1988-06-01), Levenson et al.
patent: 4800159 (1989-01-01), Mullis et al.
patent: 4870009 (1989-09-01), Evans et al.
patent: 4873191 (1989-10-01), Wagner et al.
patent: 5124426 (1992-06-01), Primeaux, II et al.
patent: 5451514 (1995-09-01), Boudet et al.
patent: 5510270 (1996-04-01), Fodor et al.
patent: 5556752 (1996-09-01), Lockhart et al.
patent: 5578832 (1996-11-01), Trulson et al.
patent: 5723315 (1998-03-01), Jacobs et al.
patent: 5968772 (1999-10-01), Matsushiro
patent: 6001592 (1999-12-01), Nakashima et al.
patent: 6341580 (2002-01-01), Langdon
patent: WO-03/020019 (2003-03-01), None
patent: WO-03/020019 (2003-03-01), None
Genbank locus l14661 showing 38-nt fragment in the alignment of SEQ ID No. 1 with SEQ ID No.19 form USP 5451514.
Genbank locus AF061570 showing 37-nt fragment in alignment with instant SEQ ID No. 1.
Genbank locus AB032613, two sequences showing fragments greater than 25-nt.
Blanchard, A.P. et al. (1996). “High-Density Oligonucleotide Arrays,”Biosensors&Bioelectronics11(6/7):687-690.
DeRisi, J. et al. (1996). “Use of a cDNA Microarray to Analyse Gene Expression Patterns in Human Cancer,”Nature Genetics14:457-460.
Fodor, S. et al. (1991). “Light-Directed, Spatially Addressable Parallel Chemical Synthesis,”Science251:767-773.
GenBank Accession No. AB032613, created Dec. 27, 2005, located at <http://www.ncbi.nlm.nih.gov/entrez/viewer.fcgi?db=nuccore&val=6899835>, last visited on Mar. 15, 2006, two pages.
GenBank Accession No. AF061570, created May 9, 1998, located at <http://www.ncbi.nlm.nih.gov/entrez/viewer.fcgi?db=nuccore&val=3126867>, last visited on Mar. 15, 2006, two pages.
International Search Report mailed on Oct. 31, 2003, for PCT Application No. PCT/US02/23512 filed Jul. 23, 2002, 7 pages.
Khrapko, K.R. et al. (1991). “A Method for DNA Sequencing by Hybridization with Oligonucleotide Matrix,”DNA Sequence-J. DNA Sequencing and Mapping1:375-388.
Komachi, K. et al. (1994). “The WD Repeats of Tup1 Interact with the Homeo Domain Protein α2,”Genes&Development8:2857-2867.
Kono, M. et al. (2000). “Molecular Mechanism of the Nacreous Layer Formation inPinctada maxima,” Biochemical and Biophysical Research Communications269(1):213-218.
Lockhart, D.J. et al. (1996). “Expression Monitoring by Hybridization to High-Density Oligonucleotide Arrays,”Nature Biotechnology14:1675-1680.
Marshall, A. and Hodgson, J. (1998). “DNA chips: An Array of Possibilities,”Nature Biotechnoogy16:27-31.
Maskos,U. and Southern, E.M. (1992). “Oligonucleotide Hybridisations on Glass Supports: a Novel Linker for Oligonucleotide Synthesis and Hybridisation Properties of Oligonucleotides Synthesisedin situ,” Nucleic Acids Research20(7):1679-1684.
Matson, R.S. et al. (1995) “Biopolymer Synthesis on Polypropylene Supports: Oligonucleotide Arrays,”Analytical Biochemistry224(1):110-116.
Merrifield, R.B. (1963). “Solid Phase Peptide Synthesis. I. The Synthesis of a Tetrapeptide,”J. Am. Chem. Soc.85:2149-2154.
Pease, A.C. et al. (1994). “Light-Generated Oligonucleotide Arrays for Rapid DNA Sequence Analysis,”Proc. Natl. Acad. Sci. USA91:5022-5026.
Posnett, D.N. et al. (1988). “A Novel Method for Producing Anti-Peptide Antibodies,”Journal of Bioogical Chemistry263(4):1719-1725.
Ramsay, G. (1998). “DNA Chips: State-of-the Art,”Nature Biotechnology16:40-44.
Schena, M. et al. (1995). “Quantitative Monitoring of Gene Expression Patterns with a Complementary DNA Microarray,”Science270:467-470.
Schena, M. et al. (1996). “Parallel Human Genome Analysis: Microarray-Based Expression Monitoring of 1000 Genes,”Proc. Natl. Acad. Sci. USA93:10614-10619.
Shalon, D. et al. (1996). “A DNA Microarray System for Analyzing Complex DNA Samples Using Two-Color Fluorescent Probe Hybridization,”Genome Research6:639-645.
Smith, T.F. and Waterman, M.S. (1981). “Comparison of Biosequences,”Advances in Applied Mathematics2:482-489.
Spira, G. et al.(1984). “The Identification of Monoclonal Class Switch Variants by Sib Selection and an ELISA Assay,”Journal of Immunological Methods74:307-315.
Steplewski, Z. et al. (1985). “Isolation and Characterization of Anti-Monosialoganglioside Monoclonal Antibody 19-9 Class-Switch Variants,”Proc. Natl. Acad. Sci. USA82:8653-8657.
Tam, J.P. (1989). “High-Density Multiple Antigen-Peptide System for Preparation of Antipeptide Antibodies,”Methods of Enymology168:7-15.

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