Nucleic acids encoding PRO189 polypeptides
AssigneeGenentech, Inc.
InventorsDavid Botstein, Audrey Goddard, Paul J. Godowski, Austin L. Gurney, Margaret Ann Roy, William I. Wood
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Abstract
The present invention is directed to novel polypeptides and to nucleic acid molecules encoding those polypeptides. Also provided herein are vectors and host cells comprising those nucleic acid sequences, chimeric polypeptide molecules comprising the polypeptides of the present invention fused to heterologous polypeptide sequences, antibodies which bind to the polypeptides of the present invention and to methods for producing the polypeptides of the present invention.
Claims12
An isolated nucleic acid comprising:
- (a) a nucleic acid sequence encoding the polypeptide of SEQ ID NO:
- 326;
- (b) a nucleic acid sequence encoding the polypeptide of SEQ ID NO:
- 326, lacking its associated signal peptide;
- (c) the nucleic acid sequence of SED ID NO:
- 325;
- (d) the full-length coding sequence of the cDNA deposited under ATCC accession number 203129;
- wherein, said nucleic acid is amplified in colon tumors.
An isolated nucleic acid molecule consisting of at least a 20 nucleotide fragment of the nucleic acid sequence of SEQ ID NO:
- 325 or a complement thereof that specifically hybridizes under stringent conditions to:
- (a) the nucleic acid sequence of SEQ ID NO:
- 325 or a complement thereof;
- or
- (b) the full-length coding sequence of the cDNA deposited under ATCC accession number 203129 or a complement thereof;
- wherein, said stringent conditions use 50% formamide, 5× SSC, 50 mM sodium phosphate (pH 6.8), 0.1% sodium pyrophosphate, 5× Denhardt's solution, sonicated salmon sperm DNA (50 μg/ml), 0.1% SDS, and 10% dextran sulfate at 42° C., and washes at 42° C. in 0.2× SSC, at 55° C. in 50% formamide followed by a high-stringency wash at 55° C. in 0.1× SSC, EDTA;
- and wherein said isolated nucleic acid molecule is suitable for use as a PCR primer or probe.
Dependencies are inferred from the claim text.