US2003109002A1PendingUtilityA1
SIRP proteins and uses thereof
Assignee: MAX PLANCK GES ZUR FODERUNG DEPriority: Nov 15, 1996Filed: Nov 8, 2002Published: Jun 12, 2003
Est. expiryNov 15, 2016(expired)· nominal 20-yr term from priority
Y02A50/30C07K 16/18C07K 14/4703C12N 9/1205C07K 16/40A61K 38/00C12N 9/16
39
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Claims
Abstract
The present invention features isolated, purified, or enriched nucleic acid encoding a SIRP polypeptide and isolated, purified, or enriched SIRP polypeptide and uses thereof.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . An isolated, purified, or enriched nucleic acid encoding a SIRP polypeptide.
2 . The nucleic acid of claim 1 , wherein said SIRP polypeptide is a mammalian SIRP polypeptide.
3 . The nucleic acid of claim 2 , wherein said mammalian SIRP polypeptide is a human SIRP polypeptide.
4 . A nucleic acid probe for the detection of nucleic acid encoding a SIRP polypeptide in a sample.
5 . Recombinant nucleic acid encoding a SIRP polypeptide and a vector or a promoter effective to initiate transcription in a host cell.
6 . An isolated, purified, recombinant, or enriched SIRP polypeptide.
7 . The SIRP polypeptide of claim 5 , wherein said SIRP polypeptide is a mammalian SIRP polypeptide.
8 . The SIRP polypeptide of claim 6 , wherein said SIRP polypeptide is a human SIRP polypeptide.
9 . A purified antibody having specific binding affinity to a SIRP polypeptide.
10 . A hybridoma which produces an antibody having specific binding affinity to a SIRP polypeptide.
11 . A method of detecting a compound capable of binding to a SIRP polypeptide comprising the steps of incubating said compound with said SIRP polypeptide and detecting the presence of said compound bound to said SIRP polypeptide.
12 . A method of screening potential agents useful for treatment of a disease or condition characterized by an abnormality in a signal transduction pathway, wherein said signal transduction pathway includes an interaction between a SIRP polypeptide and a natural binding partner, comprising the step of assaying said potential agents for those able to promote or disrupt said interaction as an indication of a useful said agent.
13 . A method for diagnosis of a disease or condition characterized by an abnormality in a signal transduction pathway, wherein said signal transduction pathway includes an interaction between a SIRP polypeptide and a natural binding partner, comprising the step of detecting the level of said interaction as an indication of said disease or condition.
14 . A method for treatment of an organism having a disease or condition characterized by an abnormality in a signal transduction pathway, wherein said signal transduction pathway includes an interaction between a SIRP polypeptide and a natural binding partner comprising the step of promoting or disrupting said interaction.
15 . An isolated nucleic acid molecule comprising a nucleotide sequence that;
(a) encodes a polypeptide having the full length amino acid sequence set forth in SEQ ID NO.: 5, SEQ ID NO: 6, SEQ ID NO: 7, or SEQ ID NO: 8; (b) the complement of the nucleotide sequence of (a) or; (c) hybridizes under highly stringent conditions to the nucleotide sequence of (a) and encodes a naturally occurring SIRP protein.
16 . A nucleic acid molecule comprising a nucleotide sequence that encodes
(a) a SIRP protein having the full length amino acid sequence of sequence set forth in SEQ ID NO.: 5, SEQ ID NO: 6, SEQ ID NO: 7, or SEQ ID NO: 8 except that it lacks one of the following segments of amino acid residues: extracellular domain, transmembrane domain, cytoplasmic domain, tyrosine bearing SH2 binding region in the cytoplasmic domain; or (b) the complement of the nucleotide sequence of (a).
17 . An isolated nucleic acid molecule comprising a nucleotide sequence that encodes a polypeptide having the full length amino acid sequence set forth in SEQ ID NO: 5; SEQ ID NO: 6, SEQ ID NO: 7, or SEQ ID NO: 8 except that it lacks at least one, but not more than two, of the domains selected from the group consisting of the extracellular domain, the transmembrane domain, and the SHP-2 binding domain.
18 . A recombinant vector containing the nucleotide sequence of any one of claims 14 - 17 .
19 . A genetically engineered host cell containing the nucleotide sequence of any one of claims 14 - 18 .Join the waitlist — get patent alerts
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