US2012270809A1PendingUtilityA1

Human transmembrane proteins

48
Assignee: TANG Y TOMPriority: May 29, 1998Filed: May 22, 2012Published: Oct 25, 2012
Est. expiryMay 29, 2018(expired)· nominal 20-yr term from priority
A61P 3/10A61P 9/10A61P 37/02A61P 5/24A61P 7/06A61P 7/02A61P 31/04A61P 25/14A61P 25/06A61P 25/28A61P 31/12A61P 25/16A61P 25/00A61P 33/00A61P 35/00A61P 31/10C07K 2317/76G01N 33/68A61P 11/06A61P 1/12A61P 1/08A61K 38/00A61P 1/16C07K 2317/24A61P 1/04A61P 15/10C07K 16/28A61P 1/10C07K 2317/622A61P 17/06A61P 15/08A61P 19/02C07K 14/705
48
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Claims

Abstract

The invention provides human transmembrane proteins (HTMPN) and polynucleotides which identify and encode HTMPN. The invention also provides expression vectors, host cells, antibodies, agonists, and antagonists. The invention also provides methods for diagnosing, treating, or preventing disorders associated with expression of HTMPN.

Claims

exact text as granted — not AI-modified
1 .- 20 . (canceled) 
     
     
         21 . An isolated polypeptide comprising an amino acid sequence having at least about 90% sequence identity to SEQ ID NO: 74. 
     
     
         22 . An isolated polypeptide comprising an amino acid sequence having at least about 95% sequence identity to SEQ ID NO: 74. 
     
     
         23 . The isolated polypeptide of  claim 21  comprising SEQ ID NO: 74. 
     
     
         24 . The isolated peptide of  claim 21  which has been modified by one or more of acetylation, carboxylation, glycosylation, phosphorylation, lipidation, or acylation. 
     
     
         25 . The isolated peptide of  claim 21  which is ligated to a heterologous amino acid sequence. 
     
     
         26 . A composition comprising the polypeptide of  claim 21  and at least one pharmaceutically acceptable excipient. 
     
     
         27 . A method of screening a compound for effectiveness as an agonist of the polypeptide of  claim 21 , the method comprising:
 (a) exposing a sample comprising the polypeptide of  claim 21  to the compound, and   (b) detecting agonist activity in the sample.   
     
     
         28 . A method of screening a compound for effectiveness as an antagonist of the polypeptide of  claim 21 , the method comprising:
 (a) exposing a sample comprising the polypeptide of  claim 21  to the compound, and   (b) detecting antagonist activity in the sample.   
     
     
         29 . A method of screening for a compound that specifically binds to the polypeptide of  claim 21 , the method comprising:
 (a) combining the polypeptide of  claim 21  with at least one test compound under suitable conditions, and   (b) detecting binding of the polypeptide of  claim 21  to the test compound, thereby identifying a compound that specifically binds to the polypeptide of  claim 21 .   
     
     
         30 . An antibody that specifically binds to a polypeptide comprising SEQ ID NO: 74. 
     
     
         31 . The antibody of  claim 28  which is labeled. 
     
     
         32 . The antibody of  claim 29 , wherein the label is selected from the group consisting of radionuclides, enzymes, fluorescent, chemiluminescent, and chromogenic agents. 
     
     
         33 . The antibody of  claim 30  which is monoclonal.

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