US2009305232A1PendingUtilityA1

Peptides for Detection of Antibody to Porcine Reproductive Respiratory Syndrome Virus

Assignee: IDEXX LABORATOIRES INCPriority: Feb 25, 2005Filed: Jul 7, 2009Published: Dec 10, 2009
Est. expiryFeb 25, 2025(expired)· nominal 20-yr term from priority
C12N 2770/10022C07K 14/005G01N 33/56983C07K 16/10G01N 2469/10C07K 2319/21G01N 2469/20
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Claims

Abstract

The invention provides compositions and methods for the detection and quantification of PRRSV antibodies and antibody fragments using polypeptides.

Claims

exact text as granted — not AI-modified
1 . A method of detecting a porcine reproductive and respiratory syndrome virus (PRRSV) polypeptide or PRRSV in a sample comprising:
 (a) contacting one or more antibodies that specifically bind to at least one epitope of an PRRSV polypeptide, wherein said polypeptide consists of SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:18, or SEQ ID NO:13 with the sample under conditions that allow polypeptide/antibody complexes to form;   (b) detecting polypeptide/antibody complexes;   wherein the detection of polypeptide/antibody complexes is an indication that PRSSV or a PRSSV polypeptide is present in the sample.   
     
     
         2 . The method of  claim 1 , wherein the one or more antibodies are monoclonal antibodies, polyclonal antibodies, or antibody fragments. 
     
     
         3 . The method of  claim 1 , wherein the sample is a biological sample, serum, whole blood, milk, meat juice, sputum, lung lavage fluid, lung tissue, tonsil tissue, or lymph node tissue. 
     
     
         4 . The method of  claim 1 , further comprising contacting the complexes of (a) with an indicator reagent comprising prior to the performance of (b). 
     
     
         5 . The method of  claim 4 , wherein the indicator reagent that generates a measurable signal. 
     
     
         6 . The method of  claim 1 , wherein the amount of PRRSV polypeptide or PRRSV in the test sample is determined. 
     
     
         7 . The method of  claim 1 , wherein the one or more antibodies are attached to a substrate. 
     
     
         8 . The method of  claim 1 , wherein the method comprises an assay selected from the group of assays consisting of a reversible flow chromatographic binding assay, an enzyme linked immunosorbent assay, a radioimmunoassay, a hemagglutination assay, a western blot assay, a fluorescence polarization immunoassay, and an indirect immunofluorescence assay.

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