Ex Parte ALIZON et al - Page 11




              Appeal No. 1997-2528                                                                                      
              Application No. 07/810,908                                                                                

              the claimed p12, X protein, TAT and ART polypeptides.  Thus, appellants cannot rely                       
              on the filing date of Serial No. 06/835,228 of March 3, 1986 to support the written                       
              description requirement under § 112 for the present claims.                                               
              Claim 45                                                                                                  
                     Claim 45 is dependent upon claim 44 and further requires that the formation of                     
              an antigen-antibody complex is detected by a process selected from the group                              
              consisting of radioimmunoassay, radioimmunoprecipitation assay, immunofluorescense                        
              assay, enzyme linked immunosorbent assay, and Western blot, which is disclosed in                         
              Clavel at pages 344-345, and Figures 2 and 3.                                                             
              Claim 46                                                                                                  
                     Claim 46 is rejected under 35 U.S.C. § 103 over Clavel in view of Luciw.  Clavel                   
              describes an the use of peptides from the envelope portion of LAV-2 for use in ELISA,                     
              Western blot and radioimmunoprecipitation assays.  Clavel, page 344.  It would have                       
              been obvious to one of ordinary skill in the art at the time of the present invention to                  
              provide the components of such a known assay in a diagnostic kit for the detection of                     
              antibodies in a biological sample which bind to Human Immunodeficiency Virus Type 2                       
              in view of the desirability in the art to determine the presence of HIV antibodies in                     
              patient samples (Clavel, page 346) and general knowledge in the art of the                                
              convenience of immunoassay diagnostic test kits.  See, for example, Luciw, U.S. Patent                    
              No. 5,156,949 describing an article of manufacture for use in an immunoassay for the                      
              detection of Human Immunodeficiency Virus (claim 17).                                                     
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