Ex parte TERSTAPPEN et al. - Page 3




              Appeal No. 1997-2391                                                                                      
              Application 08/239,265                                                                                    


              Kansas et al. (Kansas), “Expression of the CD11/CD18, Leukocyte Adhesion Molecule 1,                      
              and CD44 Adhesion Molecules During Normal Myeloid and Erythroid Differentiation in                        
              Humans,” Blood, Vol. 76, No. 12, pp. 2483-492 (Dec. 1990)                                                 
                     Claims 1 through 7, 10 through 13, 15 and 16 stand rejected under 35 U.S.C.     §                  
              103 as unpatentable over Loken and Kansas.  Claims 8 and 9 stand rejected under 35                        
              U.S.C. § 103 as unpatentable over Loken, Kansas and Basch.  We reverse both                               
              rejections.                                                                                               
                                                    DISCUSSION                                                          
                     Claim 1, directed to multi-parameter analysis of cells in body fluid, represents the               
              invention in its broadest aspect: erythrocyte precursors and proliferating cells, among                   
              others, are identified and counted based on differential light scatter and differential binding           
              of a fluorescent nucleic acid dye, a first monoclonal antibody specific for an antigen                    
              differentially expressed on the cells, and a second monoclonal antibody specific for an                   
              antigen differentially expressed on erythrocyte precursors and proliferating cells (the two               
              antibodies have fluorescent labels with peak emission spectra different from each other                   
              and from the nucleic acid dye).  The two antibodies are described in functional terms in                  
              claim 1, but there is no requirement that they recognize any antigen in particular.                       
              Nevertheless, both the examiner and appellants have focused throughout the prosecution                    
              on that embodiment of the method wherein the first fluorescently-labeled monoclonal                       
              antibody is specific for CD45 and the second is specific for CD71 (as required in claims                  


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