Ex Parte Ilsley et al - Page 2


             Appeal No. 2006-1547                                                              Page 2                
             Application No. 10/114,668                                                                              

             hybridized to a target nucleic acid analyte.  Specification, ¶ 6.  In addition to the DNA               
             primer, a DNA polymerase, dNTPs, and other reactants required for DNA synthesis can                     
             be present at the distinct locations which comprise the array.                                          


                                                    Discussion                                                       
             1.  Claim construction                                                                                  
                    Claims 1-39 are on appeal.  The claims do not stand or fall together.  Appellant                 
             presented arguments for three separate groups of claims.  Appeal Brief, page 11.  We                    
             consider the following claims representative of the claims subject to each rejection:                   
                    Group I                                                                                          
                    1. A method of assaying a sample for the presence of one or more nucleic acid                    
                    analyte members of a nucleic acid analyte set, said method comprising:                           
                    (a) providing an array of at least two distinct DNA primer compositions                          
                    immobilized on a surface of a solid support at distinct locations, wherein each of               
                    said at least two distinct DNA primer compositions comprises a DNA primer that                   
                    hybridizes under stringent conditions to a different member of said nucleic acid                 
                    analyte set and at least one template dependent primer extension reactant                        
                    comprising a pulse-jet deposited polymerase;                                                     
                    (b) contacting each of said at least two distinct DNA primer compositions of said                
                    array with said sample under DNA synthesis conditions sufficient to produce                      
                    labeled target nucleic acids at locations on said surface where a nucleic acid                   
                    analyte present in said sample hybridizes to a DNA primer to produce a duplex                    
                    nucleic acid;                                                                                    
                    (c) detecting the presence of labeled target nucleic acids on said array surface to              
                    obtain assay data; and                                                                           
                    (d) employing said assay data to determine the presence of one or more nucleic                   
                    acid analytes in said sample.                                                                    
                    Group II                                                                                         
                    8. The method according to Claim 1, wherein said providing step comprises                        
                    providing an array of DNA primer compositions in a dry, storage stable format,                   
                    wherein each DNA primer composition includes: (a) a DNA primer; (b) pulse-jet                    
                    deposited polymerase; and (c) at least one of an effective amount of a DNA                       
                    synthesis reagent selected from the group consisting of: (i) dATP; (iii) [sic] dGTP;             
                    (iii) dTTP; (iv) dCTP; and (v) at least one type of labeled dNTP.                                






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