Ex Parte Ridgway - Page 3

                Appeal  2006-2372                                                                                  
                Application 10/854,708                                                                             
                       The rejections as presented by the Examiner are as follows:                                 
                1.  Claims 1-3, 8-11, 14, 18, 20, and 21 stand rejected under 35 U.S.C. § 35                       
                U.S.C § 103(a) as unpatentable over Jennings.                                                      
                2.  Claims 6, 7, 12, 13, 15-17, and 19 stand rejected under 35 U.S.C. § 35                         
                U.S.C § 103(a) as unpatentable over the combination of Jennings and Brady.                         
                       We affirm.                                                                                  

                                                 DISCUSSION                                                        
                       The claims have not been argued separately and therefore, for each                          
                ground of rejection, the claims will stand or fall together.  37 C.F.R. §                          
                41.37(c)(1)(vii).  Therefore, we limit our discussion to representative claims                     
                1 and 6.                                                                                           

                Claim 1:                                                                                           
                       Claim 1 is drawn to a method for measuring platelet function.  The                          
                method comprises five steps:                                                                       
                       i. obtaining a baseline count of platelets in a sample.  Claim 1                            
                                 defines the sample as one that comprises platelets in a liquid                    
                                 medium obtained from a physiological source of the                                
                                 platelets, which is devoid of an effective amount of an agent                     
                                 which interferes with platelet function;                                          
                       ii. adding an activation agonist to the sample after the baseline                           
                                 count is performed;                                                               
                       iii. allowing activatable platelets in the sample to activate;                              
                       iv. obtaining a count of the unactivated platelets in the sample                            
                                 from step iii; and                                                                

                                                        3                                                          

Page:  Previous  1  2  3  4  5  6  7  8  9  Next

Last modified: September 9, 2013