Appeal 2007-2517 Application 10/311,196 aspect of the enablement requirement of 35 U.S.C. § 112, first paragraph. In re Fouche, 439 F.2d 1237, 1243, 169 USPQ 429, 434 (CCPA 1971) (If “compositions are in fact useless, appellant’s specification cannot have taught how to use them.”); MPEP 2164.07 (Edition 8, August 2001; revised August 2006). Because we have found that the claims do not meet the utility requirement, we also are compelled to find that they do not meet the how to use requirement of 35 U.S.C. § 112. We affirm the rejection of claim 1; claims 2-7, 9, 11, 16, and 17 fall with claim 1 because they were not separately argued. Written description rejection Claim 1-7, 9, 11, 16, and 17 stand rejected under § 112, first paragraph, as failing to comply with the written description requirement for the limitation of “a polypeptide comprising at least 500 continuous amino acids of SEQ ID NO: 2, wherein the polypeptide has taste-specific receptor activity” (Answer 6). The Examiner contends that the limitation is “new matter,” not supported by the application as it was filed (Answer 6). We have found that the Specification does not disclose that SEQ ID NO: 2 is a polypeptide possessing taste-specific receptor activity. “To fulfill the written description requirement, the patent specification ‘must clearly allow persons of ordinary skill in the art to recognize that [the inventor] invented what is claimed.’ In re Gosteli, 872 F.2d 1008, 1012, 10 USPQ2d 1614, 1618 (Fed. Cir. 1989). An applicant complies with the written description requirement ‘by describing the invention, with all its claimed limitations.’ Lockwood v. American Airlines, Inc., 107 F.3d 1565, 1572, 41 USPQ2d 1961, 1966 (1997).” Gentry Gallery v. The Berkline Corp., 9Page: Previous 1 2 3 4 5 6 7 8 9 10 11 12 Next
Last modified: September 9, 2013