Appeal No. 2003-1126 Page 11 Application No. 08/444,285 Claims 1 of the ’191 patent, which is not limited to any specific mammal or any specific gene, reads as follows: 1. A method of obtaining a mammal characterizes as having a plurality of cells containing exogenous genetic material, said material including at least one gene and a control sequence operably associated therewith, which, under predetermined conditions, express said gene under the control of said control sequence in a cell of said mammal, which comprises: (a) introducing exogenous material into a pronucleus of a mammalian zygote by microinjection, said zygote being capable of development into a mammal, said genetic material including at least one gene and a control sequence associated therewith, thereby obtaining a genetically transformed zygote; (b) transplanting an embryo derived from the genetically transformed zygote into a pseudopregnant female capable of bearing an embryo to term; (c) allowing the embryo to develop to term; where said gene and control sequence are selected so that the gene is not activated in such manner and degree as would prevent normal development of the embryo to term. What we understand the examiner’s argument to be is that, while the specification is enabling for a broad method of producing the claimed transgenic material, it does not teach one skilled in the art how to use the product. The panel does not agree that this is a proper distinction, however, i.e., that the amount of disclosure required to enable a product is higher than that required toPage: Previous 1 2 3 4 5 6 7 8 9 10 11 12 13 14 NextLast modified: November 3, 2007