Abstract: A method and system for handling media at a communication entity, wherein the media is associated with a communication session that is capable of entering an active state and an inactive state. The method comprises determining when the communication session is in an inactive state, causing the media associated with the communication session to be stored when the communication session has entered an inactive state, and causing the stored media to be conveyed to a user of the communication entity upon determination that the communication session has re-entered an active state.

Abstract: A method and system for handling media at a communication entity, wherein the media is associated with a communication session that is capable of entering an active state and an inactive state. The method comprises determining when the communication session is in an inactive state, causing the media associated with the communication session to be stored when the communication session has entered an inactive state, and causing the stored media to be conveyed to a user of the communication entity upon determination that the communication session has re-entered an active state.

Abstract: This invention relates generally to a method for quantifying the number of occurrences of a specific nucleic acid sequence within a nucleic acid sample in order to circumvent the shortcomings of the methods currently available and to provide reliable quantification of a specific nucleic acid sequence within a nucleic acid sample. The present invention provides a method of assessing an amount of a known target nucleic acid sequence in a sample comprising co-amplifying said target nucleic acid sequence and a known amount of a known control nucleic acid sequence to produce respective target and control amplicons, wherein said control nucleic acid sequence is different than said target nucleic acid sequence; and determining relative amounts of said respective amplicons by determining relative quantities of a primer extension reaction using each of said respective amplicons as a template.

Abstract: The present invention provides methods of identifying transformed plants using the restoration of male fertility as a selectable marker. Preferably, the fertility restorer genes are used to restore fertility in Brassica napus. The present invention also includes vectors comprising male sterility genes flanked by recombinase sites, vector comprising a fertility restorer gene and a nucleotide sequence of interest flanked by recombinase sites, and methods of using such vectors to produce transgenic plants, using restoration of male fertility as the selection for transformation events.

Abstract: The invention provides oligonucleotides and their complements that can be used as allele-specific probes or primers for sequencing, oligonucleotide probe hybridization, and allele-specific amplification. Such oligonucleotides can be used, for example, to facilitate genetic distinction between individual plants in plant populations.

Abstract: A smart card reader and transaction system which uses the voice path of a switched telephone network to effect smart card transactions are described. The smart card reader may be used with either a regular telephone or an ADSI telephone. If the telephone is not a handsfree set, the smart card reader is preferably connected between the base set and the handset. If the telephone is a handsfree model, the card reader is positioned between the base set and the switched telephone network. A smart card application server controls the smart card reader and switches it between a user mode and a card communications mode. Most applications software resides on the application server so that the smart card reader is simple to construct and inexpensive to manufacture. The advantage is a simple, portable, inexpensive yet reliable system adapted to be owned and used by the general public.

Abstract: The instant invention provides a method for detecting the presence of a restorer gene in the nuclear genomic DNA of a Brassica plant comprising the use of a probe/primer comprising the sequence of the Brassica glyceraldehyde-3-phosphate dehydrogenase (SEQ ID NO: 1) or a sufficient hybridizing fragment thereof.