Abstract: The following embodiments generally relate to the use of a “swap area” in a non-volatile memory as an extension to volatile memory in a computing device. These embodiments include techniques to use both volatile memory and non-volatile swap memory to pre-load a plurality of applications, to control the bandwidth of swap operations, to encrypt data stored in the swap area, and to perform a fast clean-up of the swap area.

Abstract: The following embodiments generally relate to the use of a “swap area” in a non-volatile memory as an extension to volatile memory in a computing device. These embodiments include techniques to use both volatile memory and non-volatile swap memory to pre-load a plurality of applications, to control the bandwidth of swap operations, to encrypt data stored in the swap area, and to perform a fast clean-up of the swap area.

Abstract: The following embodiments generally relate to the use of a “swap area” in a non-volatile memory as an extension to volatile memory in a computing device. These embodiments include techniques to use both volatile memory and non-volatile swap memory to pre-load a plurality of applications, to control the bandwidth of swap operations, to encrypt data stored in the swap area, and to perform a fast clean-up of the swap area.

Abstract: The following embodiments generally relate to the use of a “swap area” in a non-volatile memory as an extension to volatile memory in a computing device. These embodiments include techniques to use both volatile memory and non-volatile swap memory to pre-load a plurality of applications, to control the bandwidth of swap operations, to encrypt data stored in the swap area, and to perform a fast clean-up of the swap area.

Abstract: The following embodiments generally relate to the use of a “swap area” in a non-volatile memory as an extension to volatile memory in a computing device. These embodiments include techniques to use both volatile memory and non-volatile swap memory to pre-load a plurality of applications, to control the bandwidth of swap operations, to encrypt data stored in the swap area, and to perform a fast clean-up of the swap area.

Abstract: The following embodiments generally relate to the use of a “swap area” in a non-volatile memory as an extension to volatile memory in a computing device. These embodiments include techniques to use both volatile memory and non-volatile swap memory to pre-load a plurality of applications, to control the bandwidth of swap operations, to encrypt data stored in the swap area, and to perform a fast clean-up of the swap area.

Abstract: The following embodiments generally relate to the use of a “swap area” in a non-volatile memory as an extension to volatile memory in a computing device. These embodiments include techniques to use both volatile memory and non-volatile swap memory to pre-load a plurality of applications, to control the bandwidth of swap operations, to encrypt data stored in the swap area, and to perform a fast clean-up of the swap area.

Abstract: A water-soluble reference standard is useful for immunoassays of a lipophilic drugs. The reference standard is a compound of formula (I): G-(L)n—Y;??(I) where G is a lipophilic drug; L is a linker which is an alkyl group or heteroalkyl group containing from 1 to 20 carbon atoms; n is 0 or 1; and Y is a water-solubilizing group such as —SO3?, —NR—SO3?, —P(?O)(OH)(O?), or —O—P(?O)(OH)(O?); where R is H or an alkyl group of 1 to 10 carbon atoms.

Abstract: A water-soluble reference standard is useful for immunoassays of a lipophilic drugs.

Abstract: An immunoassay method based upon inhibition of a DNA polymerase enzyme accomplished by linking a ligand of the analyte to a primer through a covalent bond. The interaction between the primer-bound ligand and a receptor specific for the ligand inhibits the DNA polymerase enzyme from generating double stranded DNA. The degree of inhibition of double stranded DNA synthesis is inversely proportional to the concentration of analyte in the sample. The analyte is determined by measuring the formation of double stranded DNA, e.g., by a fluorescence DNA intercalation technique.

Abstract: A protein containing at least one pendant sulfhydryl group is directly radiolabeled with a radiometal which binds tightly to sulfhydryl groups, using one or more pendant sulfhydryl groups on the protein as endogenous ligands and optionally using an exogenous ligand which binds tightly to the radiometal ion to further stabilize the chelate.

Abstract: A protein containing at least one pendant sulfhydryl group is directly radiolabeled with a radiometal which binds tightly to sulfhydryl groups, using one or more pendant sulfhydral groups on the protein as endogenous ligands and optionally using an exogenous ligand which binds tightly to the radiometal ion to further stabilize the chelate.