Abstract: An assay for photometrically detecting and/or quantitating the presence of an analyte in a sample in which the signal generated by a label associated with the analyte is photometrically detected in the presence of a suspended solid support.

Abstract: An immunoassay for CK isoenzyme or CK isoform is provided based on capture of the CK isoenzyme or CK isoform by a specific antibody immobilized through a cleavable linker containing a disulfide bond onto a solid phase and release of the resulting antibody-CK isoenzyme or antibody-CK isoform complex by the addition of a reducing agent to cleave the disulfide bond and simultaneously activate the CK isoenzyme or CK isoform.

Abstract: Immunoassays and DNA probe assays utilizing a non-immune, reversible binding displacement system are provided. In the assay, a releasable ligand, a binding partner for the releasable ligand, an analyte of interest, an analytically detectable (reporter) group, and at least one binding partner for the analyte, are first attached to an insoluble phase so as to form reporter-labeled complex bound to an insoluble phase, followed by the addition of a displacer ligand which displaces the releasable ligand along with some portion of the reporter-labeled complex, so that the released reporter is analytically detectable in a free liquid medium and can be related to the concentration of analyte in the sample.

Abstract: In situ process for production of conjugates using a deblocking agent which allows conjugation to occur and two compositions wherein one composition is functionalized with a group capable of reacting efficiently with free thiols, and a second composition containing blocked thiols.

Abstract: An oxalate oxidase can be extracted from the stems of beet by homogenizing the beet, filtering, centrifuging the filtrate, precipitating the oxalate oxidase containing fraction with acetone, dissolving the precipitate in taurodeoxycholic acid, dialyzing the solution and column chromatography. Unlike prior art oxalate oxidase compositions, the instant composition is relatively insensitive to sodium chloride and is well adapted to rapid and inexpensive oxalate assay in body fluids. The composition is inactive on almost all body fluid components other than oxalate, the only significant interfering component being ascorbate, and this ascorbate is readily removed by treatment with acid ferric chloride prior to the oxalate oxidase assay procedure, the ferric ion being thereafter removed by a cation exchange resin.