Radiation Effects on Concentrated Potassium Hexacyanoferrate(III) Solutions

The neutron irradiated potassium hexacyanoferrate(III) solutions were analyzed for Fe(CN)₆^4?, Fe(CN)₆^3?, and Prussian blue. The retention values (1.1%) were constant throughout the pH and concentration ranges studied, and did not change with the length of irradiation. The complex behavior of the radiochemical yield of the Fe(CN)₆^4? and Prussian blue was attributed to the competition of the various reactions involved in the irradiation.     

Strong-coupling effects in high-T c superconductors

It is conceivable that the high-T _c superconducting perovskites are conventional electronphonon superconductors. In this case one expects significant strong-coupling effects because of the unusually high ratiok _B T _c / of the order 0.1 and greater. We use a set of reasonable models for the Eliashberg function ² F() (which takes into account available information on the phonon spectra and which fit the measuredT _c 's) and calculate strong-coupling effects in the specific heatc _s (T)/T _c , the ratio ₀/k _B T _c , the critical fieldsH _c (T) andH _c2 (T) including Pauli limiting, and other measurable quantities. Strongcoupling corrections turn out to be in the range of 0 to about 100%, depending on the quantity of interest. We discuss the perspectives of using strong-coupling effects as indicators for conventional electron-phonon superconductivity in the new materials.     

Rapid flow-injection sandwich-type immunoassays of proteins using an immobilized antibody reactor and adenosine deaminase-antibody conjugates

A rapid flow-injection sandwich enzyme immunoassay suitable for the direct determination of proteins in biological samples is described. The proposed system utilizes highly active adenosine deaminase—antibody conjugates in conjunction with a flow-through immunoreactor and an ammonium ion-selective potentiometric detector. After appropriate sample/reagent injection steps, the enzyme activity bound to the reactor is measured by diverting a coninuously flowing stream of substrate (adenosine) through the packed immunocolumn and detecting liberated ammonium ions downstream with a tubular ammonium ion-selective electrode. The bound enzyme activity is directly proportional to the concentration of analyte in the original sample. By using non-equilibrium flow-rates of sample and reagent slugs, a single protein assay takes less than 12 min, including regeneration of the reactor. The proposed method is shown to be selective, reproducible and capable of determining accurately the model protein (human IgC) at sub-μg ml^?1 concentrations.     

Rapid and sensitive silver-lipopolysaccharide staining using PhastSystem in fast horizontal polyacrylamide gel electrophoresis

A rapid and sensitive silver-lipopolysaccharide staining method has been developed by using PhastSystem. The total time of the procedure (including time of Phastgel electrophoresis) is within 2 h. It is at least 10 times faster than the previous reported methods and the sensitivity is also increased.