Abstract: A calibration standard for calibrating machines which count the somatic cells in a milk sample, comprises an aqueous dispersion of microbeads bearing a fluorescent dye, a suspending agent, and an electrolyte; the dye has an excitation wavelength below 580 nm and a fluorescence emission wavelength in the range of 550 to 660 nm, with the excitation wavelength being at least 10 nm below the emission wavelength; the microbeads are present in a predetermined number per unit volume of dispersion; typically the standard contains 1.times.10.sup.5 to 9.times.10.sup.5 beads/ml.

Abstract: A method and apparatus for calibrating or checking the calibration of vertical photometers. The invention may also provide easy and convenient assay results for diagnostic profiles. The invention comprises pre-dispensed amounts of a suitable reagent, chosen for the particular use, disposed in a vessel with an amount of a wetting agent or other means to yield a reproducible meniscus in the resulting control solution. The control solution is dried to leave a precise amount of dried reagent and other constituents in the vessel which can then be stored and distributed until subsequent use. The dried control solution can then be reconstituted to provide a standard having known absorbance and physical characteristics.

Abstract: A method and kit for estimating the amount of methyl anthranilate includes obtaining a sample suspected of having methyl anthranilate, acidifying the sample with a strong acid, adding sodium nitrite to the acidified sample producing nitrous acid which in the presence of methyl anthranilate produces a diazonium ion. The method further comprises a step of adding sulfamic acid which removes excess nitrous acid from the sample, followed by the addition N-(1-naphthyl) ethylenediamine which reacts with the diazonium ion to form a colored complex which is color responsive which is then compared to standards prepared using known amounts of methyl anthranilate. The kit provides the a sample holder and vials of ingredients and standards to practice the method.

Abstract: A method for producing a liquid phase substance having a pre-established concentration of CO.sub.2 suitable for calibrating analytical instruments such as hemogasanalyzers consists in:preparing an aqueous solution of precisely known strength of a water-soluble salt of carbonic acid,then transferring said solution to a flow reactor containing a cation exchange resin in hydrogenionic form,passing the aforesaid solution of carbonic acid salt through the aforesaid cation resin,thereby achieving the reaction of producing a pre-established quantity of CO.sub.2, andtransferring the eluate thus obtained directly to the analytical instrument for calibration.

Abstract: A formulation of combined-composition electrolyte and pH buffers for use as standardization solutions in analyzers for clinical chemistry which simultaneously use more than one ion-selective electrode plus more than one standard solution. Each ion is present in the standard solution in stoichiometric quantity such as to compensate the effect due to the incomplete dissociation of the salt used, and to obtain an activity coefficient and liquid junction potential such as to reduce the error generated by the use of standardization solutions which do not take account of these quantities. Buffer solutions are described having a pH within the range of 6-8 and an electrolyte compositions (Na.sup.+, K.sup.+, Ca.sup.+ and Cl.sup.-) which reflect the composition of the biological liquid to be analyzed, namely whole blood, plasma or serum, in equilibrium with different partial pressures of oxygen and CO.sub.2.

Abstract: In an automated analyzer that measures concentration of samples by comparing changes in a detector response caused by said samples to a calibration curve or factor based on one or more different calibration standards stored in the analyzer, a replacement calibration standard is validated automatically by processing a portion of said replacement calibration standard as a sample prior to accepting the new calibration standard as a valid standard.

Abstract: A method and device for calibrating or checking the calibration of vertical photometers. The invention may also provide easy and convenient assay results for diagnostic profiles. The invention comprises pre-dispensed amounts of a suitable reagent, chosen for the particular use, disposed in a vessel with an amount of a wetting agent to yield a reproducible meniscus in the resulting control solution. The control solution is dried to leave a precise amount of dried reagent and other constituents in the vessel which can then be stored and distributed until subsequent use. The dried control solution can then be reconstituted to provide a standard having known absorbance and physical characteristics.

Abstract: A stabilizer for maintaining a constant level of CO.sub.2 in coenzyme containing enzymatic CO.sub.2 diagnostic reagents is disclosed, comprising rate-limiting amounts of (a) the diagnostic reagents and (b) coenzyme-regenerating reagents, e.g., wherein (a) is malate dehydrogenase, phosphoenolpyruvate carboxylase and NADH, and (b) is glucose dehydrogenase and glucose, as are methods of use and kits containing a diagnostic reagent and stabilizer.

Abstract: Aqueous acidic ferrioxalate compositions are disclosed for use as calibrants of pCO2 and of PO2 after photodecomposition. Compositions with high iron(III) to oxalate molar ratios (e.g., 5:1 to 100:1 with 0.3 to 15 millimolar oxalate) produce carbon dioxide on exposure without oxygen consumption. Compositions with low iron(III) to oxalate ratios (e.g., 1:100 to 1:2000) with 0.1 to 5 millimolar iron(III) produce carbon dioxide on exposure with concurrent oxygen consumption. Use of the two types of compositions enables calibration values to be established with varying pCO2 values and with, respectively, high and low pO2 values.

Abstract: A liquid control standard for the use in the quality assurance of blood analysis instrumentation systems is disclosed. The liquid control standard is able to act as a control standard for blood gas instrumentation systems measuring pH, pCO.sub.2 and pO.sub.2 of blood, as a liquid control standard for ion selective electrode instrumentation systems for the measuring of electrolytes such as ionized calcium and total calcium as well as Na, K and Li ions in the blood and, optionally, as a control standard for a co-oximeter measuring the amount of total hemoglobin present in the blood and the relative amounts of other hemoglobin fractions present in the blood.

Abstract: A liquid control standard for the use in the qualilty assurance of blood analysis instrumentation systems is disclosed. The liquid control standard is able to act as a control standard for blood gas instrumentation systems measuring pH, pCO.sub.2 and pO.sub.2 of blood, as a liquid control standard for ion selective electrode instrumentation systems for the measuring of electrolytes such as ionized calcium and total calcium as well as Na, K and Li ions in the blood and, optionally, as a control standard for a co-oximeter measuring the amount of total hemoglobin present in the blood and the relative amounts of other hemoglobin fractions present in the blood.

Abstract: A reference liquid for calibration or quality control of instruments which determine ionized calcium and pH. The reference liquid contains both a particular calcium ion activity and a pH-buffer and can therefore be used for calibration of both the calcium-sensitive electrode and the pH-electrode in the instruments. The pH-buffer is a nitrogen-containing organic sulphonic acid and the salt of this acid, the acid having a pK in the range of 6.6-7.6. The reference liquid has an ionic strength of 0.15-0.17, a buffer capacity .beta. in the range of 0.04-0.10 and is packed in glass ampoules.

Abstract: A method for determining the wavelength accuracy of a variable wavelength liquid chromatography detector in the low UV range comprising filling the cell of the detector with a test solution and varying the indicated wavelength of detection to find the indicated wavelength of maximum absorbance in a wavelength region around a reference wavelength of the test solution and then calculating the difference between the indicated wavelength of maximum absorbance and the reference wavelength to determine the accuracy of the indicated wavelength of the detector. The test solution contains terbium III ions in a solvent such as n-propanol so that the absorbance maximum of the test solution does not shift more than about 0.5 nm for a spectral bandpass ranging from 2 to 6 nm.

Abstract: An agent and process are used for the determination of calcium in liquids. The agent contains essentially orthocresolphthalein complexone, an acid and a zwitterionic buffer and is characterized in that the buffer contains at least one sulphonic acid amine of the general formula ##STR1## wherein R.sub.1 and R.sub.2 are identical or different and denote H or alkyl, hydroxyalkyl or cycloalkyl having in each case up to 8 C atoms andR.sub.3 denotes alkyl or hydroxyalkyl having up to 8 C atoms.

Abstract: A method of calibrating a flow cytometer or fluorescent microscope is based on a set of highly uniform microbeads associated with a fluorescent dye in such a way that the microbeads have the same excitation and emission spectral properties as the samples which are to be measured. The calibration values of the microbeads are plotted against the relative fluorescence intensity peak channel or intensity reading for each microbead in the set. From this calibration plot, the relative fluorescence intensity peak channel or intensity reading of the sample is translated into equivalent soluble fluorescent dye molecules per sample particle. The calibration values of the standard microbeads are determined against solutions of the dyes.

Abstract: This invention discloses a multiple control standard for the use in the quality assurance of blood analysis instrumentation systems. The liquid control standard is able to act as a control standard for blood gas instrumentation systems measuring pH, pCO2 and pO.sub.2 of blood, as a control standard for a co-oximeter measuring the amount of total hemoglobin present in the blood and the relative amounts of other hemoglobin fractions present in the blood, and as a liquid control standard for ion selective electrode instrumentation systems for the measuring of electrolytes such as Na, K, Li and Ca ions in the blood.

Abstract: A calibration liquid, especially suitable for ion-selective electrodes, containing albumin. This solution is stable and prevents errors by junction potentials or unknown complexing with calcium.

Abstract: This invention discloses a multiple control standard for the use in the quality assurance of blood analysis instrumentation systems. The liquid control standard is able to act as a control standard for blood gas instrumentation systems measuring pH, pCO2 and pO.sub.2 of blood, as a control standard for a co-oximeter measuring the amount of total hemoglobin present in the blood and the relative amounts of other hemoglobin fractions present in the blood, and as a liquid control standard for ion selective electrode instrumentation systems for the measuring of electrolytes such as Na and K ions in the blood.

Abstract: A method of calibrating a flow cytometer or fluorescent microscope is based on a set of highly uniform microbeads associated with a fluorescent dye in such a way that the microbeads have the same excitation and emission spectral properties as the samples which are to be measured. The calibration values of the microbeads are plotted against the relative fluorescence intensity peak channel for each microbead in the set. From this calibration plot, the relative fluorescence intensity peak channel of the sample is translated into equivalent soluble fluorescent dye molecules per sample particle. The calibration values of the standard microbeads are determined against solutions of the dyes.

Abstract: A method and structure for mounting fluorescent samples, e.g., fluorescent microbeads, are based on immobilizing the samples in a gel which preserves the spectral properties of the samples and mounting the gel containing the samples on a slide and beneath a coverslip.

Abstract: The article includes a first vial (12) which is positioned within a second larger vial (32). The first vial (12) separately contains a first fluid, such as a first calibrating fluid, and the second vial (32) contains a second fluid, such as a second calibrating fluid. A stopper (18) seals the first vial (12) and holds a sensing portion (21) of the sensor in the first vial (12). The first vial (12) is released from the second vial (32) by activating a plunger (36).An encapsulation package (50) having first and second elements (51, 52) maintains the chemical sensor and a calibrating article or vessel in a sterile condition. The package includes a first cavity (54) which receives the calibrating vessel, the sensing portion of the sensor and a substantial portion of the sensor cable, and a second cavity (56) which receives the sensor connector. A passageway (58) connecting the two cavities (54, 56) is adapted to receive a portion of the sensor cable.

Abstract: A process for determining the composition of an aqueous solution of ammonia and carbon dioxide from which ammonium carbamate or ammonium carbonate crystallizes out upon cooling to below the saturation temperature. The density and the saturation temperature of the solution are measured, and the ammonia, carbon dioxide, and water composition is determined by reference to densities and saturation temperatures of aqueous solutions of ammonia and carbon dioxide of known composition. The composition thus determined can be used to effect control over the composition of such aqueous solutions.

Abstract: A wavelength calibration solution comprising from about 0.025 to about 0.140 molar neodymium and from about 0.135 to about 0.550 molar samarium, wherein the neodymium is present as a neodymium ionized constituent and the samarium is present as a samarium ionized constituent.A method for checking the wavelength accuracy of spectrometers or spectrophotometers of the type comprising measuring the absorbance (A) or percent transmittance (% T) of a wavelength calibration check solution versus a blank at more than one wavelength. The method is characterized in that the above solution is employed therein as the wavelength calibration check solution.

Abstract: An aqueous reagent for determining inorganic phosphate in a protein-containing liquid biological sample comprises a molybdate salt, an acid capable of reacting with the molybdate salt to form molybdic acid for complexation with phosphate to form phosphomolybdate complexes, a ferric salt in an amount sufficient to inhibit turbidity in the sample, and a nonionic surfactant reagent in an amount sufficient to further inhibit turbidity in the sample, the molybdate salt and the acid being present in amounts sufficient to form an amount of molybdic acid sufficient to produce a detectible color change when complexed with phosphate in the sample.

Abstract: A solution of the type comprising cobalt ammonium sulfate and sulfuric acid. The solution is characterized in that it comprises from about 0.020 to about 0.040 N H.sub.2 SO.sub.4.Also, a method for checking the linearity of response of a spectrometer or spectrophotometer. The method is of the type comprising measuring absorbance (A) or percent transmittance (%T) of a solution versus a blank at a known wavelength. The method is characterized in that the above solution is employed therein.In addition, a method for checking photometric accuracy of a spectrometer or spectrophotometer. The method is of the type comprising measuring A or %T of a solution at a specific wavelength. The method is characterized in that the above solution is employed therein.

Abstract: In the reference electrode for the oxygen probe comprising a mixture of Cr powder and Cr.sub.2 O.sub.3 powder, an improved reference electrode characterized in that Cr powder and Cr.sub.2 O.sub.3 powder are mixed in a ratio 97%:3% to 80%:20% and the mixture is sintered beforehand. An oxygen probe using this electrode exhibits improved response, stability and reproducibility in molten steel.

Abstract: A reference liquid for calibration or quality control of instruments which determine ionized calcium and pH. The reference liquid contains both a particular calcium ion activity and a pH-buffer and can therefore be used for calibration of both the calcium-sensitive electrode and the pH-electrode in the instruments. The pH-buffer is a nitrogen-containing organic sulphonic acid and the salt of this acid, the acid having a pK in the range of 6.6-7.6. The reference liquid has an ionic strength of 0.15-0.17, a buffer capacity .beta. in the range of 0.04-0.10 and is packed in glass ampoules.