Abstract:
Disclosed are methods and kits for analyzing a sample comprising 1,5-anhydroglucitol and a possible first analyte via one or more chemiluminescent reactions. Certain embodiments include measuring a first light response resulting from a first chemiluminescent reaction and measuring a second light response resulting from a second chemiluminescent reaction. Certain embodiments also include comparing the first light response to the second light response to determine a ratio of 1,5-anhydroglucitol and the first analyte. Also provided are kits including reagents for practicing the claimed methods.
Abstract:
The present disclosure provides devices, systems, kits and methods useful for quantitation of biomolecules such as intact proteins and nucleic acids.
Abstract:
A fluidic coupler to engage a plurality of flow cells of a sensor device includes a body and a plurality of fluidics interfaces formed in the body. Each fluidic interface of the plurality of fluidics interfaces includes an opening, a first port in fluid communication with the opening, a second port, and a third port in fluidic communication with the second port.
Abstract:
The present invention relates to a device and a method for evaluating performance of a deodorant using a superabsorbent polymer (SAP), and the device and method are capable of quantitatively evaluating deodorant performance by collecting ammonia adsorbed to deodorant materials including the SAP and measuring the amount of ammonia thereof.
Abstract:
Provided is an automatic analysis device that can suppress concentration of a reagent made to react with a specimen. This automatic analysis device is provided with: a reagent container which accommodates a reagent and which has attached thereto a perforable lid; a perforation unit for perforating the lid; and a reagent suction nozzle that is inserted into a hole formed by perforation and that sucks up the reagent. The automatic analysis device is characterized by being further provided with a state storage unit that stores the state as to whether the reagent container is in an unused state or in a used state, and a state update unit that, when the lid is perforated by the perforation unit while the reagent container is in an unused state, updates the state stored in the state storage unit to the used state.
Abstract:
A molecular detection apparatus according to a embodiment includes: a collection unit which collects detection target gases each containing molecule to be detected; a concentration adjusting unit which dilutes and/or concentrates the molecule, and generates a plurality of detection target gases having different concentrations of the molecule; a detection unit to which the plurality of detection target gases are sequentially introduced, and which includes a plurality of detection cells each outputting detection signals based on the concentrations of the molecule in the plurality of detection target gases; and a discrimination unit which discriminates the molecule by change tendencies of the detection signals based on the concentrations of the molecule.
Abstract:
A molecular detection apparatus according to a embodiment includes: a collection unit which collects detection target gases each containing molecule to be detected; a concentration adjusting unit which dilutes and/or concentrates the molecule, and generates a plurality of detection target gases having different concentrations of the molecule; a detection unit to which the plurality of detection target gases are sequentially introduced, and which includes a plurality of detection cells each outputting detection signals based on the concentrations of the molecule in the plurality of detection target gases; and a discrimination unit which discriminates the molecule by change tendencies of the detection signals based on the concentrations of the molecule.
Abstract:
A method, system, and apparatus for analyzing the concentrations and amounts of one or more different compounds comprises filling a chromatographic column with at least two packing materials in serial, inserting a mobile phase into the chromatographic column, injecting a sample compound into the chromatographic column, and determining at least one constituent compound in the sample compound as the sample compound elutes through the chromatographic column.
Abstract:
Linearization of an ionization detector is obtained by processing the output signal derived from the ionization detector so as to compensate for the naturally-occurring logarithmic decay of the detector response at high sample concentrations. Linearization is accomplished according to a linearizing formula:I.sub.(lin) =I[1+(I/I.sub.(dec))].sup.pwrwhere:I.sub.(lin) =linearized output signal current of the detectorI=non-linearized output signal current of the detectorI.sub.(dec) =output signal current at onset of logarithmic decaypwr=a power factor that compensates for the slope of the logarithmic decay
Abstract:
An electron capture detector has a detection cell containing an electrode and a radioactive isotope for ionizing a carrier gas and causing electrons to be emitted. Before the detection cell begins to be contaminated, a pulse voltage is applied to the electrode and the frequency of this pulse voltage is controlled by a loop control routine to find an initial pulse frequency value such that a current through the electrode due to the emitted electrons comes to have a specified current value as a carrier gas is introduced into the detection cell. When a sample is analyzed after the detection cell becomes contaminated, the same process is carried out before the sample is injected and a pre-measurement pulse frequency value is obtained. After the sample is injected, the same process is repeated to obtain a measured pulse frequency value. The concentrations of components of the sample are calculated from the measured pulsed frequency value, and the effects of contamination of the detection cell are removed by considering both the initial and pre-measurement pulse frequency values.