The invention relates to a new method of characterising a target ribonucleic acid (RNA) involving forming a complementary polynucleotide. The method uses a transmembrane pore.

Peroxycarboxylic acid compositions comprising compatible ionic compounds to deliver conductivity signals to enable monitoring of the peroxycarboxylic acid concentration by conductivity when diluted for use are disclosed. Methods of measuring peroxycarboxylic acid concentration by conductivity are also disclosed. Beneficially, conductivity measurement allows a user to determine concentration of the peroxycarboxylic acid at a point of use without cumbersome titration steps to determine the concentration providing various benefits at an application of use.

A measuring device includes: a first electrode immersed in sample water stored in a measuring tank; a second electrode immersed in the sample water; and a controller that: causes a power source to flow a current through the sample water between the first electrode and the second electrode; detects, based on a first digital signal, an interruption whereby an analog signal fluctuates by no less than a predetermined value; and calculates, based on a second digital signal, a concentration of a measurement target in the sample water. The first digital signal is acquired by sampling the analog signal with a first sampling period. The analog signal is based on the current flowing through the sample water. The second digital signal is acquired by sampling the analog signal with a second sampling period that is longer than the first sampling period.

The present invention relates to sample analysis cartridges comprising micro-environment sensors and methods for assaying coagulation in a fluid sample applied to the micro-environment sensors, and in particular, to performing coagulation assays using micro-environment sensors in a point of care sample analysis cartridge. For example, the present invention may be directed to a sample analysis cartridge including an inlet chamber configured to receive a biological sample, and a conduit fluidically connected to the inlet chamber and configured to receive the biological sample from the inlet chamber. The conduit may include a micro-environment prothrombin time (PT) sensor, and a micro-environment activated partial thromboplastin time (aPTT) sensor.

The present disclosure relates to an electrode of an electrochemical measuring system and includes a housing having a chamber in which an electrolyte is arranged, and a potential-forming element which is at least partially arranged in the chamber such that the electrolyte at least partially wets the potential-forming element. A discharge line is made of coinage metal or of an alloy comprising a coinage metal and contacts the potential-forming element. A closure element closes the housing and guides discharge line therethrough. An adhesion promoter which comprises a glass and/or a glass-ceramic material and is arranged between the closure element and the discharge line.

Bioelectrochemical Systems (BES) for use as Biological Oxygen Demand (BOD) sensors, systems incorporating BES sensors for measuring BOD, and methods of using the sensors and systems for measuring BOD. The disclosed sensors are inexpensive to construct, long-lasting, have a fast response, and a large dynamic range. The invention includes biological oxygen demand (BOD) sensors which incorporate at least three working electrodes, at least one counter electrode, a reservoir for dilution fluid, and a sensor for measuring an electric current or a voltage which flows from the working electrodes to the counter electrode. The BOD sensors will typically also include at least one electrically active microbe disposed in proximity to the working electrode.

An electrolyte concentration measurement device includes: an ion-selective electrode supplied with the liquid; a reference electrode serving as a reference for a potential; a potential measuring unit configured to acquire a potential of the ion-selective electrode; a concentration calculation unit configured to calculate a concentration of ions contained in the liquid based on the potential acquired by the potential measuring unit; a potential monitoring unit configured to monitor a potential of the ion-selective electrode and generate a potential response curve; a timing signal acquisition unit configured to acquire a timing signal related to a timing of various operations; and a potential response curve analysis unit configured to detect an abnormality sign of a device based on a relationship between the potential response curve and the timing signal.

The invention relates to a new method of characterising a target ribonucleic acid (RNA) involving forming a complementary polynucleotide. The method uses a transmembrane pore.

The present disclosure relates to a method for producing an exchangeable electrode assembly, with at least one sensor body and at least a first electrode, for an electrochemical sensor for determining the concentration of an analyte in a gaseous or liquid measurement medium, a corresponding electrode assembly, and an electrochemical sensor with an electrode assembly according to the present disclosure. In order to produce the electrode assembly, the following method steps are performed: providing a sensor body, and applying at least a first electrically-conductive material to a first sub-region of the sensor body for producing a first electrode of the electrode assembly.

Provided is a method for measuring a component of a biological sample with a biosensor provided with: a capillary for introducing the biological sample; an electrode part including a first electrode system that includes a first working electrode and a first counter electrode in the capillary; and a reagent part disposed so as to be in contact with the electrode part, the reagent part containing an enzyme and a mediator, and the method including a step of starting voltage application for a duration longer than 0 second and up to 0.7 second to the first electrode system within 0 second to 0.5 second after detection of the introduction of the biological sample to obtain a hematocrit value based on a current value obtained thereby.