Electrophoresis device including: a first flow passage extending in a first direction and through which a sample and a buffer solution flow; a sample collecting part provided at an end portion of the first flow passage and configured to collect the sample; electrodes disposed at both sides of the first flow passage in a second direction perpendicular to the first direction and configured to apply a voltage to the first flow passage in the second direction; second flow passages communicating with both sides of the first flow passage in the second direction, configured to accommodate the electrodes, and through which a second buffer solution flows; and partition walls fixed to communicating portions between the first and second flow passages with a predetermined bonding strength and configured to block movement of substances between the first and second flow passages. The partition walls are formed of a gel material having ion permeability.

Provided are a sample analysis method including separating albumin and ?-globulin from a sample containing albumin and ?-globulin, in an alkaline solution by capillary electrophoresis, in which the alkaline solution contains a cationic polymer, and the like.

When measuring electrophoretic mobility it is customary to apply an electric field and determine the electrophoretic velocity while minimizing all other contributions to the particle movement. A method and apparatus for the measurement of mobility while the sample is flowing is disclosed. Combined with a fractionation system, this approach further enables the direct measurement of individual species' mobility within a multi-modal sample. Other advantages of this new mobility measurement approach include the ability to easily pressurize the sample to suppress electrolysis, mitigation of oxidation-reduction effects and efficient heat dissipation.

A method for analyzing a component is provided. The method includes the steps of: (iii) providing the electrophoretic or thermophoretic movement of the component into a second fluid flow; (iv) diverting a part of a first fluid flow, a part of the second fluid flow, or parts of the first fluid flow and the second fluid flow, wherein the diverted part is a third fluid flow which includes, the component; (v) contacting the third fluid flow with a fourth fluid flow, such as to form a laminar flow; (vi) providing the diffusion of the component into the fourth fluid flows.

A determination method includes: using a microchip, including a capillary flow path and a sample reservoir connected to the capillary flow path at an upstream side, to fill the capillary flow path with a first solution for electrophoresis, and supply the sample reservoir with a second solution containing an analyte; applying a voltage between the sample reservoir supplied with the second solution and the inside of the capillary flow path filled with the first solution, to move a component contained in the second solution in the capillary flow path and separate the component in the capillary flow path; optically detecting a value related to a component difference between the first solution and the second solution, other than a value related to the analyte, for the separated component; and determining whether the optical detection is favorable or poor by comparing the optically detected value with a predetermined threshold value.

An automated method and system for identifying one or more chemical tracers present in a sample drawn downstream from the well head from a produced hydrocarbon oil/water stream in a pipeline from a downhole well completion, the one or more chemical tracers having originally been applied to the outer surface of one or more lengths of tubing placed at known locations in the assembly of the downhole well completion, the chemical identification of each of the tracers and the location of each of the tracers having been retrievably recorded for the well completion in the form of a relational database, by in situ testing of a portion of the aqueous layer of the sample following settling by means of an electrophoresis analysis system that includes a micro-fluidic chip and an electronic data information collection unit and signal communication means for transmitting conditioned data from the electronic data information collection unit to the central control station for comparison with, and identification of data associated with the chemical tracers and the location of the chemical tracers in the well completion from the relational database, and a user display device for displaying the results of the data comparison and identification so that appropriate remedial action to reduce the volume of produced water in the hydrocarbon stream can be taken.

The present analysis method for analyzing a sample uses capillary electrophoresis by applying a voltage to a sample solution introduced to a micro flow path, performing separation analysis for a component contained in the sample solution, and measuring an optical measurement value at a measurement section of the micro flow path corresponding to an elapsed time after a start of measurement. The analysis method comprises a waveform forming step of forming a waveform related to the optical measurement value corresponding to the elapsed time since the start of measurement; an interface detection step of determining an interface detection time based on the optical measurement value when an interface between the sample solution and a migration liquid reaches a predetermined measurement position in the micro flow path; a waveform feature specification step of specifying a plurality of waveform features appearing in the waveform; and a component identification step of identifying the component contained in the sample solution based on elapsed times corresponding to each of the waveform features as well as the interface detection time.

Various embodiments of the teachings relate to a system or method for sample preparation or analysis in biochemical or molecular biology procedures. The sample preparation can involve small volume processed in discrete portions or segments or slugs, herein referred to as discrete volumes. A molecular biology procedure can be nucleic acid analysis. Nucleic acid analysis can be an integrated DNA amplification/DNA sequencing procedure.

Disclosed herein are dielectrophoresis (DEP) devices having an alignment region, a DEP region, and an analysis region for characterizing particles. Disclosed herein are methods of characterizing particles, the methods include aligning particles along one or more walls of a microfluidic device, applying a non-uniform electric field to the particles, receiving the particles in a plurality of outlet channels, respectively, based on one or more electrical properties of the plurality of particles, passing at least one of the particles in one of the plurality of outlet channels through an impedance detector, and/or detecting an impedance measurement characteristic of at least one property of the at least one of the particles.

A micro-lab includes one or more electrophoresis devices each optically coupled to respective spectrometers and electronic signal processing, analysis and control, with fluids transported via a system of valves, tubes and pumps. The spectrograms are captured by a respective digital cameras, and chemical characteristics including molecular mobility, particle (molecular) charge, molecular weight, particle (molecular) pH, particle (molecular) dielectric, particle (molecular) conductivity, Raman spectrum of each chemical species, IR spectrum of particle (molecular) is determined, and principal component analysis is performed to identify and quantify chemical constituents.