A system includes a housing, a cartridge retainer disposed within the housing, a detection assembly disposed within the housing, and a reagent tray holder movably disposed in the housing. The cartridge retainer configured to receive a capillary cartridge having a capillary. The detection assembly includes at least one emitter, a first detector, and a second detector. The detection assembly is configured to transition between a first configuration, in which the first detector detects a first output of the at least one emitter, and a second configuration, in which the second detector detects a second output of the at least one emitter. The reagent tray holder is configured to move relative to the cartridge retainer to place the capillary of the capillary cartridge in fluid communication with a reagent volume.

MCE assays and reagents to assess purity and to identify impurities in protein drug product samples are provided. Methods for analyzing analytes in a protein drug sample are provided.

Dual nucleic acid and protein isoform measurements are performed on low starting cell numbers (e.g. equivalent to the number of blastomeres composing early embryonic development stages (morula and blastocysts)), comprising integrating fractionation polyacrylamide gel electrophoresis (fPAGE) of 10-100 cells with off-chip analysis of nucleic acids in the nuclei.

Structures for improved electrophoretic precast gel substrates are disclosed herein. In some embodiments, an electrophoretic precast gel substrate includes a front plate comprising a first tenon-and-mortise connective structure, and a rear plate comprising a second tenon-and-mortise connective structure. The front plate and the rear plate can include snap features that are configured to provide a snap fit with a corresponding structure. The front and rear plates can be configured to be coupled and/or decoupled along the first and second tenon-and-mortise connective structures.

Disclosed is a device for impregnation using electrophoresis, which includes a chassis, a storing unit, a pipeline unit, an injection unit, a bearing tank, a first driver element and a second driver element, wherein the storing unit has several storage tanks storing the materials for impregnation. The pipeline unit has several pipelines connecting the storage tanks and the injection unit. The injection unit has a static mixing tube and an injector, so as to inject said materials for impregnation into the several slide sets located in the bearing tank. The first driver element drives the bearing tank to reciprocate transversely, and the second driver element drives the injection unit to shift up and down. The device can perform impregnation operations automatically, with quick operation and low operational difficulty level, while the prepared gel has high quality stability and yield.

An electrophoretic separation device includes an anode and a cathode, a porous scaffold material, and a liquid separation medium, wherein the separation medium is located inside the porous scaffold material, is in contact with the cathode and the anode, and has been applied to the porous scaffold material in form of a custom-made geometrical shape defining a migration path for a biomolecule-containing sample, wherein the sample is enclosed by the separation medium. A method for electrophoretic separation of biomolecules includes the electrophoretic separation device, a biomolecule-containing sample, wherein the sample is applied to the porous scaffold material prior to the application of the separation medium, or the sample is applied to the separation medium located inside the porous scaffold material, resulting in enclosure of the sample by the separation medium, and applying a voltage to the separation medium by means of the anode and the cathode leading to the migration of the biomolecules inside the separation medium.

An electrophoresis device has: a sample tray (112) on which there are placed a positive-electrode-side buffer solution container (103) containing a buffer solution and a phoresis medium container (102) containing a phoresis medium, and which is driven in a vertical direction and a horizontal direction; a thermostat oven unit (113) that holds a capillary array having a capillary head in which a plurality of capillaries are bundled in a single unit at one end thereof in a state where the capillary array being held in a state in which the capillary head protrudes downward, and that keeps the interior temperature constant; a solution-delivering mechanism (106) for delivering the phoresis medium in the phoresis medium container to the capillary array from the capillary head; and a power source for applying a voltage to both ends of the capillary array. Holes for insertion of the capillary head are provided in upper sections of the positive-electrode-side buffer solution container and the phoresis medium container. The thermostat oven unit is provided with a first lid member (207) that is positioned above the sample tray and seals the upper section of the positive-electrode-side buffer solution container while the phoresis medium is being delivered by the solution-delivering mechanism.

An electrophoresis gel with a gel buffer that includes a gel amine buffer, a primary gel ampholyte, and a conjugate gel ampholyte is disclosed herein. The conjugate gel ampholyte may be selected from threonine and serine.

The disclosure relates to methods of characterizing ampholyte compositions suitable for downstream applications such as capillary isoelectric focusing using liquid-chromatography-mass spectrometry.

The present disclosure provides methods of improving the resolution of labeled glycans in capillary electrophoresis techniques using a gel as a sieving matrix, by incorporating polyamines in the gel.