Abstract:
A novel method of spatial compression of a DNA sample inside the capillary for the gel capillary electrophoresis and an article for operating the method are disclosed. In this method, after the electrokinetic injection, the sample is compressed using the reverse electric field. A special DNA barrier material is used to contain the sample in the capillary. We expect that this Electro Static Compression (ESC) can increase the DNA concentration in the capillary by orders of magnitude. In the proposed method and article the injection and compression of the DNA sample are followed by subsequent electrophoretic separation in any kind of sequencing container (for instance glass capillary). The use of the ESC method will allow the increase of the length and the quality of the read, as well as reduction of the DNA consumption. ESC method will also permit the use of low power illumination sources including miniature and inexpensive light emitting diodes (LED) instead of the Ar-ion laser for exciting fluorescent labels in 4-color DNA sequencing.
Abstract:
The present invention generally provides methods for enhancing transport and direction of materials in fluidic systems, which systems utilize electroosmotic (E/O) flow systems, to affect that transport and direction. The methods generally comprise providing an effective concentration of at least one zwitterionic compound in the fluid containing the material that is to be transported or directed.
Abstract:
A corrosion test cell for evaluating corrosion resistance in fuel cell bipolar plates is described. The cell has a transparent or translucent cell body having a pair of identical cell body members that seal against opposite sides of a bipolar plate. The cell includes an anode chamber and an cathode chamber, each on opposite sides of the plate. Each chamber contains a pair of mesh platinum current collectors and a catalyst layer pressed between current collectors and the plate. Each chamber is filled with an electrolyte solution that is replenished with fluid from a much larger electrolyte reservoir. The cell includes gas inlets to each chamber for hydrogen gas and air. As the gases flow into a chamber, they pass along the platinum mesh, through the catalyst layer, and to the bipolar plate. The gas exits the chamber through passageways that provide fluid communication between the anode and cathode chambers and the reservoir, and exits the test cell through an exit port in the reservoir. The flow of gas into the cell produces a constant flow of fresh electrolyte into each chamber. Openings in each cell body is member allow electrodes to enter the cell body and contact the electrolyte in the reservoir therein. During operation, while hydrogen gas is passed into one chamber and air into the other chamber, the cell resistance is measured, which is used to evaluate the corrosion properties of the bipolar plate.
Abstract:
Electrophoresis is performed simultaneously in a multitude of slab gels in a single cell that supports the slab gels vertically and parallel to each other while immersed in a buffer solution, and that applies a voltage to all gels simultaneously through a single pair of plate electrodes. Temperature control is achieved by circulating the buffer solution upward through the cell, entering near the base of each slab gel and leaving near the top, and cooling the circulating buffer solution with a tube heat exchanger positioned on the floor of the cell.
Abstract:
A microfluidic device has a layer with a capillary break formed by a capillary sluice. The capillary sluice has a lower surface and an upper surface. A first electrode is disposed on the lower surface. The first electrode is coupled to the voltage source. A second electrode spaced a predetermined distance from the first electrode is coupled to the voltage source. A controller may be used to control the voltage applied to the electrodes. The controller may alter the operation of the microfluidic chip in response to fluid sensed at the electrodes.
Abstract:
A microfluidic device has a layer that has a capillary break formed by a capillary sluice. The capillary sluice has a lower surface and an upper surface. An input channel is coupled to the capillary break. A first electrode is disposed proximate the lower surface. The first electrode is coupled to the voltage source. A second electrode is spaced a first predetermined distance from the first electrode coupled to the voltage source. A third electrode is spaced apart from the second electrode and positioned within the input channel from the first electrode coupled to the voltage source.
Abstract:
In a method for positioning or controlling the motion of an object in a multi-electrode arrangement for forming a field cage, the basic potentials for driving the electrodes are modulated with drive potentials in such a way that the object position in the field cage changes in relation to a predetermined position or path. A device for arranging objects at predetermined positions in a multi-electrode arrangement has a switching device by which basic potentials, produced by generator means, can be modulated according to predetermined drive potentials (FIG. 1).
Abstract:
The present invention provides methods of electrophoretically separating macromolecular species, as well as compositions and systems useful in carrying out such methods. Specifically, the methods of the present invention comprise providing a substrate that has at least a first capillary channel disposed therein. The surface of the channel has a first surface charge associated therewith, and is filled with a water soluble surface adsorbing polymer solution that bears a net charge that is the same as the charge on the capillary surface.
Abstract:
An emission control system for determining a concentration of oxygen in a flow of gas which has a sensor. The sensor has a diffusion barrier, an electrolyte material, and a counter-electrode. The counter-electrode is configured to support the diffusion barrier, and the electrolyte material is disposed between the diffusion barrier and the counter-electrode.
Abstract:
Devices and methods are disclosed for moving charged molecules through a medium by the application of a plurality of electrical fields of sufficient strength and applied for sufficient amounts of time so as to move the charged molecules through the medium. The devices although preferably small in size, preferably generate large numbers (100 or more) of electrical fields to a movement area which preferably contains a liquid buffered or gel medium. Mixtures of charged molecules are pulled through the gel by the force of the electrical fields. The fields are preferably activated simultaneously or sequentially one after another at various speeds to create complex force field distributions or moving field waves along the separation medium. Charged molecules capable of moving quickly through the gel will be moved along by the faster moving field waves and be separated from slower moving molecules. The fields can be activated by computer software and can be used to move molecules away from and toward each other to obtain rapid and complex chemical synthesis, sequencing or reaction protocols.