摘要:
The present invention relates generally to any application involving the monitoring of signal arising from ions produced by electrospray or other high pressure (>100 torr) ion sources. The present invention relates specifically to an apparatus and method for the detection of ions emitted from a capillary electrophoresis (CE) system, liquid chromatography, or other small-scale separation methods. And further, the invention provides a very simple diagnostic as to the quality of the separation and the operation of an electrospray source.
摘要:
Apparatus and methods are provided for increasing the sensitivity of detection of ionic species separated by capillary electrophoresis. The apparatus includes capillary electrophoretic separating means, suppressor means and detector means.
摘要:
Improved capillary electrophoresis apparatus of the type that generally includes a capillary tube, the capillary tube having a sample inlet end and an outlet end, a first electrode in electrical communication with the inlet end of the capillary tube, a second electrode in electrical communication with the outlet end of the capillary tube and a high voltage power supply in electrical communication with the first and second electrodes. The improvement is to connect a miniature Ion Chromatography membrane suppressor to the outlet end of the capillary tube, to connect a conductivity detector to the membrane suppressor and to place the second electrode in the regenerant compartment of the membrane suppressor. The method embodiment of the invention for anion analysis includes the steps of: (a) separating anions of interest by capillary electrophoresis in a buffer solution; (b) exchanging cations of the buffer for regenerant cations using an ion chromatography membrane suppressor to reduce the electrical conductivity of the buffer to produce a suppressed buffer; and (c) measuring the electrical conductivity of the suppressed buffer to determine the separated anions. Similarly, the method embodiment of the invention for cation analysis includes the steps of: (a) separating cations of interest by capillary electrophoresis in a buffer solution; (b) exchanging anions of the buffer for regenerant anions using a stationary means for exchanging anions thereby reducing the electrical conductivity of the buffer to produce a suppressed buffer; and (c) measuring the electrical conductivity of the suppressed buffer to determine the separated cations.
摘要:
This invention involves the elution of macromolecules such as proteins, deoxyribonucleic acid(DNA), ribonucleic acid(RNA) from solid phase matrix such as polyacrylamide, agarose and membranes such as polyvinyl difluoride (PVDF) in an electric field. The elution chamber shown in FIG. 1 consists of two separate screws 9, 9a and attachable chamber 1. The screw well 8 holds the gel matrix containing the macromolecules and is separated by the bottom chamber 1 with a membrane 5 with a nominal molecular weight cutoff higher than the macromolecule. On the other hand, the macromolecule is retained in the well 1 by introducing another membrane 6 having a molecular weight cutoff lower than the molecular weight of the macromolecule. Alternatively, macromolecules separated on membrane, e.g. PVDF, are held in a Teflon or plastic membrane holder 11. This holder can fit inside well 8 in screw 9. In addition, chamber 1 contains a well 7. The macromolecules migrate through the electrophoretic field and are concentrated in well 7. Since the volume of the well 7 is predetermined (10 ul--one ml or more), results in concentration of the macromolecules. Next, the chamber 1 is unscrewed from the top screw 8 and closed with a screw without a hole 13, and the entire device is submerged into a dialysis buffer. Following dialysis for a given time, the fluid above the bottom screw 9a itself and the membrane beneath it are removed. The sample is taken out from hole 7. If further concentration of the sample is required, then following removal of the fluid above the screw 9a, the entire device is transferred to a vacuum desiccator and concentrated to any desired volume.
摘要:
An introduction means for the direct introduction of a sample taken from a planar electrophoresis into an interface to a mass spectrometer utilizing laser desorption ionization. The introduction means includes a probe to collect a sample from a planar electrophoresis, generally a gel electrophoresis, comprising a dual electrode assembly and a potential gradient between the electrodes to collect the sample. Alternatively, the sample is obtained from a freeze-squeeze method or a drying/matrix-deposition method.
摘要:
A multiple electrophoresis method and device are disclosed for the controlled migration of macromolecules in gel plates stacked in a direction perpendicular to their plane, at least one series of electrodes (20) disposed at the intersections of two series of peripendicular planes, some perpendicular to the plates (12) and to the desired direction of migration of the macromolecules, the others perpendicular to the first and parallel to the plates (12), the electrodes being connected together selectively and controlled so as to provide both separation of the macromolecules in the plate (12) then transfer thereof to the membranes (22) associated with the plates (12).
摘要:
An electroelutor provides electroelution and concentration of small amounts of proteins from sample gels. The electroelutor elutes desired molecules from gels in a sample holder directly onto a membrane of a centrifuge concentrator or a sequencing membrane. After electroelution, the eluted molecules can be concentrated or processed in a sequencing device with minimized sample handling and minimized disturbance abouFUNDINGWork described herein relating to the present invention has been funded under contract no. DK35 306 awarded by the National Institutes of Health.
摘要:
A method and apparatus for use in biological testing. The apparatus comprises electrophoresis apparatus comprising a tank (1) the interior of which is formed with a raised portion (5) which splits the tank into the two compartments (6,7) containing electrophoresis electrolyte. Electrodes (8) are provided in each compartment. Electrophoresis is carried out through a gel (not shown) supported by a rigid porous plate (11). The gel is cast onto the porous plate with a transfer membrane (not shown) between the porous plate and the gel. Further electrodes (20,21) are mounted below and above the gel respectively. The method of the invention comprises a first stage using the electric field produced by the electrodes (8) to draw the samples through the gel and a second stage using the electric field produced by the electrodes (20,21) to draw the distributed macromolecules onto the transfer membrane.
摘要:
In an electro-elution apparatus for operation in an electrophoresis chamber and for the electro-elution of biological macromolecules from sections of electrophoresis gel, the macromolecules which are to be eluted are not temporarily adsorbed in a gel, but can be collected between two polymer membranes in a trap and pipetted out of the latter. The membrane, which is the first or inner membrane in the direction of migration of the macromolecules, is here permeable to the macromolecules under the action of the electric field, while the membrane, which is the second membrane in the direction of migration, namely the outer membrane of the electro-elution apparatus, is impermeable to the macromolecules under the same conditions. After the electric field has been switched off, both membranes are at least substantially impermeable to any mass transfer.