U.S. patents available from 1976 to present.
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Concentration of biological samples on a microliter scale and analysis by capillary electrophoresis

Patent 5766435 Issued on June 16, 1998. Estimated Expiration Date: Icon_subject March 22, 2016. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

3720593

Capillary electrophoretic device employing structure permitting electrical contact through ionic movement
Patent #: 4908116
Issued on: 03/13/1990
Inventor: Zare, et al.

Column separation system for electrophoresis with sample pretreatment
Patent #: 5085756
Issued on: 02/04/1992
Inventor: Swedberg

Field amplified polarity switching sample injection in capillary zone electrophoresis
Patent #: 5089099
Issued on: 02/18/1992
Inventor: Chien, et al.

Use of zwitterions to mobilize isoelectrically focused ampholyte zones
Patent #: 5110434
Issued on: 05/05/1992
Inventor: Zhu, et al.

System and method for improving sample concentration in capillary electrophoresis
Patent #: 5116471
Issued on: 05/26/1992
Inventor: Chien, et al.

Ion-permeable polymer joint for use in capillary electrophoresis
Patent #: 5169510
Issued on: 12/08/1992
Inventor: Lunte, et al.

On-column preconcentration of samples in capillary electrophoresis
Patent #: 5340452
Issued on: 08/23/1994
Inventor: Brenner, et al.

Process for effecting capillary electrophoresis Patent #: 5348658
Issued on: 09/20/1994
Inventor: Fuchs, et al.

Inventors

Assignee

Application

No. 620649 filed on 03/22/1996

US Classes:

204/451, Capillary electrophoresis204/453, With injection204/601, Capillary electrophoresis type204/604With injector

Examiners

Primary: Gorgos, Kathryn
Assistant: Starsiak, John S. Jr.

Attorney, Agent or Firm

International Classes

G01N 027/26
G01N 027/447

Abstract

The present invention provides new methods for the concentration of ionic solutes, particularly ampholytes, such as, for example, peptides, proteins and nucleic acids. The methods are based on the fact that the electrophoretic migration velocities of solutes decrease upon a decrease in the absolute value of the zeta-potential of a solute or the pore size of the electrophoresis medium, and upon an increase in the cross-section of the electrophoresis chamber, the viscosity of the electrophoresis medium, or the electrical conductivity of the electrophoresis medium. When applied to capillary electrophoresis, the methods described herein permit concentration of a solution of solutes in the same capillary tube as is used for the electrophoretic analysis. Alternatively, however, the sample can be withdrawn from the capillary tube following concentration of the solution of solutes and processed by techniques other than high-performance capillary electrophoresis (HPCE).

Other References

  • Andrews, Electrophoresis: Theory, Techniques, and Biochemical and Clinical Applications, 2nd ed., Clarendon Press, Oxford, pp. 254-255, 256, 278 and 299
  • Svensson, H., Acta Chemica Scandinavica, 16:456-466 (1962), no month availabl
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