U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Molecular biological diagnostic systems including electrodes

Patent 5632957 Issued on May 27, 1997. Estimated Expiration Date: Icon_subject September 9, 2014. 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

Semi-conductor non-volatile optical memory device
Patent #: 3950738
Issued on: 04/13/1976
Inventor: Hayashi ,   et al.

Mobile ion film memory
Patent #: 3995190
Issued on: 11/30/1976
Inventor: Salgo

Detection of microbial nucleic acids by a one-step sandwich hybridization test
Patent #: 4563419
Issued on: 01/07/1986
Inventor: Ranki ,   et al.

Sample-scanning photometer
Patent #: 4580895
Issued on: 04/08/1986
Inventor: Patel

Process and apparatus for electrically desorbing components selectively sorbed on an electrolytically conducting barrier
Patent #: 4584075
Issued on: 04/22/1986
Inventor: Goldstein ,   et al.

Process and apparatus for electrically desorbing components selectively sorbed on granules
Patent #: 4594135
Issued on: 06/10/1986
Inventor: Goldstein

Methods and kits for performing nucleic acid hybridization assays
Patent #: 4751177
Issued on: 06/14/1988
Inventor: Stabinsky

Method and means for annealing complementary nucleic acid molecules at an accelerated rate
Patent #: 4787963
Issued on: 11/29/1988
Inventor: MacConnell

Method and apparatus for performing automated, multi-sequential immunoassays
Patent #: 4816418
Issued on: 03/28/1989
Inventor: Mack ,   et al.

Silicon semiconductor wafer for analyzing micronic biological samples
Patent #: 4908112
Issued on: 03/13/1990
Inventor: Pace

More ...

Inventors

Application

No. 304657 filed on 09/09/1994

US Classes:

422/68.1, Means for analyzing liquid or solid sample257/E21.43, Recessing gate by adding semiconductor material at source (S) or drain (D) location, e.g., transist or with elevated single crystal S and D (EPO)257/E21.435, Lateral single gate single channel silicon transistor with both lightly doped source and drain extensions and source and drain self-aligned to sides of gate, e.g., LDD MOSFET, DDD MOSFET (EPO)257/E29.267, With nonplanar structure (e.g., gate or source or drain being nonplanar) (EPO)422/50, ANALYZER, STRUCTURED INDICATOR, OR MANIPULATIVE LABORATORY DEVICE422/52, Chemiluminescent422/55, Structured visual or optical indicator, per se422/56, Having reagent in absorbent or bibulous substrate422/61, Test package or kit422/62, Automatic analytical monitor and control of industrial process422/63, Sample mechanical transport means in or for automated analytical system422/67, With specific analytical program control means422/69, Sorption testing422/81, Automated system with sample fluid pressure transport means422/82.01, Measuring electrical property422/82.02, Resistance or conductivity422/82.03, Ion selective electrode422/82.04, Dissolved gas422/82.05, Measuring optical property by using ultraviolet, infrared, or visible light435/6, Involving nucleic acid435/7.1, Involving antigen-antibody binding, specific binding protein assay or specific ligand-receptor binding assay435/173.1, TREATMENT OF MICRO-ORGANISMS OR ENZYMES WITH ELECTRICAL OR WAVE ENERGY (E.G., MAGNETISM, SONIC WAVES, ETC.)436/501, BIOSPECIFIC LIGAND BINDING ASSAY536/22.1, N-glycosides, polymers thereof, metal derivatives (e.g., nucleic acids, oligonucleotides, etc.)536/23.1, DNA or RNA fragments or modified forms thereof (e.g., genes, etc.)536/24.1Non-coding sequences which control transcription or translation processes (e.g., promoters, operators, enhancers, ribosome binding sites, etc.)

Examiners

Primary: Marschel, Ardin H.

Attorney, Agent or Firm

Foreign Patent References

  • 0228075 EP. 07/13/1987
  • 2156074 GB. 10/13/1985
  • 2247889 GB. 03/13/1992
  • 86003782 WO. 07/13/1986
  • 8910977 WO. 11/13/1989
  • 9001564 WO. 02/13/1990
  • WO95/07363 WO. 03/13/1995
  • 57087 YU. 02/13/1987

International Classes

C12M 001/34
C12M 001/42
C12Q 001/68

Abstract

A system for performing molecular biological diagnosis, analysis and multi-step and multiplex reactions utilizes a self-addressable, self-assembling microelectronic system for actively carrying out controlled reactions in microscopic formats. These reactions include most molecular biological procedures, such as nucleic acid hybridization, antibody/antigen reaction, and clinical diagnostics. Multi-step combinatorial biopolymer synthesis may be performed. A controller interfaces with a user via input/output devices, preferably including a graphical display. Independent electronic control is achieved for the individual microlocations. In the preferred embodiment, the controller interfaces with a power supply and interface, the interface providing selective connection to the microlocations, polarity reversal, and optionally selective potential or current levels to individual electrodes. A system for performing sample preparation, hybridization and detection and data analysis integrates multiple steps within a combined system. Charged materials are transported preferably via free field electrophoresis. DNA complexity reduction is achieved preferably by binding of DNA to a support, followed by cleaving unbound materials, such as by restriction enzymes, followed by transport of the cleaved DNA fragments. Active, programmable matrix devices are formed in a variety of formats, including a square matrix pattern with fanned out electrical connections, an array having electrical connections and optionally optical connections from beneath the specific microlocations. A highly automated DNA diagnostic system results.

Other References

  • Anand and Southern, "Pulsed field gel electrophoresis," Gel Electrophoresis of Nucleic Acids--A Practical Approach, 2d edition, eds. D. Rickwood and B.D. Hames, (New York:IRL Press 1990) pp. 101-123
  • Anderson and Young, "Quantitative Filter Hybridisation," Nucleic Acid Hybridization--A Practical Approach, eds. B.D. Hames and S.J. Higgins (Washington DC:IRL Press 1985) pp. 73-111
  • Bains, "Setting a Sequence to Sequence a Sequence," Bio/Technology, 10:757-758 (1992)
  • Barinaga, "Will `DNA Chip` Speed Genome Initiative?" Science, 253:1489 (1991)
  • Beattie et al., "Genosensor Technology," The 1992 San Diego Conference: Genetic Recognition, pp. 1-5, (Nov., 1992)
  • Beltz et al., "Isolation of Multigene Families and Determination of Homologies by Filter Hybridization Methods," Methods in Enzymology, 100:266-285 (1983)
  • Connor et al., "Detection of sickle cell ଲs -globin allele by hybridization with synthetic oligonucleotides," Proc. Natl. Acad. Sci. USA, 80:278-282 (1983)
  • Drmanac et al., "Sequencing of Megabase Plus DNA by Hybridization: Theory of the Method," Genomics, 4:114-128 (1989)
  • Drmanac et al., "DNA Sequence Determination by Hybridization: A Strategy for Efficient Large-Scale Sequencing," Science, 260:1649-1652 (1993)
  • Fodor et al., "Multiplexed biochemical assays with biological chips," Nature, 364:555-556 (1993)
  • Fodor et al., "Light-Directed, Spatially Addressable Parallel Chemical Synthesis," Science, 251:767-773 (1991)
  • Horejsi, "Some Theoretical Aspects of Affinity Electrophoresis," Journal of Chromatography, 178:1-13 (1979)
  • Horejsi et al., "Determination of Dissociation Constants of Lectin Sugar Complexes by Means of Affinity Electrophoresis", Biochimica et biophysica acta, 499:290-300 (1977)
  • Ranki et al., "Sandwich hybridization as a convenient method for the detection of nucleic acids in crude samples," Gene, 21:77-85 (1983)
  • Saiki, "Amplification of Genomic DNA," PCR Protocols: A Guide to Methods and Applications, (Academic Press, Inc. 1990) pp. 13-20
  • Southern et al., "Analyzing and Comparing Nucleic Acid Sequences by Hybridization to Arrays of Oligonucleotides: Evaluation Using Experimental Models," Genomics, 13:1008-1017 (1992)
  • Strezoska et al., "DNA sequencing by hybridization: 100 bases read by a non-gel-based method," Proc. Natl. Acad. Sci. USA, 88:10089-10093 (1991)
  • Wallace et al., "Hybridization of synthetic oligodcoxyribonucleotides to .PHI.×174 DNA: the effect of single base pair mismatch," Nucleic Acid Res., 6:3543-3557 (1979)
  • Washizu, "Electrostatic manipulation of biological objects," Journal of Electrostatics, 25:109-123 (1990)
  • Washizu and Kurosawa, "Electrostatic Manipulation of DNA in Microfabricated Structures," IEEE Transactions on Industry Applications, 26:1165-1172 (1990
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