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Francis J Lenoch

age ~67

from Madison, WI

Also known as:
  • Frank K Lenoch
  • Frank J Lenoch
Phone and address:
220 Bordner Dr, Madison, WI 53705
6082331483

Francis Lenoch Phones & Addresses

  • 220 Bordner Dr, Madison, WI 53705 • 6082331483
  • Fitchburg, WI
  • 220 Bordner Dr, Madison, WI 53705 • 6087519009

Work

  • Position:
    Educator

Education

  • Degree:
    Associate degree or higher

Emails

Us Patents

  • Process For Reverse Transcriptase Activity Measurement Using Fluorescence Polarization

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  • US Patent:
    61000396, Aug 8, 2000
  • Filed:
    Jan 28, 1999
  • Appl. No.:
    9/239355
  • Inventors:
    Thomas J. Burke - Madison WI
    Randall E. Bolger - Oregon WI
    Francis J. Lenoch - Madison WI
  • Assignee:
    Panvera, Inc. - Madison WI
  • International Classification:
    C12Q 168
    C07K 14005
    C07H 2104
  • US Classification:
    435 6
  • Abstract:
    Described is a process for detecting reverse transcriptase activity and, thereby, reverse transcriptase inhibitors using fluorescence polarization, comprising, mixing a DNA primer with an RNA template. Then forming an RNA/DNA duplex utilizing the reverse transcriptase and removing the RNA from the RNA/DNA duplex to form single-stranded DNA. Finally, adding a fluorescent-labeled oligonucleotide complementary to the single-stranded DNA for hybridizing to the single-stranded DNA; and, measuring the fluorescence polarization.
  • Method For Detecting And Quantitating Nucleic Acid Impurities In Biochemical Preparations

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  • US Patent:
    58245570, Oct 20, 1998
  • Filed:
    Apr 2, 1996
  • Appl. No.:
    8/626520
  • Inventors:
    Thomas J. Burke - Madison WI
    Randall E. Bolger - Oregon WI
    Francis J. Lenoch - Madison WI
  • Assignee:
    PanVera Corporation - Madison WI
  • International Classification:
    C12Q 168
    G01N 3348
  • US Classification:
    436 94
  • Abstract:
    A homogeneous fluorescence-based nucleic acid detection and quantitation system is provided to measure nucleic acid in protein solutions. The process relies on the intercalation of a non-fluorescent dye into a double-stranded nucleic acid helix or single-stranded nucleic acid. The dye fluoresces after intercalation and the intensity is a direct measurement of the amount of nucleic acid present in the sample.

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