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Aleksey V Rukavishnikov

age ~61

from Eugene, OR

Also known as:
  • Rukavishnikov Aleksey
Phone and address:
586 Brookside Dr, Eugene, OR 97405
5413422903

Aleksey Rukavishnikov Phones & Addresses

  • 586 Brookside Dr, Eugene, OR 97405 • 5413422903
  • 2555 Portland St, Eugene, OR 97405

Work

  • Company:
    Life technologies
  • Position:
    Senior staff scientist at life technologies

Education

  • Degree:
    Graduate or professional degree

Skills

Genomics • Lifesciences • Polymers • Biochemistry • Assay Development • Molecular Biology • Qpcr • Dna Sequencing • Pcr • Biotechnology • Protein Chemistry • Drug Discovery • Sequencing • Dna • High Throughput Screening

Industries

Biotechnology

Resumes

Aleksey Rukavishnikov Photo 1

Senior Staff Scientist At Life Technologies

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Location:
36 east 41St Pl, San Mateo, CA 94403
Industry:
Biotechnology
Work:
Life Technologies
Senior Staff Scientist at Life Technologies
Skills:
Genomics
Lifesciences
Polymers
Biochemistry
Assay Development
Molecular Biology
Qpcr
Dna Sequencing
Pcr
Biotechnology
Protein Chemistry
Drug Discovery
Sequencing
Dna
High Throughput Screening

Us Patents

  • Optically-Detectable Enzyme Substrates And Their Method Of Use

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  • US Patent:
    8318450, Nov 27, 2012
  • Filed:
    Jun 22, 2011
  • Appl. No.:
    13/166627
  • Inventors:
    Schuyler Corry - Eugene OR, US
    William Downey - Eugene OR, US
    Brian Filanoski - Spokane Valley WA, US
    Kyle Gee - Springfield OR, US
    Lawrence Greenfield - Eugene OR, US
    James Hirsch - Springfield OR, US
    Iain Johnson - Eugene OR, US
    Aleksey Rukavishnikov - Eugene OR, US
  • Assignee:
    Life Technologies Corporation - Carlsbad CA
  • International Classification:
    C12Q 1/34
  • US Classification:
    435 18, 435227, 435231
  • Abstract:
    The present invention relates to compounds that are substrates for an enzyme, and upon reaction with the enzyme provide a detectable response, such as an optically detectable response. In particular, the compounds have utility in detecting the presence of a β-lactamase in a sample. In addition to the compounds, methods are disclosed for analyzing a sample for the presence of a β-lactmase, for example, as an indicator of expression of a nucleic acid sequence including a sequence coding for a β-lactmase. Kits are disclosed that include the disclosed compounds and additional components, for example, cells, antibodies, a β-lactmase or instructions for using the components in an assay.
  • Labeling Reagents And Methods Of Their Use

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  • US Patent:
    8586743, Nov 19, 2013
  • Filed:
    Jan 30, 2008
  • Appl. No.:
    12/023019
  • Inventors:
    Kyle Gee - Springfield OR, US
    Aleksey Rukavishnikov - Eugene OR, US
    Diane M. Witczak - Williamsville NY, US
  • Assignee:
    Life Technologies Corporation - Carlsbad CA
  • International Classification:
    C07D 311/88
    C07D 307/00
    C07D 211/18
    C07D 277/62
    C07F 5/02
  • US Classification:
    546 13, 546 22, 546 58, 548110, 548156, 548157, 549226, 549302, 549303, 549304, 549467, 549470, 549471
  • Abstract:
    The present disclosure is directed to a reactive ester agent capable of conjugating a reporter molecule to a carrier molecule or solid support. The reactive ester agent has the general formula:.
  • Optically-Detectable Enzyme Substrates And Their Method Of Use

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  • US Patent:
    20050227309, Oct 13, 2005
  • Filed:
    Jan 21, 2005
  • Appl. No.:
    11/040924
  • Inventors:
    Schuyler Corry - Eugene OR, US
    William Downey - Eugene OR, US
    Brian Filanoski - Eugene OR, US
    Kyle Gee - Springfield OR, US
    I. Greenfield - Eugene OR, US
    James Hirsch - Springfield OR, US
    Iain Johnson - Eugene OR, US
    Aleksey Rukavishnikov - Eugene OR, US
  • International Classification:
    C12Q001/18
    C07D501/14
    C07D487/08
    C07F005/02
  • US Classification:
    435032000, 540222000, 540347000, 534726000, 534740000
  • Abstract:
    The present invention relates to compounds that are substrates for an enzyme, and upon reaction with the enzyme provide a detectable response, such as an optically detectable response. In particular, the compounds have utility in detecting the presence of a β-lactamase in a sample. In addition to the compounds, methods are disclosed for analyzing a sample for the presence of a β-lactmase, for example, as an indicator of expression of a nucleic acid sequence including a sequence coding for a β-lactmase. Kits are disclosed that include the disclosed compounds and additional components, for example, cells, antibodies, a β-lactmase or instructions for using the components in an assay.
  • Site-Specific Labeling Of Affinity Tags In Fusion Proteins

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  • US Patent:
    20050233307, Oct 20, 2005
  • Filed:
    Sep 12, 2003
  • Appl. No.:
    10/661451
  • Inventors:
    Kyle Gee - Springfield OR, US
    Courtenay Hart - Eugene OR, US
    Wai-Yee Leung - Eugene OR, US
    Wayne Patton - Eugene OR, US
    Aleksey Rukavishnikov - Eugene OR, US
    Richard Haugland - Eugene OR, US
    Zhenjun Diwu - Sunnyvale CA, US
  • International Classification:
    C12Q001/00
    G01N033/00
  • US Classification:
    435004000, 436086000
  • Abstract:
    The present invention provides methods and fluorescent compounds that facilitate detecting and labeling of a fusion protein by being capable of selectively binding to an affinity tag. The fluorescent compounds have the general formula A(B)n, wherein A is a fluorophore, B is a binding domain that is a charged chemical moiety, a protein or fragment thereof and n is an integer from 1-6 with the proviso that the protein or fragment thereof not be an antibody or generated from an antibody. The present invention provides specific fluorescent compounds and methods used to detect and label fusion proteins that contain a poly-histidine affinity tag. These compounds have the general formula A(L)m(B)n wherein A is a fluorophore, L is a linker, B is an acetic acid binding domain, m is an integer from 1 to 4 and n is an integer from 1 to 6. The acetic acid groups interact directly with the positively charged histidine residues of the affinity tag to effectively label and detect a fusion protein containing such an affinity tag when present in an acidic or neutral environment.
  • Fluorogenic Ph Sensitive Dyes And Their Method Of Use

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  • US Patent:
    20080274907, Nov 6, 2008
  • Filed:
    Oct 29, 2007
  • Appl. No.:
    11/927588
  • Inventors:
    Daniel Beacham - Eugene OR, US
    Jeffrey Dzubay - Eugene OR, US
    Kyle Gee - Springfield OR, US
    Vladimir Martin - Eugene OR, US
    Aleksey Rukavishnikov - Eugene OR, US
  • Assignee:
    INVITROGEN CORPORATION - Carlsbad CA
  • International Classification:
    C07D 455/04
    C07D 311/82
    C07D 209/12
    C40B 30/00
    G01N 33/68
    G01N 21/00
    C12Q 1/02
    C07F 5/02
    C07D 413/10
  • US Classification:
    506 7, 549390, 548525, 546138, 548490, 548405, 436172, 435 29, 436 86, 436 94
  • Abstract:
    A new class of pH sensitive fluorescent dyes and assays relating thereto are described. The dyes and assays are particularly suited for biological applications including phagocytosis and monitoring intracellular processes. The pH sensitive fluorescent dyes of the present invention include compounds of Formula I:
  • Optically-Detectable Enzyme Substrates And Their Method Of Use

    view source
  • US Patent:
    20090047692, Feb 19, 2009
  • Filed:
    Apr 7, 2008
  • Appl. No.:
    12/099085
  • Inventors:
    Schuyler Boon CORRY - Eugene OR, US
    William Louis Downey - Eugene OR, US
    Brian Filanoski - Spokane Valley WA, US
    Kyle Richard Gee - Springfield OR, US
    I. Lawrence Greenfield - Eugene OR, US
    James David Hirsch - Springfield OR, US
    Iain Johnson - Eugene OR, US
    Aleksey Rukavishnikov - Eugene OR, US
  • Assignee:
    INVITROGEN CORPORATION - Carlsbad CA
  • International Classification:
    G01N 33/53
    C07D 501/60
    C07D 498/04
    C12Q 1/34
  • US Classification:
    435 772, 540222, 540225, 540300, 435 18
  • Abstract:
    The present invention relates to compounds that are substrates for an enzyme, and upon reaction with the enzyme provide a detectable response, such as an optically detectable response. In particular, the compounds have utility in detecting the presence of a β-lactamase in a sample. In addition to the compounds, methods are disclosed for analyzing a sample for the presence of a β-lactmase, for example, as an indicator of expression of a nucleic acid sequence including a sequence coding for a β-lactmase. Kits are disclosed that include the disclosed compounds and additional components, for example, cells, antibodies, a β-lactmase or instructions for using the components in an assay.
  • Site-Specific Labeling Of Affinity Tags In Fusion Proteins

    view source
  • US Patent:
    20090081722, Mar 26, 2009
  • Filed:
    May 8, 2008
  • Appl. No.:
    12/117689
  • Inventors:
    Kyle Gee - Springfield OR, US
    Courtenay Hart - Eugene OR, US
    Wai-Yee Leung - San Ramon CA, US
    Wayne Patton - Newton MA, US
    Aleksey Rukavishnikov - Eugene OR, US
    Richard Haugland - Olympia WA, US
    Zhenjun Diwu - Okemos MI, US
  • Assignee:
    INVITROGEN CORPORATION - Carlsbad CA
  • International Classification:
    G01N 1/30
    C07F 5/02
    C07D 311/06
  • US Classification:
    435 405, 548405, 549289, 549283
  • Abstract:
    The present invention provides methods and fluorescent compounds that facilitate detecting and labeling of a fusion protein by being capable of selectively binding to an affinity tag. The fluorescent compounds have the general formula A(B)n, wherein A is a fluorophore, B is a binding domain that is a charged chemical moiety, a protein or fragment thereof and n is an integer from 1-6 with the proviso that the protein or fragment thereof not be an antibody or generated from an antibody. The present invention provides specific fluorescent compounds and methods used to detect and label fusion proteins that contain a poly-histidine affinity tag. These compounds have the general formula A(L)m(B)n wherein A is a fluorophore, L is a linker, B is an acetic acid binding domain, m is an integer from 1 to 4 and n is an integer from 1 to 6. The acetic acid groups interact directly with the positively charged histidine residues of the affinity tag to effectively label and detect a fusion protein containing such an affinity tag when present in an acidic or neutral environment.
  • Site-Specific Labeling Of Affinity Tags In Fusion Proteins

    view source
  • US Patent:
    20120270757, Oct 25, 2012
  • Filed:
    Mar 26, 2012
  • Appl. No.:
    13/429972
  • Inventors:
    Kyle GEE - Springfield OR, US
    Courtenay Hart - Eugene OR, US
    Wai-Yee Leung - San Ramon CA, US
    Wayne Patton - Newton MA, US
    Aleksey Rukavishnikov - Eugene OR, US
    Richard Haugland - Olympia WA, US
    Zhenjun Diwu - Okemos MI, US
  • Assignee:
    LIFE TECHNOLOGIES CORPORATION - Carlsbad CA
  • International Classification:
    G01N 21/76
    C07F 5/02
    C40B 70/00
    C07D 311/18
  • US Classification:
    506 41, 549288, 548405, 436 86
  • Abstract:
    The present invention provides methods and fluorescent compounds that facilitate detecting and labeling of a fusion protein by being capable of selectively binding to an affinity tag. The fluorescent compounds have the general formula A(B)n, wherein A is a fluorophore, B is a binding domain that is a charged chemical moiety, a protein or fragment thereof and n is an integer from 1-6 with the proviso that the protein or fragment thereof not be an antibody or generated from an antibody. The present invention provides specific fluorescent compounds and methods used to detect and label fusion proteins that contain a poly-histidine affinity tag. These compounds have the general formula A(L)m(B)n wherein A is a fluorophore, L is a linker, B is an acetic acid binding domain, m is an integer from 1 to 4 and n is an integer from 1 to 6.

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Aleksey Rukavishnikov

Youtube

My Broadcast

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Trip to Death Valley

Our March trip to Death Valley.

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Fort Rock

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