The Experts below are selected from a list of 51 Experts worldwide ranked by ideXlab platform

亮二 阿部 - One of the best experts on this subject based on the ideXlab platform.

  • antibody subjected to fluorescent labeling using nucleotide binding site nbs of antibody
    2016
    Co-Authors: 上田 宏, 熙陳 鄭, 金華 董, 亮二 阿部
    Abstract:

    Provided are: a method for using a nucleotide binding site present in the variable domain of the antibody to prepare, through a photochemical modification method, a fluorescent labeled antibody in which the fluorescence intensity changes with the binding of an antigen; and a fluorescent labeled antibody obtained thereby. A labeled antibody for fluoroimmunoassay in which a compound for labeling a nucleotide binding site (NBS) of the antibody and having indole butyric acid (IBA) and a fluorescent Group bound thereto is conjugated to a nucleotide binding site in the antibody. The compound is represented by formula (1) (in the formula, F is a fluorescent Group, and R is a linking Group selected from the Group consisting of an alkyl Group, alkenyl Group, alkynyl Group, C4–C10 cycloalkyl Group, C4–C10 heterocyclyl Group, C4–C10 aryl Group, C4–C10 Heteroaryl Group, arylene Group, ether Group, ester Group, PEG Group, sulfide Group, amide Group, ketone Group, and sulfamide Group, the Groups being substituted or unsubstituted, and combinations thereof).

  • antibody subjected to fluorescent labeling using nucleotide binding site nbs of antibody
    2016
    Co-Authors: 上田 宏, 熙陳 鄭, 金華 董, 亮二 阿部
    Abstract:

    Provided are: a method for using a nucleotide binding site present in the variable domain of the antibody to prepare, through a photochemical modification method, a fluorescent labeled antibody in which the fluorescence intensity changes with the binding of an antigen; and a fluorescent labeled antibody obtained thereby. A labeled antibody for fluoroimmunoassay in which a compound for labeling a nucleotide binding site (NBS) of the antibody and having indole butyric acid (IBA) and a fluorescent Group bound thereto is conjugated to a nucleotide binding site in the antibody. The compound is represented by formula (1) (in the formula, F is a fluorescent Group, and R is a linking Group selected from the Group consisting of an alkyl Group, alkenyl Group, alkynyl Group, C4–C10 cycloalkyl Group, C4–C10 heterocyclyl Group, C4–C10 aryl Group, C4–C10 Heteroaryl Group, arylene Group, ether Group, ester Group, PEG Group, sulfide Group, amide Group, ketone Group, and sulfamide Group, the Groups being substituted or unsubstituted, and combinations thereof).

J Suwinski - One of the best experts on this subject based on the ideXlab platform.

  • influence of Heteroaryl Group on electrochemical and spectroscopic properties of conjugated polymers
    Electrochimica Acta, 2012
    Co-Authors: Przemyslaw Data, Mieczyslaw Lapkowski, Radoslaw Motyka, J Suwinski
    Abstract:

    During our search for novel conjugated compounds, novel monomers and their polymers with selenophene and tellurophene Group were synthesized and characterized. Conjugated poly(p-phenylenevinylenes)s (PPV) derivatives attracted a large attention due to their photolouminescence properties. The stereocontrolled synthesis of 1,4-bis(2-(heteroar-2-yl) ethenyl)benzenes and 1,4-bis(heteroar-2-yl)benzenes with tellurophene, selenophene, thiophene and furan-based monomers has been successfully performed. Eight of p-phenylene derivatives have been synthesized, electrochemically polymerized and characterized.

上田 宏 - One of the best experts on this subject based on the ideXlab platform.

  • antibody subjected to fluorescent labeling using nucleotide binding site nbs of antibody
    2016
    Co-Authors: 上田 宏, 熙陳 鄭, 金華 董, 亮二 阿部
    Abstract:

    Provided are: a method for using a nucleotide binding site present in the variable domain of the antibody to prepare, through a photochemical modification method, a fluorescent labeled antibody in which the fluorescence intensity changes with the binding of an antigen; and a fluorescent labeled antibody obtained thereby. A labeled antibody for fluoroimmunoassay in which a compound for labeling a nucleotide binding site (NBS) of the antibody and having indole butyric acid (IBA) and a fluorescent Group bound thereto is conjugated to a nucleotide binding site in the antibody. The compound is represented by formula (1) (in the formula, F is a fluorescent Group, and R is a linking Group selected from the Group consisting of an alkyl Group, alkenyl Group, alkynyl Group, C4–C10 cycloalkyl Group, C4–C10 heterocyclyl Group, C4–C10 aryl Group, C4–C10 Heteroaryl Group, arylene Group, ether Group, ester Group, PEG Group, sulfide Group, amide Group, ketone Group, and sulfamide Group, the Groups being substituted or unsubstituted, and combinations thereof).

  • antibody subjected to fluorescent labeling using nucleotide binding site nbs of antibody
    2016
    Co-Authors: 上田 宏, 熙陳 鄭, 金華 董, 亮二 阿部
    Abstract:

    Provided are: a method for using a nucleotide binding site present in the variable domain of the antibody to prepare, through a photochemical modification method, a fluorescent labeled antibody in which the fluorescence intensity changes with the binding of an antigen; and a fluorescent labeled antibody obtained thereby. A labeled antibody for fluoroimmunoassay in which a compound for labeling a nucleotide binding site (NBS) of the antibody and having indole butyric acid (IBA) and a fluorescent Group bound thereto is conjugated to a nucleotide binding site in the antibody. The compound is represented by formula (1) (in the formula, F is a fluorescent Group, and R is a linking Group selected from the Group consisting of an alkyl Group, alkenyl Group, alkynyl Group, C4–C10 cycloalkyl Group, C4–C10 heterocyclyl Group, C4–C10 aryl Group, C4–C10 Heteroaryl Group, arylene Group, ether Group, ester Group, PEG Group, sulfide Group, amide Group, ketone Group, and sulfamide Group, the Groups being substituted or unsubstituted, and combinations thereof).

Przemyslaw Data - One of the best experts on this subject based on the ideXlab platform.

  • influence of Heteroaryl Group on electrochemical and spectroscopic properties of conjugated polymers
    Electrochimica Acta, 2012
    Co-Authors: Przemyslaw Data, Mieczyslaw Lapkowski, Radoslaw Motyka, J Suwinski
    Abstract:

    During our search for novel conjugated compounds, novel monomers and their polymers with selenophene and tellurophene Group were synthesized and characterized. Conjugated poly(p-phenylenevinylenes)s (PPV) derivatives attracted a large attention due to their photolouminescence properties. The stereocontrolled synthesis of 1,4-bis(2-(heteroar-2-yl) ethenyl)benzenes and 1,4-bis(heteroar-2-yl)benzenes with tellurophene, selenophene, thiophene and furan-based monomers has been successfully performed. Eight of p-phenylene derivatives have been synthesized, electrochemically polymerized and characterized.

金華 董 - One of the best experts on this subject based on the ideXlab platform.

  • antibody subjected to fluorescent labeling using nucleotide binding site nbs of antibody
    2016
    Co-Authors: 上田 宏, 熙陳 鄭, 金華 董, 亮二 阿部
    Abstract:

    Provided are: a method for using a nucleotide binding site present in the variable domain of the antibody to prepare, through a photochemical modification method, a fluorescent labeled antibody in which the fluorescence intensity changes with the binding of an antigen; and a fluorescent labeled antibody obtained thereby. A labeled antibody for fluoroimmunoassay in which a compound for labeling a nucleotide binding site (NBS) of the antibody and having indole butyric acid (IBA) and a fluorescent Group bound thereto is conjugated to a nucleotide binding site in the antibody. The compound is represented by formula (1) (in the formula, F is a fluorescent Group, and R is a linking Group selected from the Group consisting of an alkyl Group, alkenyl Group, alkynyl Group, C4–C10 cycloalkyl Group, C4–C10 heterocyclyl Group, C4–C10 aryl Group, C4–C10 Heteroaryl Group, arylene Group, ether Group, ester Group, PEG Group, sulfide Group, amide Group, ketone Group, and sulfamide Group, the Groups being substituted or unsubstituted, and combinations thereof).

  • antibody subjected to fluorescent labeling using nucleotide binding site nbs of antibody
    2016
    Co-Authors: 上田 宏, 熙陳 鄭, 金華 董, 亮二 阿部
    Abstract:

    Provided are: a method for using a nucleotide binding site present in the variable domain of the antibody to prepare, through a photochemical modification method, a fluorescent labeled antibody in which the fluorescence intensity changes with the binding of an antigen; and a fluorescent labeled antibody obtained thereby. A labeled antibody for fluoroimmunoassay in which a compound for labeling a nucleotide binding site (NBS) of the antibody and having indole butyric acid (IBA) and a fluorescent Group bound thereto is conjugated to a nucleotide binding site in the antibody. The compound is represented by formula (1) (in the formula, F is a fluorescent Group, and R is a linking Group selected from the Group consisting of an alkyl Group, alkenyl Group, alkynyl Group, C4–C10 cycloalkyl Group, C4–C10 heterocyclyl Group, C4–C10 aryl Group, C4–C10 Heteroaryl Group, arylene Group, ether Group, ester Group, PEG Group, sulfide Group, amide Group, ketone Group, and sulfamide Group, the Groups being substituted or unsubstituted, and combinations thereof).