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    • 1. 发明申请
    • Method for quantifying phosphokinase activity on proteins
    • 蛋白质磷酸激酶活性定量的方法
    • US20090104628A1
    • 2009-04-23
    • US12179526
    • 2008-07-24
    • Kevin J. REAGANErik SchaeferJimin Wang
    • Kevin J. REAGANErik SchaeferJimin Wang
    • G01N33/573C07K16/40
    • C07K16/2863C07K16/18C07K2317/34C12Q1/485G01N2333/4709
    • The invention involves a method for measuring phosphorylation of proteins at specific sites and, as such, is an indicator of the protein kinase activity of enzymes capable of phosphorylating those sites. The method involves the in vitro or in vivo phosphorylation of a target protein at a specific serine, threonine or tyrosine residue, subjecting that protein (non-phosphorylated) to reaction mixture containing all reagents, including phosphokinase which allow the creation of a phosphorylated form of protein. The phosphorylated protein is measured by contacting it with an antibody specific for the phosphorylation site(s). The invention includes antibodies useful in practicing the methods of the invention. The invention particularly relates to all proteins modified by phosphorylation and dephosphorylation as illustrated by Tau, Rb and EGFR proteins and antibodies specific for the site of phosphorylation of the Tau, Rb or EGFR proteins.
    • 本发明涉及一种用于测量特定位点蛋白质磷酸化的方法,因此是能够使这些位点磷酸化的酶的蛋白激酶活性的指标。 该方法包括在特定丝氨酸,苏氨酸或酪氨酸残基处的靶蛋白的体外或体内磷酸化,使该蛋白质(非磷酸化)到含有所有试剂的反应混合物,包括磷酸激酶,其允许产生磷酸化形式 蛋白。 通过使磷酸化蛋白质与针对磷酸化位点特异的抗体接触来测量磷酸化蛋白质。 本发明包括可用于实践本发明方法的抗体。 本发明特别涉及通过磷酸化和去磷酸化修饰的所有蛋白质,如Tau,Rb和EGFR蛋白质所示,以及对Tau,Rb或EGFR蛋白质的磷酸化位点特异的抗体。
    • 3. 发明授权
    • Method for quantifying phosphokinase activity on proteins
    • 蛋白质磷酸激酶活性定量的方法
    • US08114617B2
    • 2012-02-14
    • US12970250
    • 2010-12-16
    • Kevin J. ReaganErik SchaeferJimin Wang
    • Kevin J. ReaganErik SchaeferJimin Wang
    • G01N33/53G01N33/543
    • C07K16/2863C07K16/18C07K2317/34C12Q1/485G01N2333/4709
    • The invention involves a method for measuring phosphorylation of proteins at specific sites and, as such, is an indicator of the protein kinase activity of enzymes capable of phosphorylating those sites. The method involves the in vitro or in vivo phosphorylation of a target protein at a specific serine, threonine or tyrosine residue, subjecting that protein (non-phosphorylated) to reaction mixture containing all reagents, including phosphokinase which allow the creation of a phosphorylated form of protein. The phosphorylated protein is measured by contacting it with an antibody specific for the phosphorylation site(s). The invention includes antibodies useful in practicing the methods of the invention. The invention particularly relates to all proteins modified by phosphorylation and dephosphorylation as illustrated by Tau, Rb and EGFR proteins and antibodies specific for the site of phosphorylation of the Tau, Rb or EGFR proteins.
    • 本发明涉及一种用于测量特定位点蛋白质磷酸化的方法,因此是能够使这些位点磷酸化的酶的蛋白激酶活性的指标。 该方法包括在特定丝氨酸,苏氨酸或酪氨酸残基处的靶蛋白的体外或体内磷酸化,使该蛋白质(非磷酸化)到含有所有试剂的反应混合物,包括磷酸激酶,其允许产生磷酸化形式 蛋白。 通过使磷酸化蛋白质与针对磷酸化位点特异性的抗体接触来测量磷酸化蛋白质。 本发明包括可用于实践本发明方法的抗体。 本发明特别涉及通过磷酸化和去磷酸化修饰的所有蛋白质,如Tau,Rb和EGFR蛋白质所示,以及对Tau,Rb或EGFR蛋白质的磷酸化位点特异的抗体。
    • 4. 发明申请
    • METHOD FOR QUANTIFYING PHOSPHOKINASE ACTIVITY ON PROTEINS
    • 蛋白质磷酸酶活性定量的方法
    • US20110165588A1
    • 2011-07-07
    • US12970250
    • 2010-12-16
    • Kevin J. ReaganErik SchaeferJimin Wang
    • Kevin J. ReaganErik SchaeferJimin Wang
    • G01N33/53
    • C07K16/2863C07K16/18C07K2317/34C12Q1/485G01N2333/4709
    • The invention involves a method for measuring phosphorylation of proteins at specific sites and, as such, is an indicator of the protein kinase activity of enzymes capable of phosphorylating those sites. The method involves the in vitro or in vivo phosphorylation of a target protein at a specific serine, threonine or tyrosine residue, subjecting that protein (non-phosphorylated) to reaction mixture containing all reagents, including phosphokinase which allow the creation of a phosphorylated form of protein. The phosphorylated protein is measured by contacting it with an antibody specific for the phosphorylation site(s). The invention includes antibodies useful in practicing the methods of the invention. The invention particularly relates to all proteins modified by phosphorylation and dephosphorylation as illustrated by Tau, Rb and EGFR proteins and antibodies specific for the site of phosphorylation of the Tau, Rb or EGFR proteins.
    • 本发明涉及一种用于测量特定位点蛋白质磷酸化的方法,因此是能够使这些位点磷酸化的酶的蛋白激酶活性的指标。 该方法包括在特定丝氨酸,苏氨酸或酪氨酸残基处的靶蛋白的体外或体内磷酸化,使该蛋白质(非磷酸化)到含有所有试剂的反应混合物,包括磷酸激酶,其允许产生磷酸化形式 蛋白。 通过使磷酸化蛋白质与针对磷酸化位点特异性的抗体接触来测量磷酸化蛋白质。 本发明包括可用于实践本发明方法的抗体。 本发明特别涉及通过磷酸化和去磷酸化修饰的所有蛋白质,如Tau,Rb和EGFR蛋白质所示,以及对Tau,Rb或EGFR蛋白质的磷酸化位点特异的抗体。
    • 5. 发明授权
    • Method for quantifying phosphokinase activity on proteins
    • 蛋白质磷酸激酶活性定量的方法
    • US07888050B2
    • 2011-02-15
    • US12179526
    • 2008-07-24
    • Kevin ReaganErik SchaeferJimin Wang
    • Kevin ReaganErik SchaeferJimin Wang
    • G01N33/53G01N33/543
    • C07K16/2863C07K16/18C07K2317/34C12Q1/485G01N2333/4709
    • The invention involves a method for measuring phosphorylation of proteins at specific sites and, as such, is an indicator of the protein kinase activity of enzymes capable of phosphorylating those sites. The method involves the in vitro or in vivo phosphorylation of a target protein at a specific serine, threonine or tyrosine residue, subjecting that protein (non-phosphorylated) to reaction mixture containing all reagents, including phosphokinase which allow the creation of a phosphorylated form of protein. The phosphorylated protein is measured by contacting it with an antibody specific for the phosphorylation site(s). The invention includes antibodies useful in practicing the methods of the invention. The invention particularly relates to all proteins modified by phosphorylation and dephosphorylation as illustrated by Tau, Rb and EGFR proteins and antibodies specific for the site of phosphorylation of the Tau, Rb or EGFR proteins.
    • 本发明涉及一种用于测量特定位点蛋白质磷酸化的方法,因此是能够使这些位点磷酸化的酶的蛋白激酶活性的指标。 该方法包括在特定丝氨酸,苏氨酸或酪氨酸残基处的靶蛋白的体外或体内磷酸化,使该蛋白质(非磷酸化)到含有所有试剂的反应混合物,包括磷酸激酶,其允许产生磷酸化形式 蛋白。 通过使磷酸化蛋白质与针对磷酸化位点特异性的抗体接触来测量磷酸化蛋白质。 本发明包括可用于实践本发明方法的抗体。 本发明特别涉及通过磷酸化和去磷酸化修饰的所有蛋白质,如Tau,Rb和EGFR蛋白质所示,以及对Tau,Rb或EGFR蛋白质的磷酸化位点特异的抗体。