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    • 2. 发明授权
    • Methods to improve immunogenicity of antigens and specificity of antibodies
    • 提高抗原免疫原性和抗体特异性的方法
    • US06455047B1
    • 2002-09-24
    • US09156864
    • 1998-09-18
    • Judith FitzpatrickRegina Lenda
    • Judith FitzpatrickRegina Lenda
    • A61K39385
    • C07K16/16A61K39/385A61K47/646A61K2039/6081A61K2039/627C07K16/18
    • A method of improving specific immune responses to small immunogens, haptens, has been developed by changing the linkage between the hapten and carrier being used for immunization. High affinity antibodies to the hapten cotinine have been produced using this method. Antibodies to a glycated protein have also been developed, utilizing an immunogen which is composed of a glycated peptide mimic of the glycated peptide sequence which is the target epitope, wherein the peptide mimic is constructed to conformationally mimic the conformation of the peptide in the native protein, the peptide mimic contains no charged groups or other immunodominant group, and the peptide mimic is connected to a spacer sequence equivalent to a peptide spacer of between one and thirty amino acids in length, which serves to position the peptide epitope in a conformation that approximates its conformation in the native protein. In a further embodiment the peptide mimic and spacer are linked to a carrier molecule.
    • 已经通过改变用于免疫的半抗原和载体之间的连接来开发提高对小免疫原(haptens)的特异性免疫应答的方法。 使用该方法已经产生了对半抗原可替宁的高亲和力抗体。 还开发了利用由作为靶表位的糖基化肽序列的糖基化肽模拟物构成的免疫原的糖基化蛋白质的抗体,其中构建该肽模拟物以构象地模拟天然蛋白质中的肽的构象 ,肽模拟物不含有带电荷基团或其他免疫显性基团,并且肽模拟物连接到等同于长度为一至三十个氨基酸之间的肽间隔物的间隔序列,其用于将肽表位定位成近似的构象 其在天然蛋白质中的构象。 在另一个实施方案中,肽模拟物和间隔基连接到载体分子。
    • 5. 发明授权
    • Methods to improve immunogenicity of antigens and specificity of antibodies
    • 提高抗原免疫原性和抗体特异性的方法
    • US07303750B2
    • 2007-12-04
    • US10224758
    • 2002-08-21
    • Judith FitzpatrickRegina Lenda
    • Judith FitzpatrickRegina Lenda
    • A61K39/385
    • C07K16/16A61K39/385A61K47/646A61K2039/6081A61K2039/627C07K16/18
    • A method of improving specific immune response to small immunogens, haptens, has been developed by changing the linkage between the hapten and carrier being used for immunization. High affinity antibodies to cotinine have been produced using this method. Antibodies to a glycated protein have also been developed, utilizing an immunogen which is composed of a glycated peptide mimic of the glycated peptide sequence which is the target epitope, wherein the peptide mimic is constructed to conformationally mimic the conformation of the peptide in the native protein, the peptide mimic contains no charged groups or other immunodominant group, and is connected to a spacer sequence equivalent to a peptide spacer of between one and thirty amino acids in length, which serves to position the peptide epitope in a conformation that approximates its conformation in the native protein. In another embodiment, the peptide mimic and spacer are linked to a carrier molecule.
    • 通过改变用于免疫的半抗原和载体之间的连接,已经开发了提高对小免疫原(半抗原)的特异性免疫应答的方法。 使用该方法制备了可替宁的高亲和力抗体。 还开发了利用由作为靶表位的糖基化肽序列的糖基化肽模拟物构成的免疫原的糖基化蛋白质的抗体,其中构建该肽模拟物以构象地模拟天然蛋白质中的肽的构象 ,肽模拟物不含有带电荷基团或其他免疫显性基团,并且与长度为一至三十个氨基酸的肽间隔物相当的间隔序列连接,其用于将肽表位定位成近似其构象的构象 天然蛋白质。 在另一个实施方案中,肽模拟物和间隔基连接至载体分子。
    • 7. 发明授权
    • Methods to improve immunogenicity of antigens and specificity of antibodies
    • 提高抗原免疫原性和抗体特异性的方法
    • US07335516B2
    • 2008-02-26
    • US10224772
    • 2002-08-21
    • Judith FitzpatrickRegina Lenda
    • Judith FitzpatrickRegina Lenda
    • G01N33/531A61K38/03C07K17/02C07K16/44
    • C07K16/16A61K39/385A61K47/646A61K2039/6081A61K2039/627C07K16/18
    • A method of improving specific immune responses to small immunogens, haptens, has been developed by changing the linkage between the hapten and carrier being used for immunization. Antibodies to a glycated protein have been developed, utilizing an immunogen which is composed of a glycated peptide mimic of the glycated peptide sequence which is the target epitope, wherein the peptide mimic is constructed to conformationally mimic the conformation of the peptide in the native protein, the peptide mimic contains no charged groups or other immunodominant group, and the peptide mimic is connected to a spacer sequence equivalent to a peptide spacer of between one and thirty amino acids in length, which serves to position the peptide epitope in a conformation that approximates its conformation in the native protein. In a further embodiment the peptide mimic and spacer are linked to a carrier molecule.
    • 已经通过改变用于免疫的半抗原和载体之间的连接来开发提高对小免疫原(haptens)的特异性免疫应答的方法。 已经开发出抗糖基化蛋白质的抗体,利用由作为靶表位的糖基化肽序列的糖基化肽模拟物构成的免疫原,其中肽模拟物构建成构象地模拟天然蛋白质中肽的构象, 肽模拟物不含有带电荷基团或其他免疫显性基团,并且肽模拟物连接至长度为一至三十个氨基酸的等同于肽间隔基的间隔序列,其用于将肽表位置于近似于其的构象 天然蛋白质中的构象。 在另一个实施方案中,肽模拟物和间隔基连接到载体分子。