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    • 82. 发明申请
    • Prostate-specific membrane antigen
    • 前列腺特异性膜抗原
    • US20070148662A1
    • 2007-06-28
    • US11480319
    • 2006-06-30
    • Ron IsraeliWarren HestonWilliam Fair
    • Ron IsraeliWarren HestonWilliam Fair
    • C12Q1/68G01N33/574C07H21/04C12P21/06C07K14/705
    • C07K14/4748A61K39/00C07K14/705C12Q1/6883C12Q2600/158G01N2800/342
    • This invention provides an isolated mammalian nucleic acid molecule encoding a mammalian prostate-specific membrane antigen. This invention also provides prostate-specific membrane nucleic acid of at least 15 nucleotides capable of specifically hybridizing with a sequence of a nucleic acid molecule encoding a mammalian prostate-specific membrane antigen. This invention further provides vector and vector host expression system for the prostate-specific membrane antigen. This invention also provides methods to identify ligands which bind to the prostate-specific membrane antigen, to generate antibody against a complete prostate-specific membrane antigen or a portion of the antigen. This invention further provides purified prostate-specific membrane antigen. This invention provides a therapeutic agent comprising an antibody directed against to prostate-specific membrane antigen and a cytotoxic agent conjugated thereto. This invention also provides a method of imaging prostate cancer and an immunoassay for measuring the amount of the prostate-specific membrane antigen in a biological simple. This invention further provides transgenic nonhuman mammal which comprises the isolated nucleic acid molecule encoding a mammalian prostate-specific membrane antigen.
    • 本发明提供了编码哺乳动物前列腺特异性膜抗原的分离的哺乳动物核酸分子。 本发明还提供能够与编码哺乳动物前列腺特异性膜抗原的核酸分子的序列特异性杂交的至少15个核苷酸的前列腺特异性膜核酸。 本发明进一步提供前列腺特异性膜抗原的载体和载体宿主表达系统。 本发明还提供了鉴定与前列腺特异性膜抗原结合的配体的生成抗体以产生针对完整的前列腺特异性膜抗原或部分抗原的抗体的方法。 本发明还提供了纯化的前列腺特异性膜抗原。 本发明提供一种治疗剂,其包含针对前列腺特异性膜抗原的抗体和与其缀合的细胞毒性剂。 本发明还提供了一种成像前列腺癌的方法和用于测量生物学简单的前列腺特异性膜抗原的量的免疫测定法。 本发明还提供了转基因非人哺乳动物,其包含编码哺乳动物前列腺特异性膜抗原的分离的核酸分子。
    • 84. 发明申请
    • Pharmacological targeting of bacterial DNA ligase for treatment and prevention of bacterial infections
    • 细菌DNA连接酶的药理学靶向用于治疗和预防细菌感染
    • US20060134642A1
    • 2006-06-22
    • US10935291
    • 2004-09-07
    • Stewart ShumanVerl Sriskanda
    • Stewart ShumanVerl Sriskanda
    • C12Q1/68C07H21/04C12N9/06C12N15/74C12N1/21
    • C12N9/93
    • This invention provides methods for the discovery of molecules that target an essential step of bacterial DNA replication—the sealing of DNA strands by NAD+-dependent DNA ligase. Specific structural components of NAD+-dependent DNA ligase that are important for the reaction of DNA ligase with NAD+ and that comprise a putative binding site for the NMN component of NAD+ were identified. The invention also includes recombinant DNA ligase enzymes that are defective in their reaction with NAD+, but active in the ligation of pre-adenylated DNA nicks. An underlying principle of this invention is the use of NAD+-reactive and NAD+-defective ligases to identify molecules that specifically bind to the NAD+-binding site of DNA ligase and thereby interfere with the reaction of DNA ligase with NAD+.
    • 本发明提供了发现靶向细菌DNA复制的必需步骤的分子的方法 - 通过NAD +依赖性DNA连接酶密封DNA链。 对DNA连接酶与NAD +的反应重要的NAD + / - 依赖性DNA连接酶的特异性结构组分,其包含NMNA NMNA成分的推定结合位点, SUP> + 。 本发明还包括与NAD + +反应有缺陷的重组DNA连接酶,但在腺苷酸化DNA缺口连接中是有活性的。 本发明的基本原理是使用NAD +反应性和NAD + - 有效连接酶来鉴定特异性结合NAD + / SUP- DNA连接酶的结合位点,从而干扰DNA连接酶与NAD +的反应。