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    • 6. 发明授权
    • Toxin genes and methods for their use
    • 毒素基因及其使用方法
    • US09556255B2
    • 2017-01-31
    • US13893763
    • 2013-05-14
    • Athenix Corporation
    • Kimberly S. SampsonDaniel J. Tomso
    • C12N15/82C07K14/325C07K16/12
    • C07K14/325A01N37/18C07K16/1278C12N15/8286Y02A40/162
    • Compositions and methods for conferring pesticidal activity to bacteria, plants, plant cells, tissues and seeds are provided. Compositions comprising a coding sequence for a delta-endotoxin polypeptide are provided. The coding sequences can be used in DNA constructs or expression cassettes for transformation and expression in plants and bacteria. Compositions also comprise transformed bacteria, plants, plant cells, tissues, and seeds. In particular, isolated delta-endotoxin nucleic acid molecules are provided. Additionally, amino acid sequences corresponding to the polynucleotides are encompassed, and antibodies specifically binding to those amino acid sequences. In particular, the present invention provides for isolated nucleic acid molecules comprising nucleotide sequences encoding the amino acid sequence shown in SEQ ID NO:61-121 and 133-141, or the nucleotide sequence set forth in SEQ ID NO:1-60, 124-132, and 142-283, as well as variants and fragments thereof.
    • 提供了赋予细菌,植物,植物细胞,组织和种子的杀虫活性的组合物和方法。 提供了包含δ-内毒素多肽的编码序列的组合物。 编码序列可用于DNA构建体或表达盒中,用于在植物和细菌中转化和表达。 组合物还包括转化的细菌,植物,植物细胞,组织和种子。 特别地,提供了分离的δ-内毒素核酸分子。 另外,包括对应于多核苷酸的氨基酸序列,以及与这些氨基酸序列特异性结合的抗体。 特别地,本发明提供了分离的核酸分子,其包含编码SEQ ID NO:61-121和133-141所示的氨基酸序列的核苷酸序列或SEQ ID NO:1-60,124所示的核苷酸序列 -132和142-283,以及其变体和片段。
    • 8. 发明授权
    • Glycosylated protein expression in prokaryotes
    • 原核生物中糖基化蛋白的表达
    • US09512434B2
    • 2016-12-06
    • US14630308
    • 2015-02-24
    • Cornell Research Foundation, Inc.
    • Matthew DelisaCassandra GuarinoThomas MansellAdam Fisher
    • C12N15/70C12N9/10C12N9/14
    • C12N15/70C07K16/1278C07K2317/21C07K2317/41C12N9/1048C12N9/1051C12N9/14C12P21/005C12Y204/01132C12Y204/01142C12Y204/01255C12Y204/01257C12Y306/03001
    • The present invention relates to a prokaryotic host cell comprising eukaryotic glycosyltransferase activity, where the eukaryotic glycosyltransferase activity is eukaryotic dolichyl-linked UDP-GlcNAc transferase activity and eukaryotic mannosyltransferase activity. Also disclosed is a method of producing a glycosylated protein by providing a prokaryotic host cell comprising the eukaryotic glycosyltransferase activity and culturing the prokaryotic host cell under conditions effective to produce a glycosylated protein. Another aspect of the present invention pertains to a method for screening bacteria or bacteriophages by expressing one or more glycans on the surface of a bacteria, attaching a label on the one or more glycans on the surface of the bacteria or on the surface of a bacteriophage derived from the bacteria, and analyzing the label in a high-throughput format. A glycosylated antibody comprising an Fv portion which recognizes and binds to a native antigen and an Fc portion which is glycosylated at a conserved asparagine residue is also disclosed.
    • 本发明涉及包含真核糖基转移酶活性的原核宿主细胞,其中真核糖基转移酶活性是真核的二酰基连接的UDP-GlcNAc转移酶活性和真核的甘露糖基转移酶活性。 还公开了通过提供包含真核糖基转移酶活性的原核宿主细胞并在有效产生糖基化蛋白的条件下培养原核宿主细胞来生产糖基化蛋白的方法。 本发明的另一方面涉及通过在细菌表面上表达一种或多种聚糖以在细菌表面上或噬菌体的表面上附着一个或多个聚糖上的标记物来筛选细菌或噬菌体的方法 衍生自细菌,并以高通量格式分析标签。 还公开了包含识别和结合天然抗原的Fv部分的糖基化抗体和在保守的天冬酰胺残基处被糖基化的Fc部分。