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    • 4. 发明申请
    • STANDARD
    • 标准
    • WO2005003773A1
    • 2005-01-13
    • PCT/IB2004/002682
    • 2004-07-08
    • DAKOCYTOMATION DENMARK A/SWINTHER, LarsPII, Kurt
    • WINTHER, LarsPII, Kurt
    • G01N33/543
    • G01N33/5005C12Q1/6841G01N1/36G01N33/54346G01N33/54353G01N33/54386G01N33/96G01N2001/2893G01N2496/00C12Q2545/113
    • We disclose a reference standard for a detectable entity, the reference standard comprising a support medium, preferably an embedding medium, a compact particle having a compact shape with a quantity of detectable entity coupled thereto and supported by the medium, in which the compact particle is a biological, preferably cellular compact particle, preferably a cellular compact particle. We also disclose a reference standard for a detectable entity, the reference standard comprising a support medium, preferably an embedding medium, a compact particle having a compact shape with a quantity of detectable entity coupled thereto and supported by the medium, in which the compact particle is a non-biological compact particle, preferably a non-cellular compact particle having cell-like dimensions, preferably less than 1.5 mm.
    • 我们公开了可检测实体的参考标准,参考标准包括支持介质,优选包埋介质,具有紧凑形状的致密颗粒,其具有耦合到其上并由介质支持的可检测实体的量,其中紧密颗粒是 生物的,优选细胞致密的颗粒,优选细胞致密颗粒。 我们还公开了可检测实体的参考标准,参考标准包括支持介质,优选包埋介质,具有紧凑形状的致密颗粒,其具有与其连接并由介质支持的可检测实体的量,其中致密颗粒 是非生物致密颗粒,优选具有细胞样尺寸,优选小于1.5mm的非细胞致密颗粒。
    • 7. 发明申请
    • STANDARD FOR IMMUNOHISTOCHEMISTRY, IMMUNOCYTOCHEMISTRY AND MOLECULAR CYTOGENETICS
    • 免疫组织化学,免疫组织化学和分子细胞化学标准
    • WO2004077057A1
    • 2004-09-10
    • PCT/IB2004/001173
    • 2004-02-27
    • DAKOCYTOMATION DENMARK A/SWINTHER, Lars
    • WINTHER, Lars
    • G01N33/53
    • G01N15/1468C12Q1/6841G01N1/06G01N1/36G01N2001/2893G01N2015/1472
    • We describe a method comprising: (a) providing a reference standard or a planar section thereof, the reference standard comprising (i) a support medium; and (ii) a quantity of a detectable entity supported by the support medium; in which the detectable entity has an elongate path; in which a predetermined amount of the detectable entity is present in a defined region in a cross section of the reference standard; (b) obtaining a first reference signal indicative of the presence or quantity of detectable entity in the reference standard, planar section thereof, or the defined region; (c) providing a biological sample and obtaining a second signal indicative of the presence or quantity of detectable entity in the biological sample, or a component thereof; and (d) comparing the reference signal obtained in (b) against the second signal obtained in (c). Preferably, the method is used to indicate the presence, quantity or concentration of a detectable entity in a biological sample.
    • 我们描述了一种方法,包括:(a)提供参考标准或其平面部分,所述参考标准包括(i)支撑介质; 和(ii)由支持媒介支持的可检测实体的数量; 其中可检测实体具有细长路径; 其中预定量的可检测实体存在于参考标准的横截面中的限定区域中; (b)获得指示参考标准,其平面部分或限定区域中可检测实体的存在或数量的第一参考信号; (c)提供生物样品并获得指示生物样品或其组分中可检测实体的存在或数量的第二信号; 和(d)将(b)中获得的参考信号与(c)中获得的第二信号进行比较。 优选地,该方法用于指示生物样品中可检测实体的存在,数量或浓度。
    • 9. 发明申请
    • PROCESS AND APPARATUS FOR PREPARING AND PRESENTING A TISSUE SAMPLE FOR HISTOLOGICAL STUDY
    • 制备和提供组织学研究的组织样品的方法和装置
    • WO2003016872A1
    • 2003-02-27
    • PCT/DK2002/000532
    • 2002-08-12
    • DAKOCYTOMATION DENMARK A/SHUANG, Dennis, ShihchangWINTHER, Lars
    • HUANG, Dennis, ShihchangWINTHER, Lars
    • G01N1/36
    • G01N1/36G01N1/06G01N1/30Y10T436/2525
    • An apparatus and method for preserving cytological specimens for histological or histopathological use. A cytological sample from a biological tissue such as a tumor or a tumor cell line is dehydrated, disbursed and evenly distributed throughout a volume of molten material. The molten material is then drawn into a tubular member such as a pipette and allowed to solidify. Upon solidification, the cylindrical specimen is partially or completely extrudedfrom the tube for further processing, including fixation, dehydration and molten paraffin infiltration and embedding as required for presentation to a sectioning device such as a microtome. Thin circular slices of the cylindrical specimen are removed from the cylindrical specimen and transferred to a slide, fixed and stained as desired. The device and method enable the production of a slide bearing a spatially homogeneous distribution of cytological material for microscopic examination.
    • 一种用于保留细胞学标本用于组织学或组织病理学用途的装置和方法。 来自生物组织如肿瘤细胞系的细胞学样品被脱水,分散并均匀分布在一定体积的熔融材料中。 然后将熔融的材料拉入诸如移液管的管状构件中并使其固化。 固化后,将圆筒形样品从管中部分或完全挤出,用于进一步加工,包括固定,脱水和熔融石蜡渗透,并根据需要将其包埋到切片装置如切片机上。 将圆柱形试样的圆形圆形切片从圆柱形样品中取出并转移到载玻片上,固定并根据需要进行染色。 该装置和方法使得能够生产具有用于显微镜检查的细胞学材料的空间均匀分布的载玻片。
    • 10. 发明申请
    • METHOD FOR PURIFICATION OF TARGET POLYPEPTIDES
    • 目标多肽的纯化方法
    • WO2010128033A2
    • 2010-11-11
    • PCT/EP2010/056010
    • 2010-05-04
    • NOVOZYMES A/SKYHSE-ANDERSEN, JanWINTHER, Lars
    • KYHSE-ANDERSEN, JanWINTHER, Lars
    • C07K14/435C07K1/22
    • C07K1/22C07K1/32C07K1/36
    • The present invention relates to a process for purification of a target molecule, comprising the steps: (a) contacting a target molecule, and a population of target binding polypeptides (TBP), in solution for a sufficient time to allow complex formation; and (b) isolating the target from the complex from (a) by subsequent purification steps, wherein (i) the target binding polypeptides have at least two binding functionalities; a first binding functionality towards the target and a second binding functionality towards a catching ligand comprised in a solid support; and (ii) the first binding functionality comprises at least two binding sites for the target, and the target com¬ prises at least two binding sites for the TBP.
    • 本发明涉及一种纯化靶分子的方法,包括以下步骤:(a)在溶液中使目标分子和靶结合多肽(TBP)群体接触足够的时间以允许复合物形成; 和(b)通过随后的纯化步骤从(a)分离所述复合物中的靶,其中(i)靶结合多肽具有至少两个结合官能团; 针对靶的第一结合功能和朝向包含在固体支持物中的捕获性配体的第二结合功能; 和(ii)第一结合功能包含靶的至少两个结合位点,并且靶标包含TBP的至少两个结合位点。