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    • 51. 发明公开
    • 단백질 나노입자를 이용한 3차원 나노구조체
    • 蛋白纳米颗粒的三维纳米结构域
    • KR1020120101961A
    • 2012-09-17
    • KR1020110020130
    • 2011-03-07
    • 고려대학교 산학협력단
    • 이지원서혁성
    • G01N33/68C12Q1/68G01N33/574B82Y15/00
    • G01N33/68B82Y15/00C12Q1/68G01N33/683
    • PURPOSE: A three dimensional nanostructure using protein nanoparticles is provided to detect a target material. CONSTITUTION: A method for preparing a protein-DNA multilayer nanostructure comprises: a step of fixing a control protein of which net charge changes at a substrate according to pH concentration except for a metal nano dot; a step of changing pH concentration to adjust the net charge of the control protein; and a step of laminating a DNA layer and a protein layer on the metal nano dot. The protein layer contains allogenic or xenogenic protein particles. The substrate is formed of metal, nickel. [Reference numerals] (AA) Gold; (BB) Nickel layer; (CC) Si wafer; (DD) Adding (his)6-tagged proteasome alpha particles(pH 7.4, 8); (EE) Adding ssDNA(polyA, 20bp), conversion to pH 5; (FF) Adding DPS particles[first layer formation], conversion to pH 8; (GG) Adding dsDNA(519bp), conversion to pH 5; (HH) Adding DPS particles[second layer formation], moving to pH 8; (II) Adding dsDNA(519bp), conversion into pH 5; (JJ) Adding DPS particles[third layer formation], conversion to pH 8; (KK) Type 1 DPS particle layers; (LL) Type 2 DPS particle layers; (MM) N layer formation on fourth layer; (NN) Type 1 DPS particles for capturing antibody marker 1; (OO) Antigen peptide fixed on the surface, which specifically binds to antibody marker 1; (PP) Type 2 DPS particles for capturing antibody marker 2; (QQ) Antigen peptide fixed on the surface, which specifically binds to antibody marker 2; (RR) Simultaneous detection and diagnosis system(example)
    • 目的:提供使用蛋白质纳米颗粒的三维纳米结构以检测靶材料。 构成:制备蛋白质-DNA多层纳米结构体的方法包括:除了金属纳米点之外,根据pH浓度固定基底上的净电荷变化的对照蛋白质的步骤; 改变pH浓度以调整对照蛋白的净电荷的步骤; 以及在金属纳米点上层叠DNA层和蛋白质层的步骤。 蛋白质层含有异源或异种蛋白质颗粒。 基板由金属,镍形成。 (附图标记)(AA)金; (BB)镍层; (CC)Si晶片; (DD)添加(他的)6标记的蛋白酶体α粒子(pH 7.4,8); (EE)加入ssDNA(polyA,20bp),转化为pH 5; (FF)添加DPS颗粒[第一层形成],转化为pH8; (GG)加入dsDNA(519bp),转化为pH 5; (HH)添加DPS颗粒[第二层形成],移至pH8; (II)加入dsDNA(519bp),转化为pH5; (JJ)添加DPS颗粒[第三层形成],转化为pH8; (KK)1型DPS颗粒层; (LL)2型DPS颗粒层; (MM)N层形成在第四层上; (NN)用于捕获抗体标记物1的1型DPS颗粒; (OO)固定在表面上的抗原肽,其特异性结合抗体标记物1; (PP)用于捕获抗体标记物2的2型DPS颗粒; (QQ)固定在表面上的抗原肽,其特异性结合抗体标记物2; (RR)同步检测和诊断系统(示例)
    • 58. 发明申请
    • Test for the rapid evaluation of ischemic states and kits
    • 测试缺血状态和试剂盒的快速评估
    • US20050142613A1
    • 2005-06-30
    • US11033766
    • 2005-01-12
    • David Bar-OrEdward LauJames WinklerGary FaganHollie Wayment
    • David Bar-OrEdward LauJames WinklerGary FaganHollie Wayment
    • G01N33/68G01N33/53C07K14/765
    • G01N33/6842G01N33/683
    • The present invention relates to rapid methods for the detection of ischemic states and to kits for use in such methods. Provided for is a rapid method of testing for and quantifying ischemia based upon methods of detecting and quantifying the existence of an alteration of the serum protein albumin which occurs following an ischemic event; methods for detecting and quantifying this alteration include evaluating and quantifying the cobalt binding capacity of circulating albumin, analysis and measurement of the ability of serum albumin to bind exogenous cobalt, detection and measurement of the presence of endogenous copper in a purified albumin sample and use of an immunological assay specific to the altered form of serum albumin which occurs following an ischemic event. Also taught by the present invention is the detection and measurement of an ischemic event by measuring albumin N-terminal derivatives that arise following an ischemic event, including truncated albumin species lacking one to four N-terminal amino acids or albumin with an acetylated N-terminal Asp residue.
    • 本发明涉及用于检测缺血状态的快速方法和用于这些方法的试剂盒。 基于检测和定量缺血事件发生的血清蛋白白蛋白变化的存在的方法,提供了一种快速测试和定量缺血的方法; 用于检测和定量这种改变的方法包括评估和定量循环白蛋白的钴结合能力,分析和测量血清白蛋白结合外源钴的能力,检测和测量纯化白蛋白样品中内源性铜的存在,以及使用 在缺血事件之后发生的血清白蛋白改变形式的特异性免疫测定。 本发明还教导了通过测量缺血事件后出现的白蛋白N末端衍生物检测和测量缺血事件,包括缺乏一至四个N-末端氨基酸的截短的白蛋白物质或具有乙酰化N-末端的白蛋白 Asp残基。