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    • 21. 发明授权
    • Sheet-guiding device with a cooled sheet-guiding plate
    • 具有冷却片导板的片导向装置
    • US5992845A
    • 1999-11-30
    • US789487
    • 1997-01-27
    • Wolfram FendlerMatthias SchusterBurkhard MackBernhard Waltenberger
    • Wolfram FendlerMatthias SchusterBurkhard MackBernhard Waltenberger
    • B41F21/00B41F23/04B65H5/00B65H29/52B65H29/24
    • B41F23/04B65H29/52B65H2406/00
    • A sheet-guiding device with a cooled sheet-guiding plate formed with air outlet openings, the sheet-guiding plate having a sheet-guiding surface on one side thereof and being connected, at the other side thereof opposite to the one side, to coolant ducts permitting the air outlet openings to remain freely open, and a cooling-duct plate having deformations forming the coolant ducts, the cooling-duct plate being connected by welding to the sheet-guiding plate and being sealed with respect thereto, includes a sealing element disposed between the other side of the sheet-guiding plate and the cooling-duct plate, the sealing element being in a groove-shaped indentation formed in the cooling-duct plate and surrounding a respective air outlet opening, and welding zones located in the vicinity of the sealing element for forming a connection between the sheet-guiding plate and the cooling-duct plate by weldments.
    • 一种片材引导装置,其具有形成有排气口的冷却片材引导板,片材引导板在其一侧具有片材引导表面,并且在与其一侧相对的另一侧连接到冷却剂 允许空气出口开口保持自由打开的管道和具有形成冷却剂管道的变形的冷却管道板,冷却管道板通过焊接连接到片材引导板并相对于其密封,包括密封元件 所述密封元件设置在所述导板的另一侧与所述冷却管板之间,所述密封元件位于形成在所述冷却管道板中的槽形凹部中,并且包围相应的出气口,并且位于所述附近的焊接区域 用于通过焊件形成片材引导板和冷却管板之间的连接的密封元件。
    • 26. 发明申请
    • Method for Quantifying Methylated Dna
    • 甲基化Dna的定量方法
    • US20090004646A1
    • 2009-01-01
    • US11629743
    • 2005-06-15
    • Matthias SchusterPhilipp Schatz
    • Matthias SchusterPhilipp Schatz
    • C12Q1/68
    • C12Q1/6827C12Q2537/164C12Q2521/331
    • The inventive method makes it possible to quantify methylated DNA by combining the restricted digestion and real-time PCR. For this purpose, the inventive method consists in isolating the examined DNA from a biological sample, in reacting the isolated AND with a methylation specific restriction enzyme, in amplifying by means of a real-time PCR, wherein the amplified products are formed only when the DNA is precut-off and, afterwards, in calculated the methylated and unmethylated DNA proportion in the initial sample with the aid of a reference measurement. Said method is particularly suitable for diagnosis and prognosis cancer and other diseases associated with a methylation state modification and for predicting the drug effects.
    • 本发明的方法使得可以通过组合限制性消化和实时PCR来定量甲基化DNA。 为此目的,本发明的方法在于通过实时PCR扩增从分离出的生物样品中的DNA,使分离的AND与甲基化特异性限制酶反应,其中扩增产物仅在 DNA被去除,然后借助于参考测量计算初始样品中的甲基化和非甲基化DNA比例。 所述方法特别适用于与甲基化状态修饰相关的癌症和其他疾病的诊断和预后,并用于预测药物作用。
    • 30. 发明授权
    • Process for solid phase glycopeptide synthesis
    • 固相糖肽合成方法
    • US5369017A
    • 1994-11-29
    • US191777
    • 1994-02-04
    • Chi-Huey WongMatthias Schuster
    • Chi-Huey WongMatthias Schuster
    • C07K1/04C12P21/00
    • C07K1/042
    • A process for the synthesis of a glycopeptide using a solid phase matrix is disclosed. The matrix is compatible with aqueous and organic solvents and is comprised of a silica-based solid support to which is linked a two-part spacer group having a chain length of about 12 to about 40 methylene groups. The first part of the spacer is covalently bonded to the silica-based support and has a length of about 3 to about 10 methylene groups. The second spacer part is covalently bonded to the first part of the spacer and comprises the distal end of the two part spacer. The second part is soluble as a free molecule in each of water, dimethylformamide and dichloromethane and has a terminal amine or hydroxyl group to which the C-terminal residue of the peptide portion of the glycopeptide chain is bonded. The chain of atoms connecting the desired glycopeptide to the solid phase matrix also includes a moiety having a selectively severable bond which on cleavage of that bond separates the matrix from whatever else is bonded to that moiety.
    • 公开了使用固相基质合成糖肽的方法。 该基质与水性和有机溶剂相容,并且由二氧化硅基固体载体组成,其连接有链长约12至约40个亚甲基的两部分间隔基团。 间隔基的第一部分共价结合到二氧化硅基载体上,其长度为约3至约10个亚甲基。 第二间隔部分共价结合到间隔物的第一部分并且包括两部分间隔物的远端。 第二部分作为水,二甲基甲酰胺和二氯甲烷中的每一个中的游离分子是可溶的,并且具有结合糖肽链的肽部分的C末端残基的末端胺或羟基。 将所需糖肽连接到固相基质上的原子链还包括具有选择性可分离键的部分,其在该键的切割时将基质与与该部分键合的任何其它基团分开。