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    • 1. 发明授权
    • Fourier transform surface plasmon resonance adsorption sensor instrument
    • 傅里叶变换表面等离子共振吸收传感器仪器
    • US06330062B1
    • 2001-12-11
    • US09303260
    • 1999-04-30
    • Robert M. CornMichael J. GreenStephen C. WeibelTony G. Frutos
    • Robert M. CornMichael J. GreenStephen C. WeibelTony G. Frutos
    • G01N2155
    • G01N21/35G01N21/359G01N21/553
    • Adsorption of molecules onto a thin metallic surface such as of gold, silver or copper is measured by surface plasmon resonance (SPR) using Fourier Transform (FT) spectroscopy. Reflectance spectra from a prism/metallic film sample surface at a fixed angle of incidence is measured with FT spectroscopy. The reflectance spectrum exhibits a pronounced minimum due to the SPR effect, which can be shifted by changing the angle of incidence or metallic film thickness. The position of the reflectance minimum shifts in wavelength with the adsorption of molecules onto the gold surface due to a change in the index of refraction at the interface. The FT-SPR sensor instrument provides wavelength stability and reproducibility of the resonance wavelength to permit detection of small wavelength shifts, and also substantially increases the spectral range over which the SPR measurements can be made. A beam of broadband radiation from a Michelson interferometer is directed through an SPR sample cell and onto a detector where the output signal is processed using standard FT techniques.
    • 使用傅立叶变换(FT)光谱法,通过表面等离子体共振(SPR)测量分子到金,银或铜等金属表面上的吸附。 用FT光谱法测量来自固定入射角的棱镜/金属膜样品表面的反射光谱。 由于SPR效应,反射光谱显示出明显的最小值,可通过改变入射角或金属膜厚度来移动反射光谱。 由于界面处的折射率的变化,反射率最小值的位置随着分子吸附在金表面上而波长的偏移。 FT-SPR传感器仪器提供了波长稳定性和谐振波长的再现性,以允许检测小的波长位移,并且还大大提高可以进行SPR测量的光谱范围。 来自迈克尔逊干涉仪的宽带辐射波束通过SPR采样单元引导到检测器上,其中使用标准FT技术处理输出信号。
    • 8. 发明授权
    • Process to create biomolecule and/or cellular arrays on metal surfaces
and product produced thereby
    • 在金属表面上产生生物分子和/或细胞阵列的方法和由此产生的产物
    • US6127129A
    • 2000-10-03
    • US368991
    • 1999-08-05
    • Robert M. CornAnthony G. FrutosJennifer M. Brockman
    • Robert M. CornAnthony G. FrutosJennifer M. Brockman
    • G01N33/566B01J19/00C12M1/00C12N15/09C12Q1/68G01N33/53G01N33/543G01N33/553G01N37/00G03F9/00
    • B82Y30/00
    • Disclosed is a process to construct multi-component biomolecule or cellular arrays suitable for use in SPR imaging studies of large molecule, cellular/molecular, and cell/cell interactions. The success of the procedure hinges on the use of a reversible protecting group to modify reversibly .omega.-functionalized alkanethiols self-assembled on metal substrates.
    • 本发明提供编码哺乳动物甘氨酸转运蛋白的分离的核酸分子,编码人甘氨酸转运蛋白的分离的核酸分子,作为哺乳动物甘氨酸转运蛋白的分离的蛋白质,作为人甘氨酸转运蛋白的分离的蛋白质,包含编码哺乳动物的分离的核酸分子的载体 或人甘氨酸转运蛋白,包含此类载体的哺乳动物细胞,针对哺乳动物甘氨酸转运蛋白的抗体,针对人甘氨酸转运蛋白的抗体,用于检测编码哺乳动物甘氨酸转运蛋白的核酸的核酸探针,用于检测核酸编码的核酸探针 人甘氨酸转运蛋白,与编码哺乳动物甘氨酸转运蛋白的核酸分子的任何序列互补的反义寡核苷酸,与编码人甘氨酸转运蛋白的核酸所述分子的任何序列互补的反义寡核苷酸,ph 与哺乳动物甘氨酸转运蛋白和非人转运蛋白相关的药物化合物,与人甘氨酸转运蛋白相关的药物化合物和非人类转基因动物,其表达编码正常或突变型哺乳动物或人甘氨酸转运蛋白的DNA。 本发明还提供了用于确定配体结合,检测表达,药物筛选和用于减轻与哺乳动物甘氨酸转运蛋白相关的异常的治疗的方法。 本发明还提供了用于确定配体结合,检测表达,药物筛选和用于减轻与人甘氨酸转运蛋白相关的异常的治疗的方法。