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Optimizing antibody microarrays for high resolution SPR microscopy

机译:优化高分辨率SPR显微镜的抗体微阵列

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A high resolution surface plasmon resonance (SPR) microscopy technique based on the combination of Lumera's polymer and proprietary optic technologies offers parallel high-throughput analysis of biomolecular binding kinetics on high-density antibody microarrays ( > 1,500 spots in 1.4 cm~2). The high resolution SPR microscopy also shows potential as a quantitative drug screening tool (Binding kinetics of a 1500 Dal. peptide has been experimentally demonstrated). However, the high resolution SPR microscopy requires optimal surface modification and dense sample addressing technology. Another constraint for the high density biomolecular microarray experiment is maintaining the activity of proteins during the microarray fabrication process. In this report, various spotting solutions combined with different surface modification chemistries are evaluated for the uniformity and integrity of protein spots in microarrays. The effects of various spotting solution compositions on the protein activity resulting from the microarray fabrication process are also investigated
机译:基于Lumera的聚合物和专有光学技术组合的高分辨率表面等离子体共振(SPR)显微镜技术提供了高密度抗体微阵列的生物分子结合动力学的平行高通量分析(> 1.4cm〜2中的1,500点)。高分辨率SPR显微镜也显示出作为定量药物筛选工具的潜力(1500 DAL的结合动力学。肽已被实验证明)。然而,高分辨率SPR显微镜需要最佳的表面改性和密集样品寻址技术。高密度生物分子微阵列实验的另一个约束是在微阵列制造过程中保持蛋白质的活性。在本报告中,对微阵列中蛋白质点的均匀性和完整性评估了各种斑点与不同表面改性化学的各种斑点解决方案。还研究了各种斑点溶液组合物对微阵列制造过程产生的蛋白质活性的影响

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