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SPRpages homeSite about Surface Plasmon Resonance and Biomolecular Interaction Analysis.
http://www.sprpages.nl/
Site about Surface Plasmon Resonance and Biomolecular Interaction Analysis.
http://www.sprpages.nl/
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SPRpages home | sprpages.nl Reviews
https://sprpages.nl
Site about Surface Plasmon Resonance and Biomolecular Interaction Analysis.
sprpages.nl
Dissociation
http://www.sprpages.nl/kinetics/dissociation
When the analyte in the flow over the surface of the chip is replaced by the flow buffer, the free concentration of the analyte suddenly drops to zero and the complex will start to dissociate. If rebinding of released analyte can be ignored, dissociation can be described by the rate equation (1). Or the linearized form. In theory, the dissociation rate constant (. Like the association it is better / easier to fit the integrated rate equation to the experimental data:. Or rebinding of analyte (6). Then di...
Forum :: Category index
http://www.sprpages.nl/kunena/index.html
Forum : Category index. The SPRpages invites you to post your questions and comments on Surface Plasmon Resonace and Biomolecular Interaction Analysis . This is the general discussion forum of the SPR-pages. Last Post: New LinkedIn Group- . 26 Aug 2016 16:03. These are the posts of the old forum. 22 Dec 2013 19:44.
SPR History
http://www.sprpages.nl/spr-overview/spr-history
Between 1902 and 1912 R.M. Wood (1868-1955) at Johns Hopkins University (Baltimore, USA) noticed that when he shone polarized light onto a metal-backed diffraction grating, a pattern of unusual dark and light bands appeared in the reflected light (1). Although he speculated about how the light, gratings and metal interacted, a clear answer to the pheno menon was not provided. The first theoretical treatment of these anomalies was by Lord Rayleigh in 1907 (3). Wood's later papers, (5). There have been two...
Experiments
http://www.sprpages.nl/experiments.html
The design of your experiment is very important for the end-result. Carefully planned experiments with the proper controls will give to the best results with a minimum in experimental time. This part wil help you to make the right decisions for your situation. Take some time to plan your experiment and you will gain a lot of time when you analyse the results. Please read the Best results. Part about preparing your instrument for the best measurements. In addition, read the Sensor chips. PO4, 1.8 mM KH.
Artefacts
http://www.sprpages.nl/best-results/artifacts
Instead of applying different models in search of the best fit through the data, first, try to optimize the experimental conditions. There are three main groups of experimental artefacts to consider:. Including the instrument, the measuring cell, the matrix on which the ligand is bound, and the buffers. Is it pure and homogeneous? Does the immobilization destroy epitopes? How does it perform after regeneration? Is it reacting only with the ligand? Is it a monomer? Injecting a volume of flow buffer over a...
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References | Affinite Instruments
http://affiniteinstruments.com/references
One Chip = Triplicate Reference. News & References. One Chip = Triplicate Reference. News & References. 1 Zhao SS., et al., Miniature multi-channel SPR instrument for methotrexate monitoring in clinical samples. Biosensors and Bioelectronics, 2015, 64. 2 Yockell-Lelièvre H., et al. Plasmonic sensors for the competitive detection of testosterone. The Analyst, 2015, 140. 3 Homola J. et al., Surface plasmon resonance sensors for detection of chemical and biological species. Chemical Reviews, 2008, 108.
Resources and Links › NMR Structural Biology Facility & Biophysical Core Facility › UConn Health
http://structbio.uchc.edu//resources
The Gregory P. Mullen. NMR Structural Biology Facility and Biophysical Core Facility. Instruments and Protein Expression Services. Circular Dichroism (CD) Instrumentation. Surface Plasmon Resonance (SPR) Instrumentation. Isothermal Titration Calorimetry (ITC) Instrumentation. Installation of 800 Instrument. Biological Magnetic Resonance Data Bank (BMRB). A repository for data from NMR spectroscopy on proteins, peptides, nucleic acids, and other biomolecules. Protein NMR: A practical guide.
Resources and Links › NMR Structural Biology Facility & Biophysical Core Facility › UConn Health
http://structuralbiology.uchc.edu//resources
The Gregory P. Mullen. NMR Structural Biology Facility and Biophysical Core Facility. Instruments and Protein Expression Services. Circular Dichroism (CD) Instrumentation. Surface Plasmon Resonance (SPR) Instrumentation. Isothermal Titration Calorimetry (ITC) Instrumentation. Installation of 800 Instrument. Biological Magnetic Resonance Data Bank (BMRB). A repository for data from NMR spectroscopy on proteins, peptides, nucleic acids, and other biomolecules. Protein NMR: A practical guide.
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How low can you go? In SPR experiments, low responses are preferred over high responses. This is because high responses in general are affected by mass transport and non 1:1 interactions. But how low can you go? This depends in the first place on the instrument you have chosen. The signal should be above the noise level of the baseline. The curves should be easily recognisable and replicates should overlay. Read more on low responses. 25 years of SPR. Read more on 25 years of development. And learn all t...
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