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DynaPro NanoStar manual - Department of Physiology and Biophysics

DynaPro NanoStar manual - Department of Physiology and Biophysics

DynaPro NanoStar manual - Department of Physiology and Biophysics

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Correlation FunctionSample vs. SolventNot all samples can be measured, nor are all samples properly suited formeasurement by <strong>DynaPro</strong> instruments, <strong>and</strong> therefore not all samplesproduce valid correlation functions. Without a valid correlation function, itis not possible to determine a valid size distribution.A valid correlation function is generally smooth <strong>and</strong> continuous, exponentiallydecaying from a maximum value <strong>of</strong> 2 to a value <strong>of</strong> 1.The following figure shows a valid correlation function. Visually, weobserve one decay in the function.The function contains r<strong>and</strong>om values centered around 1, asymptoticallyreaching 1. R<strong>and</strong>omness represents the result from measuring puresolvent: solution containing zero analyte or analyte below the limits <strong>of</strong>detection. The size distribution analysis attempts to find a result for thesefunctions. These must be marked <strong>and</strong> removed from the analysis. It is generallya good idea to measure the solvent to confirm its purity. If youunexpectedly see a function characteristic <strong>of</strong> a solvent, increase the laserpower, measure the sample unfiltered (to avoid potential binding to themembrane) or uncentrifuged, <strong>and</strong>/or increase the concentration <strong>of</strong> theanalyte.DYNAMICS User’s Guide (M1400 Rev. K) 8-13

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