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ProteOn XPR36 System | C Surface Plasmon Resonance
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Regeneration Step
If an immobilized ligand surface is going to be used in another set of
experiments, any remaining bound analyte must be removed first. In some
cases, particularly with small-molecule interactions, this can be accomplished
after the dissociation phase, simply by flowing buffer long enough for
complete dissociation to occur. If this is insufficient, or removal takes too long
to be practical, the remaining analyte is removed using a regeneration step in
which acidic, basic, ionic, or detergent-containing buffer is passed over the
sensor chip surface.
For effective regeneration, the buffer must be able to strip off the bound
analyte, but maintain the activity of the immobilized ligand. Use high flow
rates and minimal volumes (100 μl/min and 30 μl, for example) to minimize
damage to the ligand. The ProteOn Regeneration Buffer Kit contains nine of
the most commonly used regeneration solutions.
Summary of Contents for XPR36
Page 1: ...ProteOn XPR36 Protein Interaction Array System Protein Interaction Analysis User Manual...
Page 2: ......
Page 3: ...ProteOn XPR36 Protein Interaction Array System Version 3 1 User Manual...
Page 4: ......
Page 10: ...ProteOn XPR36 System viii...
Page 166: ...ProteOn XPR36 System Analysis 148...
Page 188: ...ProteOn XPR36 Maintenance 170...
Page 194: ...ProteOn XPR36 System ProteOn System Troubleshooting 176...
Page 226: ...ProteOn XPR36 System A ProteOn XPR36 Instrument and Peripherals 208...
Page 250: ...ProteOn XPR36 System E Ordering Information 232...
Page 264: ...ProteOn XPR36 System F Security Edition Configuration Guide 246...
Page 276: ...ProteOn XPR36 System Glossary 258...
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