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Protein Assays
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Protein Assays Frequently Asked Questions
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Protein Assays
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Click a question below to see the answer:
How is the protein concentration determined?
Can I prepare several chips in advance?
Does the chip come prefilled with gel?
Is there a sample preparation required?
What are the storage conditions of the kits?
What is the shelf life of the kits?
How to validate the qualitative and quantitative range?
Is there sample carryover from one well to the next?
Is the High Sensitivity Protein 250 labeling charge-matched?
Which factors influence High Sensitivity Protein 250 labeling efficiency?
Does pH effect the labeling of the High Sensitivity Protein 250 assay?
Is it possible to run a sample with 10 % DMSO?
Is it possible to use the Protein assays in a QC environment?
How many samples can I load on a chip?
How long does it take to run a chip?
Is it possible to run a partial chip?
Which dye is used for detection?
Is it possible to use a different dye?
Does the intercalating dye stain all proteins with the same efficiency?
What separation matrix is used for the protein separation?
Are assays available that separate proteins by pl?
Can you analyze peptides or protein below 5 kDa?
Can the protein assays replace classical 2D gel electrophoresis?
Is it possible to run protein samples under native conditions?
Is it possible to analyze changes in protein expression in a cell lysate?
