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Fusion proteins bound to sepharose beads were quantitated by Commassie blue staining on SDS-polyacrylamide gels.
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Individual protein bands were quantitated by densitometry.
The ePCR was carried out on a SOLID EZ Bead amplifier and the enriched beads were quantitated using a NanoDrop 2000 spectrophotometer.
Scanned images were quantitated by Illumina Beadscan, v3.
Reads were quantitated by counting the number of reads across exons.
Infected cells were quantitated by fluorescence microscopy and automated image analysis.
Culture results were quantitated by organism.
Cytokine levels in synovial fluid were quantitated by Multiplex ELISA.
Cytokine levels in synovial fluid before ACL reconstruction surgery were quantitated by Multiplex ELISA.
Cleavage fractions were quantitated by phosphorimaging.
ChIP samples were quantitated by real-time PCR.
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