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With further increase in pH, no significant change in dye binding capacity was observed.
From the results it was concluded that greater binding capacity was observed in polymer prepared in 10 mL of chloroform (Fig. 5).
Interestingly, a higher CXCL12 binding capacity was observed ex vivo in all lines of synovial origin (either OA or RA) compared with non-synovial ECs (HUVECs), and this may relate to features specific to either the tissue or vessel type.
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No significant differences in dynamic binding capacity were observed among human antibodies on MabSelect SuRe (∼20 40 mg/mL resin) and IgSelect (∼10 30 mg/mL resin).
However, as the pH of the dye solution increases, a considerable increase in dye binding capacity is observed due to strong electrostatic attraction between negatively charged sites on the biosorbent and the dye cations.
When between trial variations in HSP72 binding capacity were observed, relative differences in HSP72 binding affinity for the various peptides were maintained.
Degradation was negligible and a good swelling capacity was observed.
No specific neutralising capacity was observed for any prebleed serum.
The binding capacity was measured to be up to 44.45 mg (fluoride)/g (NPs) (10 times higher than 4 7 mg/g observed for hydroxyapatite [16,25]).
The dynamic binding capacity was determined.
The binding capacity was evaluated by frontal analysis.
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