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  Indian J Med Microbiol
 

Figure 6: Enzyme-linked oligonucleotide assays (ELONA) for binding site confirmation. The polyA tail RNA aptamer (100 nM) was immobilized onto ELISA microplate. The competitive inhibition of aptamer binding was measured by quantifying the absorbance of bound rhCD36 in the presence of mAb FA6-152. The data obtained were compared with control (in the absence of mAb FA6-152). Data analysis was done using Two-way ANOVA (Multiple comparisons test) where *P < 0.05 and **P < 0.01. Error bar indicates ±SD of the triplicate experiment.

Figure 6: Enzyme-linked oligonucleotide assays (ELONA) for binding site confirmation. The polyA tail RNA aptamer (100 nM) was immobilized onto ELISA microplate. The competitive inhibition of aptamer binding was measured by quantifying the absorbance of bound rhCD36 in the presence of mAb FA6-152. The data obtained were compared with control (in the absence of mAb FA6-152). Data analysis was done using Two-way ANOVA (Multiple comparisons test) where *<i>P</i> < 0.05 and **<i>P</i> < 0.01. Error bar indicates ±SD of the triplicate experiment.