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We mapped several resistance QTLs to bacterial blight in rice using a reference recombinant inbred lines derived from the cross between Azucena and IR64 rice varieties.
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GLA is produced using a recombinant DNA technology.
Protein levels were determined using a recombinant TK1 standard curve.
Filgrastim was expressed using a recombinant Escherichia coli strain.
From our previous quantitative trait locus (QTL) analysis, we had success in using a relatively small reference population of recombinant inbred strains of mice (AXBXA) to identify a genetic region that is significantly correlated with NPC proliferation in the RMS.
Mean intensities in the nucleus and the whole cell were converted to GFP concentrations by using a dilution series of recombinant SBP-GFP in PBS and embedded in 15% polyacrylamide gel as reference.
The bead-based assay used a recombinant protein heterotrimer that was heavily skewed toward A2B BLyS/APRIL trimers as a reference standard, but nevertheless, was also able to detect AB2 trimers.
To confirm the direct interaction, we used a recombinant protein.
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