Figure 1.
Figure 1. Validation of quantitative RT-PCR for FcγRII isoforms on the LightCycler. The products obtained in PCR were separated on 1% agarose gel. GUS, FcγRIIb2, and then FcγRIIa were loaded. The first 3 slots are the serial dilutions of the standard curve, followed by the nontemplate control, followed by duplicates of 2 samples.

Validation of quantitative RT-PCR for FcγRII isoforms on the LightCycler. The products obtained in PCR were separated on 1% agarose gel. GUS, FcγRIIb2, and then FcγRIIa were loaded. The first 3 slots are the serial dilutions of the standard curve, followed by the nontemplate control, followed by duplicates of 2 samples.

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