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. 2016 Jun 17;6(2):89–97. doi: 10.4314/ovj.v6i2.4

Fig. 1.

Fig. 1

RT-PCR amplification of the Newcastle disease virus fusion protein gene using F1 (forward) and R (reverse) primer combination, which gave a product size of 1412 bp. The amplicons were electrophoresed in 2% agarose gel. Lanes: M, molecular size marker; Lanes 1-7 are NDV strains I2, TY-1/90, C30, Dik-90, GD.S.1, Lasota and Dongola, respectively; Lane 8, –ve control (H2O).