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. 2000 Dec;122(3):429–436. doi: 10.1046/j.1365-2249.2000.01363.x

Fig. 2.

Fig. 2

Western blot identification of human (lane 1) and bovine (lane 2) MBP using 1H6.2 and 45.30 MoAbs. To compare the reactivity of 1H6.2 and 45.30, a commercially available anti-MBP MoAb was used (anti-MBP recognizing epitope 84-89; Serotec, Oxford, UK). The typical major 18·5-kD MBP band is recognized by both 1H6.2 and 45.30 MoAbs. MBP has a reduced electrophoretic mobility due to its positive charge and runs at approximately the 21 kD level under these experimental conditions [24,25].