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. 1999 Jul 12;146(1):13–28. doi: 10.1083/jcb.146.1.13

Figure 1.

Figure 1

Specificity of affinity-purified anti-Drosophila Bub1 antibodies. Identical amounts of Drosophila third instar larval brain extracts, from either wild-type (Oregon R) or bub1 mutant homozygotes, were loaded onto the indicated lanes of a Western blot probed with affinity-purified anti-Drosophila Bub1 antibodies (see Materials and Methods). A doublet of ∼165 kD (the predicted size for Drosophila Bub1) is recognized in wild-type extracts. These two bands are almost completely absent in brain extracts made from bub1 mutant brains. The antibody also recognizes a band of ∼100 kD that is not Bub1-specific and that is also recognized by pre-immune IgY. This cross-reacting band serves as an internal loading control.