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. 2000 Mar 1;19(5):913–920. doi: 10.1093/emboj/19.5.913

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Fig. 1. Detection of TMV MP-interacting protein in cell wall fraction by immunorecognition of bound MP. (A) Renatured blot overlay assay. Lane 1, cell wall fraction blot incubated with MP; lane 2, cell wall fraction blot incubated with buffer alone; lane 3, empty membrane incubated with TMV MP; lane 4, soluble fraction blot incubated with TMV MP. (B) Protein content of the cell wall and soluble fractions of tobacco leaf tissue. Both lanes represent protein extract derived from 10 mg of fresh tobacco leaf tissue. Lane 1, silver-stained cell wall proteins; lane 2, Coomassie blue-stained soluble proteins. The positions of the 38 kDa TMV MP-interacting protein on the blot (open arrowhead) and on stained SDS–polyacrylamide gels (filled arrowhead) are indicated. The numbers between panels indicate molecular mass standards in kDa.