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. 2011 Apr 7;6(4):e18593. doi: 10.1371/journal.pone.0018593

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Banerjee et al.

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.

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(A) Staining of the subproteome of R. solani using a Sypro ruby stain. (B) An approximately 37 kDa putative receptor was identified in a ligand blot assay of the membrane subproteome of R. solani with mASAL when probed with an anti-ASAL antibody. (C) Ligand blot analysis of the subproteome with mASAL pre-saturated with excess α- D mannose and probed with an anti-ASAL antibody showed an absence of signal (D) Glycospecific-staining of subproteome indicated the glycoprotein nature of the putative receptor (arrowhead denoting an approximately 37-kDa receptor) (E) Staining of deglycosidase-treated subproteome by Sypro ruby stain (F) Ligand blot analysis of de-glycosylated subproteome probed with an anti-ASAL antibody showed no signal (G) A ligand blot assay of a subproteome without mASAL as a negative control (M) represents a standard Protein molecular weight marker.