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The relative similarity of tables was visualized in two ways.
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The numbers of differentially expressed proteins listed in these tables are visualized in Fig. 3.
Immunolabeling with the primary antibody listed in Table 1 was visualized using the streptavidin-biotin-peroxydase method, as previously described [8].
Differential expression of the genes included in Table 2 was visualized by a heat map obtained by hierarchical clustering (HCL), which generates a tree (dendrogram) to group similar objects together.
Sections were labeled with a rabbit anti-RET monoclonal antibody (1 1000 dilution, clone EPR2871, Epitomics, Burlingame, CA, USA; see Additional file 1 for antibody specificity and immunohistochemistry validation; Additional file 1: Table S1) and RET expression was visualized with EnVision™ FLEX+ (Dako, #K8012).
In total, we detected 31 twins in the M. graminicola progenies, whose identity was visualized by graphical genotyping (Table S12).
EGFP was visualized directly.
EGFP fluorescence was visualized directly.
Immunoreactivity was visualized by electrochemiluminescence.
Fluorescence was visualized with ApoTome.
mCherry-ZmR1 was visualized.
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