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GFP fusion proteins were visualized by immunodetection.
After copper induction of the plasmid encoded MCA1454 and MCA1432 genes, total cell lysates were prepared and all Mca1 variants were visualized by immunodetection using polyclonal Mca1 antibodies.
Proteins were visualized by chemiluminescence using rabbit- or mouse-specific Western-SuperStar™ Immunodetection system (Applied Biosystems, Life Technologies, CA, USA).
Interactions were visualized by chemiluminescence.
Bands were visualized by chemiluminescence.
Immunoreactivity was visualized by electrochemiluminescence.
Cells were visualized by immunofluorescence.
The signals were visualized by PhosphorImager.
Phosphorylated histone bands were visualized by autoradiography.
Immunoreactive bands were visualized by chemiluminescence.
Protein-DNA complexes were visualized by phosphoimager.
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