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Immunofluorescence with mouse anti-alpha-tubulin was employed to visualize distribution of the microtubule network in a log phase monolayer culture of opossum kidney cells. The secondary antibody (goat anti-mouse IgG) was conjugated to Alexa Fluor 546 and mixed with Alexa Fluor 488 conjugated to phalloidin to simultaneously image tubulin and the actin cytoskeleton.
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