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Mini-Review

Over the Rainbow: 25 Years of Confocal Imaging

Pages 643-648 | Published online: 16 May 2018

Figures & data

Figure 1. Development of multiple label confocal imaging from the 1980s to the present.

(A)–(C). Confocal imaging in the 1980s. (A) Wide-field epifluorescence image of a 3T3 cell immunofluorescently labeled with antitubulin. (B) Laser scanning confocal image of similar cell. (C) Double label confocal image of the same cell in (B); tubulin in green and nuclei labeled with propidium iodide in red. (D) Confocal imaging in the 1990s. Single optical sections collected simultaneously using a single krypton argon laser at three different excitation wavelengths—488 nm, 568 nm, and 647 nm—of a fruit fly third instar wing imaginal disk labeled for three genes involved with patterning the wing: cubitus interruptus (fluorescein, 496 nm) in green; vestigial (lissamine rhodamine, 572 nm) in red; and apterous (cyanine 5, 649 nm) in blue. (E) Confocal imaging in the 21st century. Brainbow image of mouse dentate gyrus (Citation21).

Figure 1. Development of multiple label confocal imaging from the 1980s to the present.(A)–(C). Confocal imaging in the 1980s. (A) Wide-field epifluorescence image of a 3T3 cell immunofluorescently labeled with antitubulin. (B) Laser scanning confocal image of similar cell. (C) Double label confocal image of the same cell in (B); tubulin in green and nuclei labeled with propidium iodide in red. (D) Confocal imaging in the 1990s. Single optical sections collected simultaneously using a single krypton argon laser at three different excitation wavelengths—488 nm, 568 nm, and 647 nm—of a fruit fly third instar wing imaginal disk labeled for three genes involved with patterning the wing: cubitus interruptus (fluorescein, 496 nm) in green; vestigial (lissamine rhodamine, 572 nm) in red; and apterous (cyanine 5, 649 nm) in blue. (E) Confocal imaging in the 21st century. Brainbow image of mouse dentate gyrus (Citation21).