Skip header information|
Wadsworth Center Home - Science in the Pursuit of Health|
Main Body

Advanced Light Microscopy and Image Analysis Core

Time-line of imaging technology: phase contrast, differential interference,
microinjected fluorescence anti-tubulin antibody, GFP tagged Histone, fixed
preparation labeling three different proteins using antibodies/dye (DNA
blue, actin red, microtubules green).
Timeline of imaging technology

Imaging

What do you need to image? Click link(s) below to see how we can help.

Tissue (100-1000X)

Most fluorescently labeled tissues slices (100µm uncleared and up to 500µm cleared) are best imaged with a confocal microscope. The confocal microscope removes most of the "out-of-focus" blur associated with imaging fluorescent specimens that are thicker than the depth of field of the objective lens.

Multi-channel:
* up to 3 biomolecules/fluorophore can be collected simultaneously examples in gallery + reflection microscopy

*Z series (can be combined with multi biomolecules or fluorophores)

Cells (100-1000X)

Live (RT ->500C)
Transmitted light:

Fluorescence: Metal halide illumination

Fixed (fluorescent or histological stains)
Multi-channel:

True color:

Whole mounts

Confocal: object(s) <500uM

Dissecting scope: object(s) 300µM to mm's

Other

Opaque objects: small parts, tobacco, etc.

Phase objects: Crystals