Licensing

Pd
Public Domain: This image is in the public domain and thus free of any copyright restrictions. However, as is the norm in scientific publishing and as a matter of courtesy, any user should credit the content provider for any public or private use of this image whenever possible. Learn more
Comments: Powered by Pnyxe

Description

Dorsal root ganglion cells from embryonic mice were cultured and stimulated to produce cyclooxygenase-2 (COX-2). Cultures were immuno-stained for neuron-associated tubulin (green), COX-2 (red) and DNA (blue). COX-2 is primarily expressed in neurons.

Technical Details

After induction of COX-2, cultures were fixed with paraformaldehyde overnight, then immunostained with a mouse antibody to neuronal class III beta-tubulin followed by an Alexa 488-conjugated goat anti-mouse to identify neurons. COX-2 was imaged using Fluorocoxib A, a selected COX-2 inhibitor conjugated to carboxy-X-rhodamine (see http://cancerres.aacrjournals.org/content/70/9/3618.full). Preparations were counterstained with DAPI, and imaged with a Leica CMS microscope using a 40x 0.8 NA objective lens. Images were recorded with a Qimaging Qi CCD camera.

Biological Sources

NCBI Organism Classification
Mus musculus
(house mouse)
Cell Type
dorsal root ganglion
neuron of the dorsal spinal cord

Attribution

Names
Kelsey C Duggan
Daniel J Hermanson
Joel Musee
Jeffery J Prusiakiewicz
Jami L Scheib
Bruce D Carter
Surajit Banerjee
J A Oates
Lawrence J Marnett
Published
NIGMS Biomedial Beat
K C Duggan et al. 2011 (R)-Profens are substrate-selective inhibitors of endocannabinoid oxygenation by COX-2 Nat
Link
NIGMS Biomedical Beat
Pubmed
22053353

Sample Preparation

Methods
formaldehyde fixed tissue
Relation To Intact Cell
whole mounted tissue

Dimensions

Spatial Axis Image Size Pixel Size
X 1392px 0.24μm
Y 1040px 0.24μm
*CIL – Cell Image Library accession number. Please use this to reference an image.