Showing posts with label Vanilloid Receptor Antibody. Show all posts
Showing posts with label Vanilloid Receptor Antibody. Show all posts

Saturday, August 05, 2017

Pain and Inflammation Markers

Our TRPV1 Markers Rock
As sales of our Cell Based Assay Solutions continue to explode. We don't want you to forget that our roots firmly remain in products for Inflammation and Pain Researchers.

To verify this, you only need to check out the many publications referencing use of our TRPV1 Markers.

Image: Immunoreactivity for CXCL12 was detected in the macrophages (F4/80)

Friday, May 19, 2017

TRPV1 Channels and Neuropathic Pain

Neuromics' TRPV1 Stain Neurons and Microglia for Study

TRPV1 is mainly functional in the microglia. Its activation, beyond controlling microglia reaction per se, modulated microglia-neuron communication, by promoting release of extracellular vesicles (EVs) from microglia. Indeed, EVs are important mediators of intercellular communication between microglia and brain cells: Maria Cristina Marrone, Annunziato Morabito, Michela Giustizieri, Valerio Chiurchiù, Alessandro Leuti, Marzia Mattioli, Sara Marinelli, Loredana Riganti, Marta Lombardi, Emanuele Murana, Antonio Totaro, Daniele Piomelli, Davide Ragozzino, Sergio Oddi, Mauro Maccarrone, Claudia Verderio & Silvia Marinelli. TRPV1 channels are critical brain inflammation detectors and neuropathic pain biomarkers in mice. Nature Communications 8, Article number: 15292 (2017) doi:10.1038/ncomms15292.

(a–f) Sections of cortical tissue from WT and TRPV1−/− mice, fixed after exposure to ACSF (a,d), ACSF plus vehicle (DMSO; b,e) and ACSF plus 1μM capsaicin (c,f) and immune-processed for iba-1 to stain microglia cells (in red). INSETs are zoom images taken from an area delimited by the yellow square for each condition. (g), Bar graph of percentage of cortical microglia cell phenotype (resting, ameboid, bushy and hypertrophied), in control (grey bars), vehicle- (dark grey bars) and capsaicin- treated (red bars) cortical sections from WT mice. Capsaicin treatment causes a significant shift from ramified and bushy to hypertrophied morphology. (h), Same as in ‘g’ but in cortical sections from TRPV1−/− mice. In these tissues capsaicin fails to induce morphological changes of microglia cells. Note that microglia cells in −/− tissues are already hypertrophied in control conditions (d–f,h).
Our Pain and Inflammation Research Antibodies Continue to be widely used and frequently published.