Loading...
Products:Neuroscience >> Neurotransmission >> Receptors / Channels >> GPCR >> Cannabinoid Receptor
If your product does not perform as described on this datasheet, we will refund or replace your product...
Read our guarantee »Anti-Cannabinoid Receptor II antibody
See all Cannabinoid Receptor II products (6) ...
Rabbit polyclonal to Cannabinoid Receptor II
Detects CB2 from human and rat tissues as well as transfected rat CB2. Immunocytochemical staining of CB2 on AtT20 cells transfected with the rat CB2 gene yields a pattern consistent with plasma membrane staining.
IHC-Fr, WB, IHC-P, ICC, ICC/IF, Flow Cytmore details
Reacts with
Mouse, Rat, Human, Chinese Hamster
Fusion protein, corresponding to amino acids 1-32 of Rat Cannabinoid Receptor II.
AtT20 cells.
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
PBS, 50% glycerol, 1 mg/ml BSA and 0.05% sodium azide
Concentration information loading...
Immunogen affinity purified
Cannabinoids exert their well known physiological effects through two G protein coupled receptors, cannabinoid receptor 1 (CB1) and CB2. Both cannabinoid receptors have been shown to inhibit adenylyl cyclase as well as stimulate the mitogen-activated protein kinase, MAPK. CB1 receptors also modulate ion channels through direct G-protein interactions. Delta 9-tetrahydrocannibinol and related ligands likely exert their psychoactive effects by inhibiting presynaptic N- and P / Q type calcium channels. CB2 is thought to function primarily in the immune system although it has been suggested to be present in the central nervous system, including the retina.
Polyclonal
IgG
Neuroscience >> Neurotransmission >> Receptors / Channels >> GPCR >> Cannabinoid Receptor
Our Abpromise guarantee covers the use of ab3561 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Flow Cyt: Use at an assay dependent dilution (PMID 18178718).
ICC/IF: 1/500 - 1/5000.
IHC-P: Use at an assay dependent concentration.
IHC-Fr: 1/500.
WB: Use at an assay dependent dilution. Predicted molecular weight: 40 kDa.
Not yet tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.
Heterotrimeric G protein-coupled receptor for endocannabinoid 2-arachidonoylglycerol mediating inhibition of adenylate cyclase. May function in inflammatory response, nociceptive transmission and bone homeostasis.
Preferentially expressed in cells of the immune system with higher expression in B cells and NK cells (at protein level). Expressed in skin in suprabasal layers and hair follicles (at protein level). Highly expressed in tonsil and to a lower extent in spleen, peripheral blood mononuclear cells, and thymus. PubMed:14657172 could not detect expression in normal brain. Expressed in brain by perivascular microglial cells and dorsal root glanglion sensory neurons (at protein level).
Belongs to the G-protein coupled receptor 1 family.
Constitutively phosphorylated on Ser-352; phosphorylation increases cell internalization and desensitizes the receptor.
Cell membrane. Cell projection > dendrite. Perikaryon. Localizes to apical dendrite of pyramidal neurons.
Target information above from: UniProt accessionP34972
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Cannabinoid Receptor II antibody (ab3561)

ab3561 at 1/5000 staining rat spinal cord tissue sections by IHC-P. Following nerve trans-section, the animal was transcardially perfused with PBS followed by 4% formaldehyde (no post fixation) then frozen in OCT and stored at -80°C until required. 20µm sections were cut and stained with the antibody for 18 hours. A biotinylated goat anti-rabbit antibody was used as the secondary.
This image is courtesy of an Abreview submitted by Ms Nancy Nutile-McMenemy
Immunocytochemistry/ Immunofluorescence - Cannabinoid Receptor II antibody (ab3561)

ab3561 staining Cannabinoid Receptor II in murine BV2 cells by Immunocytochemistry/ Immunofluorescence. Cells were stimulated with 10 uM ADP for 15 minutes at 37°C, 5%CO2 then washed 3X with PBS and fixed with 2% formaldehyde for 15 minutes at room temperature. A blocking step was performed for 1 hour at room temperature with 5% FBS/PBS/0.01% Triton-X-100. ab3561 used at a 1/500 dilution for 1 hour at room temperature then washed 3X PBS. The secondary was an Alexa Fluor 488 conjugated antibody, used at a 1/250 for 1 hour at room temperature, washed 3X PBS then mounted in Vectashield containing DAPI.
Image courtesy of an anonymous Abreview.
Flow Cytometry - Anti-Cannabinoid Receptor II antibody (ab3561)

Quantification of Cannabinoid Receptor II surface expression in primary human and HaCaT keratinocytes. FL-1 shows autofluorescence (black population), non-specific binding of secondary antibody (dark grey population) and specific immunofluorescence obtained with ab3561, respectively (light grey population).
Image from Leonti M et al, Biochem Pharmacol. 2010 Jun 15;79(12):1815-26. Epub 2010 Mar 3, Fig 6. DOI 10.1016/j.bcp.2010.02.015
This product has been referenced in:
See all 11 publications for this product
Publishing research using ab3561? Please let us know so that we can cite the reference in this datasheet
Concentration of lot no. is
Concentration not available for this lot.
Find concentration of your lot:

ab3561 at 1/5000 staining rat spinal cord tissue sections by IHC-P. Following nerve trans-section, the animal was transcardially perfused with PBS followed by 4% formaldehyde (no post fixation) then frozen in OCT and stored at -80°C until required. 20µm sections were cut and stained with the antibody for 18 hours. A biotinylated goat anti-rabbit antibody was used as the secondary.
This image is courtesy of an Abreview submitted by Ms Nancy Nutile-McMenemy

ab3561 staining Cannabinoid Receptor II in murine BV2 cells by Immunocytochemistry/ Immunofluorescence. Cells were stimulated with 10 uM ADP for 15 minutes at 37°C, 5%CO2 then washed 3X with PBS and fixed with 2% formaldehyde for 15 minutes at room temperature. A blocking step was performed for 1 hour at room temperature with 5% FBS/PBS/0.01% Triton-X-100. ab3561 used at a 1/500 dilution for 1 hour at room temperature then washed 3X PBS. The secondary was an Alexa Fluor 488 conjugated antibody, used at a 1/250 for 1 hour at room temperature, washed 3X PBS then mounted in Vectashield containing DAPI.
Image courtesy of an anonymous Abreview.

Quantification of Cannabinoid Receptor II surface expression in primary human and HaCaT keratinocytes. FL-1 shows autofluorescence (black population), non-specific binding of secondary antibody (dark grey population) and specific immunofluorescence obtained with ab3561, respectively (light grey population).
Image from Leonti M et al, Biochem Pharmacol. 2010 Jun 15;79(12):1815-26. Epub 2010 Mar 3, Fig 6. DOI 10.1016/j.bcp.2010.02.015

12
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
Call 01223 696 000 or contact us
