Skip to Content
Merck
All Photos(4)

Documents

AB5511

Sigma-Aldrich

Anti-Opioid Receptor Antibody, µ, pain

serum, Chemicon®

Synonym(s):

mu opiate receptor, opioid receptor, mu 1

Sign Into View Organizational & Contract Pricing


About This Item

UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41

biological source

rabbit

Quality Level

antibody form

serum

antibody product type

primary antibodies

clone

polyclonal

species reactivity

mouse, primate, rat, human

manufacturer/tradename

Chemicon®

technique(s)

immunocytochemistry: suitable
immunohistochemistry: suitable
western blot: suitable

NCBI accession no.

UniProt accession no.

shipped in

dry ice

target post-translational modification

unmodified

Gene Information

human ... OPRM1(4988)

General description

Opiates derived from the opium poppy, Papaver somniferum, have been used for millenia for their anti-diarrheal, analgesic and euphoric properties. More recently, endogenous peptides, enkephalins, dynorphins, and endorphins, were found to bind to the same sites as opiate alkaloids. The receptors for the classical opioids are three related GPCRs, δ, κ, and µ (also known as OP1, OP2 and OP3, respectively), that activate Gi/o to reduce intracellular cAMP levels. Although most clinically used opioids function by activation of the µ opioid receptor, agonists of spinal δ opioid receptors have antinociceptive activity that is independent of µ. In addition, activation of δ increases locomotor activity, inhibits gastrointestinal motility, and decreases respiratory frequency (Dhawan et al., 1996). Agonists for δ opioid receptors also exhibit antidepressant-like activity in animal models (Broom et al., 2002).

Specificity

Mu Opioid receptor.
Other species have not been tested.

Immunogen

Epitope: C-terminus
Synthetic peptide from the C-terminus of rat Mu Opioid receptor.

Application

Detect Opioid Receptor using this Anti-Opioid Receptor Antibody, µ, pain validated for use in IC, IH & WB.
Immunohistochemistry:
1:2,500-1:5,000 dilution of a previous lot was used.

Western blot:
1:1,000 dilution of a previous lot was used.

Immunocytochemistry:
1:2,500-1:5,000 dilution of a previous lot was used.

Optimal working dilutions must be determined by the end user.
Research Category
Neuroscience
Research Sub Category
Neuroinflammation & Pain

Quality

Evaluated by Western Blot on Human Liver lysate.

Western Blot Analysis:
1:500 dilution of this antibody detected Opioid Receptor on 10 µg of Human Liver lysate.

Target description

45 kDa

Physical form

Rabbit polyclonal serum in buffer containing 0.05% sodium azide.
Unpurified

Storage and Stability

Stable for 1 year at -20ºC from date of receipt.

Analysis Note

Control
Spinal cord, liver lysate

Other Notes

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Legal Information

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

Not finding the right product?  

Try our Product Selector Tool.

Storage Class Code

10 - Combustible liquids

WGK

WGK 1


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Mu opioid receptors are expressed on radial glia but not migrating neuroblasts in the late embryonic mouse brain.
Tim J Sargeant,Darren J Day,Eli M Mrkusich,Darren F Foo,John H Miller
Brain Research null
Compartment-specific modulation of GABAergic synaptic transmission by mu-opioid receptor in the mouse striatum with green fluorescent protein-expressing dopamine islands.
Miura, M; Saino-Saito, S; Masuda, M; Kobayashi, K; Aosaki, T
The Journal of Neuroscience null
Sex differences in ?-opioid receptor expression in trigeminal ganglia under a myositis condition in rats.
Zhang, X; Zhang, Y; Asgar, J; Niu, KY; Lee, J; Lee, KS; Schneider, M; Ro, JY
European Journal of Pain null
Seung Keun Back et al.
Pain, 123(1-2), 117-126 (2006-03-28)
The present study investigated whether the loss of spinal mu-opioid receptors following peripheral nerve injury is related to mechanical allodynia. We compared the quantity of spinal mu-opioid receptor and the effect of its antagonists, such as naloxone and CTOP, on
Response of striosomal opioid signaling to dopamine depletion in 6-hydroxydopamine-lesioned rat model of Parkinson's disease: a potential compensatory role.
Koizumi, H; Morigaki, R; Okita, S; Nagahiro, S; Kaji, R; Nakagawa, M; Goto, S
Frontiers in Cellular Neuroscience null

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service