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Mouse Anti-ADRB2 Recombinant Antibody (V2-606602) (CBMAB-X0259-FY)

This product is mouse antibody that recognizes ADRB2. The antibody CBFYA-0181 can be used for immunoassay techniques such as: FC, FuncS, Immunoassay.
See all ADRB2 antibodies

Summary

Host Animal
Mouse
Specificity
Human, Guinea pig, Rat
Clone
V2-606602
Antibody Isotype
IgG1
Application
IHC-F, FN, IA

Basic Information

Immunogen
Free peptide Beta2-H19C
Host Species
Mouse
Specificity
Human, Guinea pig, Rat
Antibody Isotype
IgG1
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.
ApplicationNote
FC1:50

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Buffer
PBS, 0.1% BSA
Preservative
None
Concentration
Batch dependent
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
Adrenoceptor Beta 2
Introduction
This gene encodes beta-2-adrenergic receptor which is a member of the G protein-coupled receptor superfamily. This receptor is directly associated with one of its ultimate effectors, the class C L-type calcium channel Ca(V)1.2. This receptor-channel complex also contains a G protein, an adenylyl cyclase, cAMP-dependent kinase, and the counterbalancing phosphatase, PP2A. The assembly of the signaling complex provides a mechanism that ensures specific and rapid signaling by this G protein-coupled receptor. This gene is intronless. Different polymorphic forms, point mutations, and/or downregulation of this gene are associated with nocturnal asthma, obesity and type 2 diabetes.
Entrez Gene ID
Human154
Guineapig
Rat24176
UniProt ID
HumanP07550
Guineapig
RatP10608
Alternative Names
Adrenoceptor Beta 2; Adrenergic, Beta-2-, Receptor, Surface; Beta-2 Adrenoreceptor; Beta-2 Adrenoceptor; ADRB2R; B2AR; Adrenoceptor Beta 2, Surface
Function
Beta-adrenergic receptors mediate the catecholamine-induced activation of adenylate cyclase through the action of G proteins. The beta-2-adrenergic receptor binds epinephrine with an approximately 30-fold greater affinity than it does norepinephrine.
Biological Process
Activation of adenylate cyclase activity
Activation of transmembrane receptor protein tyrosine kinase activity
Adenylate cyclase-activating adrenergic receptor signaling pathway
Adenylate cyclase-modulating G protein-coupled receptor signaling pathway
Adrenergic receptor signaling pathway
Bone resorption
Brown fat cell differentiation
Cell surface receptor signaling pathway
Cellular response to amyloid-beta
Desensitization of G protein-coupled receptor signaling pathway by arrestin
Diet induced thermogenesis
Endosome to lysosome transport
G protein-coupled receptor signaling pathway
Heat generation
Membrane organization
Negative regulation of inflammatory response to antigenic stimulus
Negative regulation of multicellular organism growth
Negative regulation of smooth muscle contraction
Norepinephrine-epinephrine-mediated vasodilation involved in regulation of systemic arterial blood pressure
Positive regulation of AMPA receptor activity
Positive regulation of autophagosome maturation
Positive regulation of bone mineralization
Positive regulation of cAMP-dependent protein kinase activity
Positive regulation of cold-induced thermogenesis
Positive regulation of lipophagy
Positive regulation of MAPK cascade
Positive regulation of mini excitatory postsynaptic potential
Positive regulation of protein kinase A signaling
Positive regulation of protein serine/threonine kinase activity
Positive regulation of transcription by RNA polymerase II
Protein deubiquitination
Receptor-mediated endocytosis
Regulation of sodium ion transport
Response to cold
Response to psychosocial stress
Cellular Location
Early endosome; Cell membrane; Golgi apparatus. Colocalizes with VHL at the cell membrane. Activated receptors are internalized into endosomes prior to their degradation in lysosomes. Activated receptors are also detected within the Golgi apparatus.
Topology
Extracellular: 1-34 aa
Helical: 35-58 aa
Cytoplasmic: 59-71 aa
Helical: 72-95 aa
Extracellular: 96-106 aa
Helical: 107-129 aa
Cytoplasmic: 130-150 aa
Helical: 151-174 aa
Extracellular: 175-196 aa
Helical: 197-220 aa
Cytoplasmic: 221-274 aa
Helical: 275-298 aa
Extracellular: 299-305 aa
Helical: 306-329 aa
Cytoplasmic: 330-413 aa
PTM
Palmitoylated. Mainly palmitoylated at Cys-341. Palmitoylation may reduce accessibility of phosphorylation sites by anchoring the receptor to the plasma membrane. Agonist stimulation promotes depalmitoylation and further allows Ser-345 and Ser-346 phosphorylation. Also undergoes transient, ligand-induced palmitoylation at Cys-265 probably by ZDHHC9, ZDHHC14 and ZDHHC18 within the Golgi. Palmitoylation at Cys-265 requires phosphorylation by PKA and receptor internalization and stabilizes the receptor. Could be depalmitoylated by LYPLA1 at the plasma membrane.
Phosphorylated by PKA and BARK upon agonist stimulation, which mediates homologous desensitization of the receptor. PKA-mediated phosphorylation seems to facilitate phosphorylation by BARK.
Phosphorylation of Tyr-141 is induced by insulin and leads to supersensitization of the receptor.
Polyubiquitinated. Agonist-induced ubiquitination leads to sort internalized receptors to the lysosomes for degradation. Deubiquitination by USP20 and USP33, leads to ADRB2 recycling and resensitization after prolonged agonist stimulation. USP20 and USP33 are constitutively associated and are dissociated immediately after agonist stimulation. Ubiquitination by the VHL-E3 ligase complex is oxygen-dependent.
Hydroxylation by EGLN3 oCcurs only under normoxia and increases the interaction with VHL and the subsequent ubiquitination and degradation of ADRB2.

Hikino, K., Kobayashi, S., Ota, E., Mushiroda, T., Urayama, K. Y., & Kobayashi, T. (2021). A meta‐analysis of the influence of ADRB2 genetic polymorphisms on albuterol (salbutamol) therapy in patients with asthma. British Journal of Clinical Pharmacology, 87(4), 1708-1716.

Wang, Y., & Jiang, S. (2021). The role of ADRB2 gene polymorphisms in malignancies. Molecular Biology Reports, 1-9.

Lehrer, S., & Rheinstein, P. H. (2020). The ADRB1 (Adrenoceptor Beta 1) and ADRB2 Genes Significantly Co-express with Commonly Mutated Genes in Prostate Cancer. Discovery medicine, 30(161), 163.

Karimi, L., Lahousse, L., Ghanbari, M., Terzikhan, N., Uitterlinden, A. G., van der Lei, J., ... & Verhamme, K. (2019). β2-Adrenergic Receptor (ADRB2) Gene Polymorphisms and Risk of COPD Exacerbations: The Rotterdam Study. Journal of clinical medicine, 8(11), 1835.

Toraih, E. A., Hussein, M. H., Ibrahim, A., AbdAllah, N. B., Mohammad, E., Kishk, A. M., & Fawzy, M. S. (2019). Beta2-adrenergic receptor variants in children and adolescents with bronchial asthma. Front Biosci (Elite Ed), 11, 61-78.

Wang, L., Lv, Q., Song, X., Jiang, K., & Zhang, J. (2019). ADRB2 suppresses IL-13-induced allergic rhinitis inflammatory cytokine regulated by miR-15a-5p. Human cell, 32(3), 306-315.

Zhang, X., Zhang, Y., He, Z., Yin, K., Li, B., Zhang, L., & Xu, Z. (2019). Chronic stress promotes gastric cancer progression and metastasis: An essential role for ADRB2. Cell death & disease, 10(11), 1-15.

Ágg, B., Baranyai, T., Makkos, A., Vető, B., Faragó, N., Zvara, Á., ... & Ferdinandy, P. (2018). MicroRNA interactome analysis predicts post-transcriptional regulation of ADRB2 and PPP3R1 in the hypercholesterolemic myocardium. Scientific reports, 8(1), 1-11.

Wang, X., Li, Q., Liu, R., He, J., Wu, D., Wang, Y., & Zhang, J. (2018). ADRB2 Arg16Gly polymorphism and pulmonary function response of inhaled corticosteroids plus long-acting beta agonists for Asthma treatment: A systematic review and meta-analysis. Canadian respiratory journal, 2018.

Nielsen, A. O., Jensen, C. S., Arredouani, M. S., Dahl, R., & Dahl, M. (2017). Variants of the ADRB2 gene in COPD: systematic review and meta-analyses of disease risk and treatment response. COPD: Journal of Chronic Obstructive Pulmonary Disease, 14(4), 451-460.

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For research use only. Not intended for any clinical use.

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