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Cat. No.
Name
Size   
Price
Selected
M00406
1 vial
$320
Product Name Human ADRB2 Receptor Membrane Preparation
Species
Human
Documents
TECHNICAL MANUAL: 11655_20100104031418.PDF (PDF)
Document-EXAMPLE: 11659_20100104040407.JPG (JPG)
Document-EXAMPLE: 11660_20100104040441.JPG (JPG)
Figures
Reference
James A. (1984) ICI 118,551: an effective ocular hypotensive agent with selectivity for the ciliary process 132-adrenoceptor and with minimal cardiac side effects. Br. J. Pharmac. 83,821- 829.

Staehelin M, et. al. (1983) CGP-12177. A hydrophilic beta-adrenergic receptor radioligand reveals high affinity binding of agonists to intact cells. J. Biol. Chem. 258(6):3496-502.

Koike K. et. al. (1997) Characteristics of [3H]CGP12177 binding sites at beta 2- and beta 3-adrenoceptors in the guinea pig taenia caecum. Gen. Pharmacol. 28(1):73-6.

Description
β-Adrenergic receptors (β-ARs) are members of the superfamily G-protein-coupled receptors that are stimulated by naturally occurring catecholamines, epinephrine, and norepinephrine. As part of the sympathetic nervous system, β-ARs have been shown to have important roles in cardiovascular, respiratory, metabolic, central nervous system, and reproductive functions. Three distinct β-AR subtypes have been identified (β1-AR, β2-AR, and β3-AR). All three of these β-AR subtypes are believed to signal by coupling to the stimulatory G-protein Gsα which leads to the activation of adenylyl cyclase and accumulation of the second messenger cAMP. β1-ARs mediate cardiac stimulation, β2-ARs mediate smooth muscle relaxation in the peripheral vasculature and respiratory system, and β3-AR has been shown to have important roles in adipose tissue and gastrointestinal tract. In studies using subtype-selective agonists and antagonists in the human heart, β2-AR stimulation leads to the activation of adenylyl cyclase and contributes to both inotropic and chronotropic responses.
Host Cell
CHO-K1/ADRB2/Gα15
Concentration
1 mg/ml in 50 mM HEPES, 0.1 mM EDTA, 10 % glycerol
Storage
Store at -80°C
Quality Control
Bmax and Kd are determined using radioligand saturation binding assays (Figure 1).
Expression Level (Bmax): 31.1 pmol/mg membrane protein.
Kd for [3H]CGP-12177: 0.46 nM
Application
Binding assay for ADRAB2 receptor
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