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Human ADRB2 Reporter Assay Kit

SIZE SKU PRICE
1 x-384 well format assays
1 x-96 well format assays
SIZE SKU
1 x-384 well format assays
1 x-96 well format assays

Product Description and Product Data

This is an all-inclusive cell-based luciferase reporter assay kit targeting the the Human Adrenoreceptor Beta 2 (ADRB2). INDIGO’s ADRB2 reporter assay utilizes proprietary mammalian cells that have been engineered to provide constitutive expression of the ADRB2. In addition to ADRB2 Reporter Cells, this kit provides two optimized media for use during cell culture and in diluting the user’s test samples, a reference agonist, Luciferase Detection Reagent, and a cell culture-ready assay plate. The principal application of this assay is in the screening of test samples to quantify any functional activity, either agonist or antagonist, that they may exert against ADRB2. This kit provides researchers with clear, reproducible results, exceptional cell viability post-thaw, and consistent results lot to lot. Kits must be stored at -80C. Do not store in liquid nitrogen. Note: reporter cells cannot be refrozen or maintained in extended culture.

Features

  • Clear, Reproducible Results

  • All-Inclusive Assay Systems
  • Exceptional Cell Viability Post-Thaw
  • Consistent Results Lot to Lot

Product Specifications

Target TypeGPCR
SpeciesHuman
Receptor FormHybrid
Assay ModeAgonist, Antagonist
Kit Components
  • Human ADRB2 Reporter Cells
  • Cell Recovery Medium (CRM)
  • Compound Screening Medium (CSM)
  • Isoproterenol, (ref. agonist; in DMSO)
  • Detection Substrate
  • Detection Buffer
  • White, sterile, cell-culture ready assay plate
Shelf Life6 months
Shipping RequirementsDry Ice
Storage temperature-80C

Data

Activation of ADRB2. Activation assays were performed using the reference compounds Isoproterenol (provided), Salbutamol, Epinephrine, Norepinephrine and Denopamine. Luminescence was quantified and values of average (n = 3) relative light units (RLU), corresponding standard deviation (SD), Fold-Activation, and Z’ values were calculated. The least-squares method of non-linear regression was used to plot Fold-Activation or RLU vs. Log10 [Compound, nM] and EC50 / IC50 values were determined using GraphPad Prism software. All chemicals were procured from Cayman Chemical, Ann Arbor MI, USA.
Inhibition of ADRB2. ADRB2 reporter cells were co-treated with an EC80 concentration of the reference activator Isoproterenol and varying concentrations of the ADRB2 inhibitors ICI 118551, Timolol and Propanolol. INDIGO’s Live Cell Multiplex (LCM) Assay confirmed that no treatment concentrations were cytotoxic (data not shown). Luminescence was quantified and values of average (n = 3) relative light units (RLU), corresponding standard deviation (SD), Fold-Activation, and Z’ values were calculated. The least-squares method of non-linear regression was used to plot Fold-Activation or RLU vs. Log10 [Compound, nM] and EC50 / IC50 values were determined using GraphPad Prism software. All chemicals were procured from Cayman Chemical, Ann Arbor MI, USA.

Target Background

The adrenoreceptors (a.k.a. adrenergic receptors) mediate the action of the sympathetic nervous system and are activated in response to “fight-or-flight” signals. They are divided into three types, adrenoreceptor α1-, α2-, and β. Each type is further composed of three subtypes resulting in 9 different types (α1A, α1B, α1D, α2A, α2B, α2C, β1, β2, and β3).

Adrenoreceptors belong to the G-Protein-coupled receptor (GPCR) family. They all display the characteristic seven transmembrane helices, the extracellular loops which contribute to ligand binding, and the intracellular carboxy tail that associates with trimeric G proteins. All nine types of adrenoreceptors are activated by the same endogenous catecholamines (epinephrine and norepinephrine); however, the specificity of their responses depends on the G-proteins and effectors systems they associate with in a tissue and time specific manner.

The beta-2 adrenoceptor (ADRB2) is abundantly expressed in the bronchial smooth muscle cells and activation of the receptor leads to bronchodilation. In addition, ADRB2 is expressed in cardiac myocytes and vascular smooth muscle cells. Receptor stimulation is known to be a primary control point for the modulation of heart rate and myocardial contractility. Upon binding to ligands, ADRB2 undergoes a conformational change that triggers the activation of Gs proteins via an exchange of GDP with GTP, followed by the activation of adenylate cyclase and the production of the second messenger cAMP.

ADRB2 is the target of clinically important drugs for asthma and cardiovascular conditions including hypertension and congestive heart failure (CHF). Various substances, including many medications, can be used to manipulate ADRB2. For example, Beta-agonists like Salbutamol and antagonists like Propranolol are among the most prescribed medications in the treatment of asthma and cardiovascular disease, respectively. Consequently, the ADRB2 receptor commands considerable interest in therapeutics development and drug safety screening.

Also available as a service

Adrenoreceptor Beta 2 (ADRB2)

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