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HTS160M Sigma-Aldrich

ChemiSCREEN Membrane Preparation Recombinant Human BB 3 Bombesin Receptor

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  •  eCl@ss 32161000

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Properties

Quality Level   100
biological source   human
recombinant   expressed in Chem-1 cells
mfr. no.   CHEMICON®
  ChemiScreen
application(s)   ligand binding assay: suitable (GTPγS)
  radioligand binding assay (RLBA): suitable
NCBI accession no.   NM_001727
UniProt accession no.   P32247

Description

General description

Bombesin, a bioactive peptide first identified in amphibian skin, is related to two mammalian peptides, gastrin-releasing peptide (GRP) and neuromedin B. A family of 3 GPCRs, including GRP-R (BB1), NMB-R (BB2) and BRS-3 (BB3), mediate the biological effects of the peptides (Ohki-Hamazaki et al., 2005). BB3 differs from the others by its low affinity for bombesin. Although an endogenous ligand for BB3 has yet to be identified, a synthetic nonselective bombesin-like peptide [H-D-Phe6, β-Ala11, Phe13, Nle14]-bombesin-(6-14)-nonapeptide amide (Bombesin (6-14) Analog) activates BB3 with high potency. BB3-null mice have an obese phenotype (Matsumoto and Iijima, 2003). Millipore′s BB3 membrane preparations are crude membrane preparations made from our proprietary stable recombinant cell lines to ensure high-level of GPCR surface expression; thus, they are ideal HTS tools for screening of antagonists of BB3 receptor interactions with its ligand. The membrane preparations exhibit a Kd of 0.23nM for [125I]-Bombesin (6-14) Analog. With 10 μg/well BB3 Membrane Prep and 0.3 nM [125I]-Bombesin (6-14) Analog, a greater than 3-fold signal-to-background ratio was obtained.

Full length human BRS3 encoding BB3

Application

Human BB3 GPCR membrane preparation for Radioligand binding Assays & GTPγS binding.

Radioligand binding assay and GTPγS binding

Biochem/physiol Actions

• GPCR Class: A
• Protein Target: BB3
• Target Sub-Family: Bombesin

Specifications

Membranes are mixed with radioactive ligand and unlabeled competitor (see Figures 1 and 2 for concentrations tested) in binding buffer in a nonbinding 96-well plate, and incubated for 1-2 h.Prior to filtration, an FC 96-well harvest plate (Millipore cat. # MAHF C1H) is coated with 0.33% polyethyleneimine for 30 min, then washed with 50mM HEPES, pH 7.4,0.5% BSA. Binding reaction is transferred to the filter plate, and washed 3 times (1 mL per well per wash) with Wash Buffer.The plate is dried and counted.

Binding buffer: 50 mM Hepes, pH 7.4, 5 mM MgCl2, 1 mM CaCl2, 0.2% BSA, 0.2 mg/ml bacitracin, 20 μg/ml leupeptin, 20 μg/ml chymostatin, 1 Protease Inhibitor cocktail Tablets (Roche Cat. No. 11 873 580 001) for each 50 ml binding buffer.

Radioligand: [125I]-Bombesin (6-14) Analog (Perkin Elmer NEX377)

Wash Buffer: 50 mM Hepes, pH 7.4, 500 mM NaCl , 0.1% BSA, filtered and stored at 4°C.

One package contains enough membranes for at least 200 assays (units), where an unit is the amount of membrane that will yield greater than 3-fold signal:background with 125I-labeled Bombesin (6-14) Analog at 0.3 nM.

Physical form

Liquid in packaging buffer: 50 mM Tris pH 7.4, 10% glycerol and 1% BSA with no preservatives.
Packaging method: Membranes protein was adjusted to the indicated concentration in packaging buffer, rapidly frozen, and stored at -80oC.

Storage and Stability

Maintain frozen at -70°C for up to 2 years. Do not freeze and thaw.

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

Safety & Documentation

Safety Information

WGK Germany 
WGK 2
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable
Protocols & Articles
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