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Recombinant Human mGluR5 Protein, CF

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Product Details

Summary
Reactivity HuSpecies Glossary
Format
Carrier-Free

Order Details

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Recombinant Human mGluR5 Protein, CF Summary

Details of Functionality
Bioassay data are not available.
Source
Mouse myeloma cell line, NS0-derived human mGluR5 protein
Ser19-Ser509, with a C-terminal 6-His tag
Accession #
N-terminal Sequence
Ser19
Structure / Form
Disuflide linked homodimer
Protein/Peptide Type
Innovator Recombinant Proteins
Purity
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Endotoxin Note
<0.10 EU per 1 μg of the protein by the LAL method.

Applications/Dilutions

Dilutions
  • Bioactivity not tested
Theoretical MW
56 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
SDS-PAGE
61-71 kDa, reducing conditions

Packaging, Storage & Formulations

Storage
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
  • 12 months from date of receipt, -20 to -70 °C as supplied.
  • 1 month, 2 to 8 °C under sterile conditions after reconstitution.
  • 3 months, -20 to -70 °C under sterile conditions after reconstitution.
Buffer
Lyophilized from a 0.2 μm filtered solution in PBS.
Purity
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Reconstitution Instructions
Reconstitute at 250 μg/mL in PBS.

Notes

This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.

Alternate Names for Recombinant Human mGluR5 Protein, CF

  • glutamate receptor, metabotropic 5
  • GPRC1E
  • GPRC1EMGLUR5metabotropic glutamate receptor 5
  • GRM5
  • mGlu5
  • mGluR5

Background

Metabotropic glutamate receptors (mGluRs) are coupled to effector systems through GTP-binding proteins and modulate glutamate neurotransmission in the central and peripheral nervous systems (1). Structurally, members from this family are characterized by a large N-terminal extracellular domain (ECD), seven transmembrane, and a cytoplasmic carboxyl-terminal domain variable in length. Two ECDs dimerize together and large conformational changes are induced when agonists bind to one or both domains (3). Intracellularly, a short C-terminus interacts directly with a G-protein (2). The receptors are subdivided into three groups (I-III) based on sequence homology, signal transduction and pharmacological properties (1). Group I includes mGluR1 and mGluR5. This group has been shown to activate phospholipase C and regulates neuronal ion channel activity. Human mGluR5 is 1212 amino acids (aa) in length. The 2-509 amino acids domain represents the ECD, with the apparent molecular mass approximately 64 kDa in SDS-PAGE under reducing conditions. Through its ECD, mGluR5 either homodimerizes or heterodimerizes with the Ca++ sensor receptor (4). Over aa 2-509, human mGluR5 is 98% aa identical to mouse and rat mGluR5.
  1. Conn PJ, et al. (1997) Annu Rev Pharmacol Toxicol 37:205.
  2. Pin JP, et al. (1995) Neuropharmacology. 34:1.
  3. Niswender CM, et al. (2010) Annu Rev Pharmacol Toxicol 50:295.
  4. Doré AS, et al. (2014) Nature 511:557.

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