Recombinant Human mGluR2 Protein, CF Summary
Details of Functionality |
Bioassay data are not available. |
Source |
Mouse myeloma cell line, NS0-derived human mGluR2 protein Gly20-Ser498, with a C-terminal 6-His tag |
Accession # |
|
N-terminal Sequence |
Gly20 |
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 |
|
Theoretical MW |
54 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 |
60-75 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 and DTT. |
Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Reconstitution Instructions |
Reconstitute at 500 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 mGluR2 Protein, CF
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 domains, 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). The Group II receptors comprise
mGLuR2 and mGLuR3, which share high sequence homology. mGLuR2 is a presynaptic
receptor expressed on both neurons and glia, and its activation regulates cAMP
accumulation (1). Mature human mGluR2 is 854 amino acids in length, including a
549 amino acid (aa) N-terminal ECD. Within N-terminal ECD, human mGluR2 shares 98% aa sequence
identity with mouse and rat mGluR2.
-
Conn P.J. and Pin J.P. (1997) Annu. Rev. Pharmacol. Toxicol. 37:205.
- Pin J.P. and Duvoisin R. (1995) Neuropharmacology. 34:1.
- Niswender C.M. and Conn P.J. (2010) Annu. Rev. Pharmacol. Toxicol. 50:295.
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