Recombinant Human mGluR8 Protein, CF Summary
Details of Functionality |
Bioassay data are not available. |
Source |
Chinese Hamster Ovary cell line, CHO-derived human mGluR8 protein Gln34-Ser514, with a C-terminal 6-His tag |
Accession # |
|
N-terminal Sequence |
No results obtained. Gln34 inferred from enzymatic pyroglutamate treatment revealing Glu35 |
Structure / Form |
Disulfide 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 |
|
Theoretical MW |
55 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 |
54-70 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 mGluR8 Protein, CF
Background
Metabotropic
glutamate receptors (mGluRs) are members of the G-protein-coupled receptor
(GPCR) superfamily, modulating glutamate neurotransmission in the central and
peripheral nervous systems through GTP-binding proteins (1). Structurally,
members of this family are characterized by a large N-terminal extracellular
domain (ECD), seven transmembrane domains, and a cytoplasmic C-terminal domain that
is variable in length. Two ECDs dimerize together and large conformational
changes are induced when agonists bind to one or both domains (2). The C-terminal region is subject to
alternative splicing, regulation by phosphorylation, and interacts directly
with a G-protein to modulate protein-protein interactions (2, 3). The receptors
are subdivided into three groups (I–III) based on sequence homology, signal
transduction and pharmacological properties (1, 2). The Group III receptors
include mGLuRs 4, 6, 7 and 8 (2). Mature human mGluR8 is 875 amino acids in
length, including a 550 amino acid (aa) N-terminal ECD (4). Within N-terminal ECD, human
mGluR8 shares 98.4% and 98.5% aa sequence identity with mouse and rat mGluR8,
respectively.
-
Conn P.J. and Pin J.P. (1997) Annu. Rev. Pharmacol. Toxicol. 37:205.
- Niswender C.M. and Conn P.J. (2010) Annu. Rev. Pharmacol. Toxicol. 50: 295.
- Pin J.P. and Duvoisin R. (1995) Neuropharmacology. 34:1.
- Wu S. et al. (1998) Brain Res. Mol. Brain Res. 53:88.
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