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Purified Mouse Anti-Rat mGluR1α
Purified Mouse Anti-Rat mGluR1α
Western blot analysis of mGluR1α. Lysate from rat brain cells was probed with anti-mGluR1α at concentrations of 3.0 (lane 1), 1.0 (lane 2), and 0.5 µg/ml (lane 3). mGluR1µ is identified as a band of ~133 kDa.
Western blot analysis of mGluR1α. Lysate from rat brain cells was probed with anti-mGluR1α at concentrations of 3.0 (lane 1), 1.0 (lane 2), and 0.5 µg/ml (lane 3). mGluR1µ is identified as a band of ~133 kDa.
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BD Pharmingen™
Rat (QC Testing)
Mouse IgG1
Recombinant Rat mGluR1 Fusion Protein
Western blot (Routinely Tested), Immunohistochemistry-frozen (Tested During Development)
133 kDa
0.5 mg/ml
Aqueous buffered solution containing ≤0.09% sodium azide.


Applications include western blot analysis (1-2 µg/ml) and immunohistochemical staining of frozen tissue sections. Rat brain is suggested as a positive control for this application.


  1. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
  2. Please refer to for technical protocols.
  3. Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
556331 Rev. 8
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Glutamate is a major excitatory neurotransmitter in mammalian brain. Glutamatergic neurotransmission is mediated by a family of glutamate receptors that can be grouped into two classes, ionotropic (GluR) and metabotropic (mGluR) receptors. The metabotropic glutamate receptors consist of at least seven subtypes that can be divided into three groups on the basis of their sequence similarities, intracellular second messengers, and agonist selectivity's. These groups are 1) mGluR1 and mGluR5; 2) mGluR2 and mGluR3; and 3) mGluR4, mGluR6 and mGluR7. mGluR1 and mGluR5 are coupled to the inositol phosphate/Ca[2+] signal transduction pathway, whereas the other five receptors are linked to the inhibition of the cAMP cascade. mRNA analysis shows that the seven receptors have different expression patterns in the central nervous system. For example, the highest level of mGluR1 mRNA expression is found in the cerebellar Purkinje cells. mGluR7 mRNA is moderately expressed in these cells, whereas the mRNA of the other five mGluRs is barely detectable. Three splice variants have been described for mGluR1; mGluR1α (145 kDa), mGluR1β (97 kDa) and mGluR1c (97 kDa).

G209-488 recognizes rat mGluR1α. It does not cross-react with the other splice variants of mGluR1, mGluR1β and mGluR1c. Additionally G209-488 does not crossreact with mGluR5, the most closely related mGluR family member. The antibody was characterized by western blot analysis using rat brain membranes, and by immunohistochemical analysis using frozen rat brain tissue sections. A full length recombinant rat mGluR1 fusion protein was used as immunogen.  

556331 Rev. 8
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Tissue culture supernatant is purified by either protein A/G or affinity purification methods. Both methods yield antibody in solution that is free of most other soluble proteins, lipids, etc. This format provides pure antibody that is suitable for a number of downstream applications including: secondary labeling for flow cytometry or microscopy, ELISA, Western blot, etc.
556331 Rev.8
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研发参考 (3)

  1. Masu M, Tanabe Y, Tsuchida K, Shigemoto R, Nakanishi S. Sequence and expression of a metabotropic glutamate receptor. Nature. 1991; 349(6312):760-765. (Biology). 查看参考
  2. Shigemoto R, Abe T, Nomura S, Nakanishi S, Hirano T. Antibodies inactivating mGluR1 metabotropic glutamate receptor block long-term depression in cultured Purkinje cells. Neuron. 1994; 12(6):1245-1255. (Biology). 查看参考
  3. Shigemoto R, Nakanishi S, Mizuno N. Distribution of the mRNA for a metabotropic glutamate receptor (mGluR1) in the central nervous system: an in situ hybridization study in adult and developing rat. J Comp Neurol. 1992; 322(1):121-135. (Biology). 查看参考
556331 Rev. 8

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Global - Refer to manufacturer's instructions for use and related User Manuals and Technical data sheets before using this products as described

Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims.  Comparisons are not made against non-BD technologies, unless otherwise noted.

For Research Use Only. Not for use in diagnostic or therapeutic procedures.