Rabbit Recombinant Monoclonal GRM1 antibody. Carrier free. Suitable for IHC-Fr, IP, WB, IHC-P and reacts with Rat, Mouse samples.
pH: 7.2 - 7.4
Constituents: 100% PBS
IHC-Fr | IP | WB | IHC-P | |
---|---|---|---|---|
Human | Not recommended | Not recommended | Not recommended | Not recommended |
Mouse | Tested | Tested | Tested | Tested |
Rat | Tested | Tested | Tested | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Rat, Mouse | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info - | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species Rat | Dilution info - | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
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G-protein coupled receptor for glutamate. Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the activity of down-stream effectors. Signaling activates a phosphatidylinositol-calcium second messenger system. May participate in the central action of glutamate in the CNS, such as long-term potentiation in the hippocampus and long-term depression in the cerebellum (By. similarity). May function in the light response in the retina (PubMed:26427409). Induces GRID1 and GRID2 cation-channel activation via GNAQ-PLC-PKC pathway in dopaminergic neurons and cerebellar Purkinje cell, respectively (PubMed:24357660, PubMed:27276689, PubMed:28696429).
Gprc1a, Mglur1, Grm1, Metabotropic glutamate receptor 1, mGluR1
Rabbit Recombinant Monoclonal GRM1 antibody. Carrier free. Suitable for IHC-Fr, IP, WB, IHC-P and reacts with Rat, Mouse samples.
pH: 7.2 - 7.4
Constituents: 100% PBS
ab289639 is the carrier free version of Anti-mGluR1a antibody [EPR24160-173] ab259888
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.
This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
MGluR1a also known as metabotropic glutamate receptor 1a is a G-protein coupled receptor with a mass of approximately 153 kDa. This receptor binds glutamate an excitatory neurotransmitter and initiates intracellular signaling by activating G-proteins. It is expressed in various regions of the brain such as the cerebellum hippocampus and olfactory bulb. The receptor is involved in modulating several synaptic processes by influencing the release of neurotransmitters.
Glutamate receptor mGluR1a plays a significant role in neuroplasticity and synaptic transmission. It does not act alone but is part of a larger group of metabotropic glutamate receptors. These receptors participate in both excitatory and inhibitory signaling pathways affecting signal regulation and neuron connectivity. mGluR1a contributes to learning and memory processes through its ability to modulate synaptic strength.
MGluR1a is an important component in the phosphatidylinositol signaling system and the glutamatergic synapse pathway. Both pathways are related to calcium ion homeostasis and protein trafficking in neurons. Among the related proteins Homer and Shank play a role in the mGluR1a signaling complex and aid in its function within these pathways affecting synaptic structure and plasticity.
MGluR1a is associated with several neuropathological conditions. Alterations in its function or expression can contribute to the development of neurodegenerative diseases like Alzheimer’s disease and psychiatric disorders such as schizophrenia. The receptor interacts with proteins like amyloid precursor protein (APP) and SynGAP which play roles in the etiology and progression of these conditions. Dysregulation of mGluR1a signaling may affect neuronal death and lead to cognitive defects seen in these diseases.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
This data was developed using Anti-mGluR1a antibody [EPR24160-173] ab259888, the same antibody clone in a different buffer formulation.
mGluR1a was immunoprecipated from mouse cerebellum tissue lysate 10 μg with Anti-mGluR1a antibody [EPR24160-173] ab259888 at 1/30 dilution. Western blot was performed on the immunoprecipitate using Anti-mGluR1a antibody [EPR24160-173] ab259888 at 1/1000 dilution. VeriBlot for IP secondary antibody (HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/5000 dilution.
Lane 1: (Input) Mouse cerebellum tissue lysate 10 μg
Lane 2: Mouse cerebellum tissue lysate
Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-mGluR1a antibody [EPR24160-173] ab259888 in mouse cerebellum tissue lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
The expression profile is consistent with the literature. PMID: 27721389.
All lanes: Immunoprecipitation - Anti-mGluR1a antibody [EPR24160-173] - BSA and Azide free (ab289639)
Predicted band size: 132 kDa
Observed band size: 101 kDa, 132 kDa, 260 kDa
This data was developed using Anti-mGluR1a antibody [EPR24160-173] ab259888, the same antibody clone in a different buffer formulation.
5% NFDM/TBST was used as a blocking and diluting buffer.
Samples are non-boiled as boiling may cause protein aggregates.
Low expression: pinnae (PMID: 18776920)
The expression profile is consistent with the literature: PMID: 27721389.
All lanes: Western blot - Anti-mGluR1a antibody [EPR24160-173] - BSA and Azide free (ab289639) at 1/1000 dilution
Lane 1: Mouse brain tissue lysate at 20 µg
Lane 2: Mouse cerebellum tissue lysate at 20 µg
Lane 3: Mouse pinnae tissue lysate at 20 µg
Lane 4: Rat brain tissue lysate at 20 µg
Lane 5: Rat cerebellum tissue lysate at 20 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/100000 dilution
Predicted band size: 132 kDa
Observed band size: 132 kDa, 260 kDa
Exposure time: 3min
This data was developed using Anti-mGluR1a antibody [EPR24160-173] ab259888, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse cerebellum labelling mGluR1a with Anti-mGluR1a antibody [EPR24160-173] ab259888 at 1/2000(0.261ug/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Cytoplasmic staining on mouse cerebellum (PMID: 30190524). The section was incubated with Anti-mGluR1a antibody [EPR24160-173] ab259888 (1/2000) for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
This data was developed using Anti-mGluR1a antibody [EPR24160-173] ab259888, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse kidney labelling mGluR1a with Anti-mGluR1a antibody [EPR24160-173] ab259888 at 1/2000(0.261ug/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Apical staining on mouse kidney. The section was incubated with Anti-mGluR1a antibody [EPR24160-173] ab259888 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
This data was developed using Anti-mGluR1a antibody [EPR24160-173] ab259888, the same antibody clone in a different buffer formulation.
mGluR1a was immunoprecipated from rat cerebellum tissue lysate 10 μg with Anti-mGluR1a antibody [EPR24160-173] ab259888 at 1/30 dilution. Western blot was performed on the immunoprecipitate using Anti-mGluR1a antibody [EPR24160-173] ab259888 at 1/1000 dilution. VeriBlot for IP secondary antibody (HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/5000 dilution.
Lane 1: (Input) Rat cerebellum tissue lysate 10 μg
Lane 2: Rat cerebellum tissue lysate
Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-mGluR1a antibody [EPR24160-173] ab259888 in rat cerebellum tissue lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
The expression profile is consistent with the literature. PMID: 27721389.
All lanes: Immunoprecipitation - Anti-mGluR1a antibody [EPR24160-173] - BSA and Azide free (ab289639)
Predicted band size: 132 kDa
Observed band size: 101 kDa, 132 kDa
This data was developed using Anti-mGluR1a antibody [EPR24160-173] ab259888, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat cerebellum labelling mGluR1a with Anti-mGluR1a antibody [EPR24160-173] ab259888 at 1/2000(0.261ug/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Cytoplasmic staining on rat cerebellum. The section was incubated with Anti-mGluR1a antibody [EPR24160-173] ab259888 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
This data was developed using Anti-mGluR1a antibody [EPR24160-173] ab259888, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat kidney labelling mGluR1a with Anti-mGluR1a antibody [EPR24160-173] ab259888 at 1/2000(0.261ug/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Apical staining on rat kidney. The section was incubated with Anti-mGluR1a antibody [EPR24160-173] ab259888 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
Immunohistochemical analysis of 4% PFA-fixed frozen mouse cerebellum (fresh) tissue labelling mGluR1a with Anti-mGluR1a antibody [EPR24160-173] ab259888 at 1/500 dilution (0.98 μg/ml) followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 at 1/1000 dilution (2 μg/mL). Positive staining on mouse cerebellum is observed.
Secondary antibody control: Secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 at 1/1000 dilution (2 μg/mL).
This data was developed using Anti-mGluR1a antibody [EPR24160-173] ab259888, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed frozen rat cerebellum (fresh) tissue labelling mGluR1a with Anti-mGluR1a antibody [EPR24160-173] ab259888 at 1/500 dilution (0.98 μg/ml) followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 at 1/1000 dilution (2 μg/mL). Positive staining on rat cerebellum is observed.
Secondary antibody control: Secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 at 1/1000 dilution (2 μg/mL).
This data was developed using Anti-mGluR1a antibody [EPR24160-173] ab259888, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed frozen mouse pinnae (fresh) tissue labelling mGluR1a with Anti-mGluR1a antibody [EPR24160-173] ab259888 at 1/500 dilution (0.98 μg/ml) followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 at 1/1000 dilution (2 μg/mL). Negative control: no staining on mouse pinnae (PMID: 18776920) is observed.
Secondary antibody control: Secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 at 1/1000 dilution (2 μg/mL).
This data was developed using Anti-mGluR1a antibody [EPR24160-173] ab259888, the same antibody clone in a different buffer formulation.
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