Anti-mGluR1a antibody [EPR24160-173] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal GRM1 antibody. Carrier free. Suitable for IHC-Fr, IP, WB, IHC-P and reacts with Rat, Mouse samples.
View Alternative Names
Gprc1a, Mglur1, Grm1, Metabotropic glutamate receptor 1, mGluR1
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-mGluR1a antibody [EPR24160-173] - BSA and Azide free (AB289639)
Immunohistochemical analysis of 4% PFA-fixed frozen mouse pinnae (fresh) tissue labelling mGluR1a with ab259888 at 1/500 dilution (0.98 μg/ml) followed by 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 ab150081 at 1/1000 dilution (2 μg/mL).
This data was developed using ab259888, the same antibody clone in a different buffer formulation.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-mGluR1a antibody [EPR24160-173] - BSA and Azide free (AB289639)
This data was developed using ab259888, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse kidney labelling mGluR1a with 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 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.
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-mGluR1a antibody [EPR24160-173] - BSA and Azide free (AB289639)
Immunohistochemical analysis of 4% PFA-fixed frozen rat cerebellum (fresh) tissue labelling mGluR1a with ab259888 at 1/500 dilution (0.98 μg/ml) followed by ab150081 at 1/1000 dilution (2 μg/mL). Positive staining on rat cerebellum is observed.
Secondary antibody control : Secondary antibody is ab150081 at 1/1000 dilution (2 μg/mL).
This data was developed using ab259888, the same antibody clone in a different buffer formulation.
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-mGluR1a antibody [EPR24160-173] - BSA and Azide free (AB289639)
Immunohistochemical analysis of 4% PFA-fixed frozen mouse cerebellum (fresh) tissue labelling mGluR1a with ab259888 at 1/500 dilution (0.98 μg/ml) followed by ab150081 at 1/1000 dilution (2 μg/mL). Positive staining on mouse cerebellum is observed.
Secondary antibody control : Secondary antibody is ab150081 at 1/1000 dilution (2 μg/mL).
This data was developed using ab259888, the same antibody clone in a different buffer formulation.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-mGluR1a antibody [EPR24160-173] - BSA and Azide free (AB289639)
This data was developed using ab259888, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat cerebellum labelling mGluR1a with 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 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.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-mGluR1a antibody [EPR24160-173] - BSA and Azide free (AB289639)
This data was developed using ab259888, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse cerebellum labelling mGluR1a with 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 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.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-mGluR1a antibody [EPR24160-173] - BSA and Azide free (AB289639)
This data was developed using ab259888, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat kidney labelling mGluR1a with 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 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.
- IP
Supplier Data
Immunoprecipitation - Anti-mGluR1a antibody [EPR24160-173] - BSA and Azide free (AB289639)
This data was developed using ab259888, the same antibody clone in a different buffer formulation.
mGluR1a was immunoprecipated from rat cerebellum tissue lysate 10 μg with ab259888 at 1/30 dilution. Western blot was performed on the immunoprecipitate using ab259888 at 1/1000 dilution. VeriBlot for IP secondary antibody (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 (ab172730) instead of 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
false
- IP
Supplier Data
Immunoprecipitation - Anti-mGluR1a antibody [EPR24160-173] - BSA and Azide free (AB289639)
This data was developed using ab259888, the same antibody clone in a different buffer formulation.
mGluR1a was immunoprecipated from mouse cerebellum tissue lysate 10 μg with ab259888 at 1/30 dilution. Western blot was performed on the immunoprecipitate using ab259888 at 1/1000 dilution. VeriBlot for IP secondary antibody (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 (ab172730) instead of 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
false
- WB
Supplier Data
Western blot - Anti-mGluR1a antibody [EPR24160-173] - BSA and Azide free (AB289639)
This data was developed using 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
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 132 kDa
Observed band size: 132 kDa,260 kDa
false
Exposure time: 3min
Related conjugates and formulations (3)
-
Anti-mGluR1a antibody [EPR24160-173]
-
565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-mGluR1a antibody [EPR24160-173]
-
603 Alexa Fluor® 568
Alexa Fluor® 568 Anti-mGluR1a antibody [EPR24160-173]
Reactivity data
Product details
ab289639 is the carrier free version of ab259888
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. 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.
Compatibility
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.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
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.
Pathways
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.
Product protocols
- Visit the General protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com