Recombinant Anti-mGluR1a antibody [EPR24160-173] - BSA and Azide free (ab289639)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR24160-173] to mGluR1a - BSA and Azide free
- Suitable for: IHC-P, WB, IP
- Reacts with: Mouse, Rat
Related conjugates and formulations
Overview
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Product name
Anti-mGluR1a antibody [EPR24160-173] - BSA and Azide free
See all mGluR1a primary antibodies -
Description
Rabbit monoclonal [EPR24160-173] to mGluR1a - BSA and Azide free -
Host species
Rabbit -
Tested applications
Suitable for: IHC-P, WB, IPmore details -
Species reactivity
Reacts with: Mouse, Rat -
Immunogen
Synthetic peptide. This information is proprietary to Abcam and/or its suppliers.
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Positive control
- WB: Mouse brain and cerebellum tissue lysates. Rat brain and cerebellum tissue lysates. IHC-P: Mouse cerebellum and kidney tissue. Rat cerebellum and kidney tissue. IP: Mouse and rat cerebellum tissue lysate.
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General notes
ab289639 is the carrier free version of ab259888
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.
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 production
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C. -
Storage buffer
pH: 7.20
Constituent: 100% PBS -
Carrier free
Yes -
Concentration information loading...
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Purity
Protein A purified -
Clonality
Monoclonal -
Clone number
EPR24160-173 -
Isotype
IgG -
Research areas
Associated products
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Alternative Versions
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Compatible Secondaries
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Isotype control
Applications
The Abpromise guarantee
Our Abpromise guarantee covers the use of ab289639 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Application | Abreviews | Notes |
---|---|---|
IHC-P |
Use at an assay dependent concentration. Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
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WB |
Use at an assay dependent concentration. Predicted molecular weight: 132 kDa.
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IP |
Use at an assay dependent concentration.
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Notes |
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IHC-P
Use at an assay dependent concentration. Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
WB
Use at an assay dependent concentration. Predicted molecular weight: 132 kDa. |
IP
Use at an assay dependent concentration. |
Target
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Function
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. -
Tissue specificity
Detected in brain. -
Involvement in disease
Spinocerebellar ataxia, autosomal recessive, 13 -
Sequence similarities
Belongs to the G-protein coupled receptor 3 family. -
Cellular localization
Cell membrane. - Information by UniProt
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Database links
- Entrez Gene: 14816 Mouse
- Entrez Gene: 24414 Rat
- SwissProt: P97772 Mouse
- SwissProt: P23385 Rat
- Unigene: 391904 Mouse
- Unigene: 482986 Mouse
- Unigene: 87787 Rat
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Alternative names
- Glutamate receptor metabotropic 1 antibody
- GPRC1A antibody
- GRM1 alpha antibody
see all
Images
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All lanes : Anti-mGluR1a antibody [EPR24160-173] (ab259888) at 1/1000 dilution
Lane 1 : Mouse brain tissue lysate
Lane 2 : Mouse cerebellum tissue lysate
Lane 3 : Mouse pinnae tissue lysate
Lane 4 : Rat brain tissue lysate
Lane 5 : Rat cerebellum tissue lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution
Predicted band size: 132 kDa
Observed band size: 132, 260 kDa why is the actual band size different from the predicted?
Exposure time: 3 minutesThis 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. -
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.
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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.
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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.
-
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.
-
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.
-
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.
Protocols
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
Datasheets and documents
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Datasheet download
Certificate of Compliance
References (0)
ab289639 has not yet been referenced specifically in any publications.