Anti-GRIK1+GRIK2 antibody [EPR23995-85]
- BOND RX™ Validated
- 20ul selling size
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal GluK1 antibody. Suitable for WB, ICC/IF, IHC-P and reacts with Recombinant fragment - Mouse, Mouse, Rat, Human samples.
View Alternative Names
GLUR5, GRIK1, GluK1, Excitatory amino acid receptor 3, Glutamate receptor 5, EAA3, GluR-5, GluR5, GLUR6, GRIK2, GluK2, Excitatory amino acid receptor 4, Glutamate receptor 6, EAA4, GluR-6, GluR6
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GRIK1+GRIK2 antibody [EPR23995-85] (AB259886)
Immunohistochemical analysis of paraffin-embedded Human cerebrum tissue labelling GRIK1+GRIK2 with ab259886 at 1/1000 (0.557 ug/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on human cerebrum (PMID : 12783878). The section was incubated with ab259886 for 30 minutes 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 minutes.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-GRIK1+GRIK2 antibody [EPR23995-85] (AB259886)
Immunofluorescent analysis of 4% Paraformaldehyde fixed, 0.1% TritonX-100 permeabilized mouse primary neuron cells labeling GRIK1+GRIK2 with ab259886 at 1/50 dilution (11.14 μg/mL), counterstained with Anti-MAP2 mouse monoclonal antibody (ab11267) at 1/500 dilution (4 μg/mL), followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed (ab150081) secondary antibody at 1/1000 dilution (2 μg/mL), counterstained with Goat Anti-Mouse IgG H&L (Alexa Fluor® 594)/ (ab150120) at 1/1000 dilution (2 μg/mL). Confocal image showing cytoplasmic staining in mouse primary neuron.
Confocal scanning Z step was set as 0.3 μm followed by image processing with maximum Z projection.
Negative control 1 : ab259886 at 1/50 dilution (11.14 μg/mL), followed by ab150120 1/1000 (2 μg/mL).
Negative control 2 : ab11267 1/500 (4 μg/mL), followed by ab150081 1/1000 (2 μg/ml).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GRIK1+GRIK2 antibody [EPR23995-85] (AB259886)
Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labelling GRIK1+GRIK2 with ab259886 at 1/1000 (0.557 ug/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on mouse cerebrum.The section was incubated with ab259886 for 30 minutes 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 minutes.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GRIK1+GRIK2 antibody [EPR23995-85] (AB259886)
Immunohistochemical analysis of paraffin-embedded Mouse lung tissue labelling GRIK1+GRIK2 with ab259886 at 1/1000 (0.557 ug/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Negative control : No staining on mouse lung. The section was incubated with ab259886 for 30 minutes 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 minutes.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GRIK1+GRIK2 antibody [EPR23995-85] (AB259886)
Immunohistochemical analysis of paraffin-embedded Rat cerebrum tissue labelling GRIK1+GRIK2 with ab259886 at 1/1000 (0.557 ug/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on rat cerebrum. The section was incubated with ab259886 for 30 minutes 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 minutes.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GRIK1+GRIK2 antibody [EPR23995-85] (AB259886)
Immunohistochemical analysis of paraffin-embedded Mouse cerebellum tissue labelling GRIK1+GRIK2 with ab259886 at 1/1000 (0.557 ug/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on mouse cerebellum (PMID : 11427689). The section was incubated with ab259886 for 30 minutes 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 solution 2) for 20 minutes.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-GRIK1+GRIK2 antibody [EPR23995-85] (AB259886)
Immunofluorescent analysis of 4% Paraformaldehyde fixed, 0.1% TritonX-100 permeabilized rat primary neuron cells labeling GRIK1+GRIK2 with ab259886 at 1/50 dilution (11.14 μg/mL), counterstained with Anti-MAP2 mouse monoclonal antibody (ab11267) at 1/500 dilution (4 μg/mL), followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed (ab150081) secondary antibody at 1/1000 dilution (2 μg/mL), counterstained with Goat Anti-Mouse IgG H&L (Alexa Fluor® 594)/ (ab150120) at 1/1000 dilution (2 μg/mL). Confocal image showing cytoplasmic staining in mouse primary neuron.
Confocal scanning Z step was set as 0.3 μm followed by image processing with maximum Z projection.
Negative control 1 : ab259886 at 1/50 dilution (11.14 μg/mL), followed by ab150120 1/1000 (2 μg/mL).
Negative control 2 : ab11267 1/500 (4 μg/mL), followed by ab150081 1/1000 (2 μg/ml).
- WB
Lab
Western blot - Anti-GRIK1+GRIK2 antibody [EPR23995-85] (AB259886)
Blocking and diluting buffer and concentration : 5% NFDM/TBST
Bands around 250kDa and above might be dimer and tetramer according to the Uniprot database.
Samples are non-boiled as boiling may cause protein aggregates.
Exposure time : Lane1 : 48 seconds
Lane2 : 10 seconds
Lane 3 : 26 seconds
All lanes:
Western blot - Anti-GRIK1+GRIK2 antibody [EPR23995-85] (ab259886) at 1/1000 dilution
Lane 1:
Human hypothalamus tissue lysate at 20 µg
Lane 2:
Human cerebellum tissue lysate at 20 µg
Lane 3:
Rat cerebellum tissue lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 109 kDa
false
- WB
Lab
Western blot - Anti-GRIK1+GRIK2 antibody [EPR23995-85] (AB259886)
Blocking and diluting buffer and concentration : 5% NFDM/TBST
Negative control : Mouse lung (PMID : 15014126)
Samples are non-boiled as boiling may cause protein aggregates.
Exposure time : 26 seconds
All lanes:
Western blot - Anti-GRIK1+GRIK2 antibody [EPR23995-85] (ab259886) at 1/1000 dilution
Lane 1:
Mouse hypothalamus tissue lysate at 20 µg
Lane 2:
Mouse cerebellum tissue lysate at 20 µg
Lane 3:
Mouse lung tissue lysate at 40 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 1/50000 dilution
Observed band size: 109 kDa
false
- WB
Lab
Western blot - Anti-GRIK1+GRIK2 antibody [EPR23995-85] (AB259886)
Blocking and diluting buffer and concentration : 5% NFDM/TBST
Exposure time : 5.5 seconds
All lanes:
Western blot - Anti-GRIK1+GRIK2 antibody [EPR23995-85] (ab259886) at 1/1000 dilution
Lane 1:
Mouse GRIK1 recombinant protein at 0.0005 µg
Lane 2:
Mouse GRIK2 recombinant protein at 0.0005 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
Observed band size: 109 kDa
false
Related conjugates and formulations (1)
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Anti-GRIK1+GRIK2 antibody [EPR23995-85] - BSA and Azide free
Reactivity data
Product details
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.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Kainate receptors which include GRIK1 and GRIK2 form ion channels upon ligand binding allowing the flow of cations such as sodium and calcium across the cell membrane. These interactions significantly influence synaptic strength and neuronal communication. GRIK1 and GRIK2 often assemble in a tetrameric complex which may also include other subunits like GRIK3 enhancing the diversity of receptor functions. The activity of these receptors has a profound impact on neurodevelopment and cognitive processes.
Pathways
GRIK1 and GRIK2 play a pivotal role in glutamatergic signaling pathways specifically impacting synaptic plasticity and long-term potentiation (LTP). These pathways are critical for learning and memory formation. The kainate receptor functions alongside AMPA and NMDA receptors key participants in synaptic transmission. The collaborative interactions among these receptor types facilitate complex neuronal network activities. This involvement positions GRIK1 and GRIK2 as essential players in mediating excitatory neurotransmission that influences higher cognitive functions.
Product protocols
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Target data
Additional targets
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