Anti-GRIK1+GRIK2 antibody [EPR23995-85] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal GluK1 antibody. Carrier free. Suitable for ICC/IF, WB, IHC-P and reacts with Mouse, Human, Rat samples.
View Alternative Names
GLUR5, GRIK1, GluK1, Excitatory amino acid receptor 3, Glutamate receptor 5, EAA3, GluR-5, GluR5
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GRIK1+GRIK2 antibody [EPR23995-85] - BSA and Azide free (AB282286)
This data was developed using ab259886, the same antibody clone in a different buffer formulation.
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] - BSA and Azide free (AB282286)
This data was developed using ab259886, the same antibody clone in a different buffer formulation.
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.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GRIK1+GRIK2 antibody [EPR23995-85] - BSA and Azide free (AB282286)
This data was developed using ab259886, the same antibody clone in a different buffer formulation.
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] - BSA and Azide free (AB282286)
This data was developed using ab259886, the same antibody clone in a different buffer formulation.
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] - BSA and Azide free (AB282286)
This data was developed using ab259886, the same antibody clone in a different buffer formulation.
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 solution2) for 20 minutes.
- WB
Lab
Western blot - Anti-GRIK1+GRIK2 antibody [EPR23995-85] - BSA and Azide free (AB282286)
This data was developed using ab259886, the same antibody clone in a different buffer formulation.
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] (<a href='/en-us/products/primary-antibodies/grik1grik2-antibody-epr23995-85-ab259886'>ab259886</a>) 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] - BSA and Azide free (AB282286)
This data was developed using ab259886, the same antibody clone in a different buffer formulation.
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
Lane 2 : 10 seconds
Lane3 : 26 seconds
All lanes:
Western blot - Anti-GRIK1+GRIK2 antibody [EPR23995-85] (<a href='/en-us/products/primary-antibodies/grik1grik2-antibody-epr23995-85-ab259886'>ab259886</a>) 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] - BSA and Azide free (AB282286)
This data was developed using ab259886, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST
Exposure time : 5.5 seconds
All lanes:
Western blot - Anti-GRIK1+GRIK2 antibody [EPR23995-85] (<a href='/en-us/products/primary-antibodies/grik1grik2-antibody-epr23995-85-ab259886'>ab259886</a>) 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]
Reactivity data
Product details
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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.
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