Anti-GABA A Receptor alpha 2/GABRA2 antibody [EPR26485-185] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
- What is this?
Be the first to review this product! Submit a review
|
(0 Publication)
Rabbit Recombinant Monoclonal GABA A Receptor alpha 2/GABRA2 antibody. Carrier free. Suitable for IP, ICC/IF, IHC-Fr, IHC-P, WB and reacts with Mouse, Rat, Human samples.
View Alternative Names
Gamma-aminobutyric acid receptor subunit alpha-2, GABA(A) receptor subunit alpha-2, GABAAR subunit alpha-2, GABRA2
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-GABA A Receptor alpha 2/GABRA2 antibody [EPR26485-185] - BSA and Azide free (AB307360)
This data was developed using ab307359, the same antibody clone in a different buffer formulation. Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized rat hippocampal neuron cells labelling GABA A Receptor alpha 2/GABRA2 with ab307359 at 1/100 (4.81 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2ug/ml dilution (Green). Confocal image showing cytoplasmic staining in rat hippocampal neuron. Confocal scanning Z step was set as 0.3 ¦Мm followed by image processing with maximum Z projection. Image was taken with a confocal microscope(Leica-Microsystems, TCS SP8). is observed. ab11267 Anti-MAP2 mouse monoclonal antibody was used to counterstain tubulin at 1/500 4ug/ml dilution (Red). The Nuclear counterstain was DAPI (Blue). Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2ug/ml dilution.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-GABA A Receptor alpha 2/GABRA2 antibody [EPR26485-185] - BSA and Azide free (AB307360)
This data was developed using ab307359, the same antibody clone in a different buffer formulation. Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized mouse primary neuron cells labelling GABA A Receptor alpha 2/GABRA2 with ab307359 at 1/100 (4.81 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2ug/ml dilution (Green). Confocal image showing cytoplasmic staining in mouse primary neuron. Confocal scanning Z step was set as 0.3 ¦Мm followed by image processing with maximum Z projection. Image was taken with a confocal microscope(Leica-Microsystems, TCS SP8). is observed. ab11267 Anti-MAP2 mouse monoclonal antibody was used to counterstain tubulin at 1/500 4ug/ml dilution (Red). The Nuclear counterstain was DAPI (Blue). Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2ug/ml dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GABA A Receptor alpha 2/GABRA2 antibody [EPR26485-185] - BSA and Azide free (AB307360)
This data was developed using ab307359, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Rat hippocampus tissue labeling GABA A Receptor alpha 2/GABRA2 with ab307359 at 1/2000 (0.241 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection) was used. Positive staining on rat hippocampus (PMID : 23337532). The section was incubated with ab307359 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) was used. Heat mediated antigen retrieval was performed 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-GABA A Receptor alpha 2/GABRA2 antibody [EPR26485-185] - BSA and Azide free (AB307360)
This data was developed using ab307359, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Mouse lung tissue lABeling GABA A Receptor alpha 2/GABRA2 with ab307359 at 1/2000 (0.241 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection) was used. Negative control : No staining on mouse lung. The section was incubated with ab307359 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) was used. Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-GABA A Receptor alpha 2/GABRA2 antibody [EPR26485-185] - BSA and Azide free (AB307360)
This data was developed using ab307359, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeABilized frozen Mouse hippocampus (fresh) tissue lABeling GABA A Receptor alpha 2/GABRA2 with ab307359 at 1/100 (4.81 ug/ml) dilution followed by ab150081 Goat Anti-RABbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green). Confocal image showing positive staining on mouse hippocampus. The nuclear counterstain was DAPI (Blue). The section was incubated with ab307359 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND®RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8). is observed. The nuclear counterstain was DAPI (Blue). Secondary antibody control : Secondary antibody is ab150081 Goat Anti-RABbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 2 ug/mL dilution.
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-GABA A Receptor alpha 2/GABRA2 antibody [EPR26485-185] - BSA and Azide free (AB307360)
This data was developed using ab307359, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeABilized frozen Mouse lung (fresh) tissue lABeling GABA A Receptor alpha 2/GABRA2 with ab307359 at 1/100 (4.81 ug/ml) dilution followed by ab150081 Goat Anti-RABbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green). Low expression : confocal image showing no staining on mouse lung (PMID : 29467616). The nuclear counterstain was DAPI (Blue). The section was incubated with ab307359 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8). is observed. The nuclear counterstain was DAPI (Blue). Secondary antibody control : Secondary antibody is ab150081 Goat Anti-RABbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 2 ug/mL dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GABA A Receptor alpha 2/GABRA2 antibody [EPR26485-185] - BSA and Azide free (AB307360)
This data was developed using ab307359, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Mouse hippocampus tissue labeling GABA A Receptor alpha 2/GABRA2 with ab307359 at 1/2000 (0.241 ug/ml) followed by a ready to use LeicaDS9800 (Bond® Polymer Refine Detection) was used. Positive staining on mouse hippocampus (PMID : 23337532). The section was incubated with ab307359 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) was used. Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-GABA A Receptor alpha 2/GABRA2 antibody [EPR26485-185] - BSA and Azide free (AB307360)
This data was developed using ab307359, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeABilized frozen Rat lung (fresh) tissue lABeling GABA A Receptor alpha 2/GABRA2 with ab307359 at 1/100 (4.81 ug/ml) dilution followed by ab150081 Goat Anti-RABbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green). Low expression : confocal image showing no staining on rat lung (PMID : 29467616). The nuclear counterstain was DAPI (Blue). The section was incubated with ab307359 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8). is observed. The nuclear counterstain was DAPI (Blue). Secondary antibody control : Secondary antibody is ab150081 Goat Anti-RABbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 2 ug/mL dilution.
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-GABA A Receptor alpha 2/GABRA2 antibody [EPR26485-185] - BSA and Azide free (AB307360)
This data was developed using ab307359, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeABilized frozen Rat hippocampus (fresh) tissue lABeling GABA A Receptor alpha 2/GABRA2 with ab307359 at 1/100 (4.81 ug/ml) dilution followed by ab150081 Goat Anti-RABbit IgG H&L (Alexa Fluor®, 488) preadsorbed at 1/1000 2 ug/mL dilution (Green). Confocal image showing positive staining on rat hippocampus. The nuclear counterstain was DAPI (Blue). The section was incubated with ab307359 for 60 mins at room temperature. The section was then mounted using Fluoromount®,.The immunostaining was performed on a Leica Biosystems BOND®, RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8). is observed. The nuclear counterstain was DAPI (Blue). Secondary antibody control : Secondary antibody is ab150081 Goat Anti-RABbit IgG H&L (Alexa Fluor®, 488) preadsorbedat 1/1000 2 ug/mL dilution.
- IP
Supplier Data
Immunoprecipitation - Anti-GABA A Receptor alpha 2/GABRA2 antibody [EPR26485-185] - BSA and Azide free (AB307360)
This data was developed using ab307359, the same antibody clone in a different buffer formulation. GABA A Receptor alpha 2/GABRA2 was immunoprecipitated from 0.35 mg Mouse cerebellum tissue lysate 10 ug with ab307359 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab307359 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution. Lane 1 : Mouse cerebellum tissue lysate 10 ug Lane 2 : ab307359 IP in Mouse cerebellum tissue lysate Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab307359 in mouse cerebellum tissue lysate Blocking and dilution buffer and concentration : 5% NFDM/TBST. Exposure time : 24 seconds
All lanes:
Immunoprecipitation - Anti-GABA A Receptor alpha 2/GABRA2 antibody [EPR26485-185] (<a href='/en-us/products/primary-antibodies/gaba-a-receptor-alpha-2-gabra2-antibody-epr26485-185-ab307359'>ab307359</a>) at 1/1000 dilution
Lane 1:
Mouse cerebellum tissue lysate 10 μg
Lane 2:
Mouse cerebellum tissue lysate
Lane 3:
Rabbit monoclonal IgG (<a href='/en-us/products/primary-antibodies/rabbit-igg-monoclonal-epr25a-isotype-control-ab172730'>ab172730</a>) instead of <a href='/en-us/products/primary-antibodies/gaba-a-receptor-alpha-2-gabra2-antibody-epr26485-185-ab307359'>ab307359</a> in mouse cerebellum tissue lysate
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
Observed band size: 51 kDa
false
Exposure time: 24s
- WB
Supplier Data
Western blot - Anti-GABA A Receptor alpha 2/GABRA2 antibody [EPR26485-185] - BSA and Azide free (AB307360)
This data was developed using 307359, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : Samples are non-boiled as boiling may cause protein aggregates. 48 seconds Exposure time :
All lanes:
Western blot - Anti-GABA A Receptor alpha 2/GABRA2 antibody [EPR26485-185] (<a href='/en-us/products/primary-antibodies/gaba-a-receptor-alpha-2-gabra2-antibody-epr26485-185-ab307359'>ab307359</a>) at 1/1000 dilution
All lanes:
Human hippocampus tissue lysate 40 μg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 51 kDa
false
Exposure time: 48s
- WB
Supplier Data
Western blot - Anti-GABA A Receptor alpha 2/GABRA2 antibody [EPR26485-185] - BSA and Azide free (AB307360)
This data was developed using 307359, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : Low expression : liver, lung (PMID : 29467616) Samples are non-boiled as boiling may cause protein aggregates. 48 seconds Exposure time :
All lanes:
Western blot - Anti-GABA A Receptor alpha 2/GABRA2 antibody [EPR26485-185] (<a href='/en-us/products/primary-antibodies/gaba-a-receptor-alpha-2-gabra2-antibody-epr26485-185-ab307359'>ab307359</a>) at 1/1000 dilution
Lane 1:
Mouse cerebellum tissue lysate 80 μg
Lane 2:
Mouse brain tissue lysate 80 μg
Lane 3:
Mouse lu tissue lysate 80 μg
Lane 4:
Mouse liver tissue lysate 80 μg
Lane 5:
Rat cerebellum tissue lysate 80 μg
Lane 6:
Rat brain tissue lysate 80 μg
Lane 7:
Rat lu tissue lysate 80 μg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 51 kDa
false
Exposure time: 48s
- WB
Supplier Data
Western blot - Anti-GABA A Receptor alpha 2/GABRA2 antibody [EPR26485-185] - BSA and Azide free (AB307360)
This data was developed using 307359, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : Samples are non-boiled as boiling may cause protein aggregates. 5.5 seconds Exposure time :
All lanes:
Western blot - Anti-GABA A Receptor alpha 2/GABRA2 antibody [EPR26485-185] (<a href='/en-us/products/primary-antibodies/gaba-a-receptor-alpha-2-gabra2-antibody-epr26485-185-ab307359'>ab307359</a>) at 1/1000 dilution
Lane 1:
Mouse hippocampus tissue lysate 20 μg
Lane 2:
Rat hippocampus tissue lysate 20 μg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 51 kDa
false
Exposure time: 5.5s
Related conjugates and formulations (1)
-
Anti-GABA A Receptor alpha 2/GABRA2 antibody [EPR26485-185]
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.
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
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
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