Anti-GABA A Receptor alpha 3/GABRA3 antibody [EPR28364-82] - BSA and Azide free
- BOND RX™ Validated
- Recombinant
- RabMAb
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Rabbit Recombinant Monoclonal GABA A Receptor alpha 3/GABRA3 antibody. Carrier free. Suitable for WB, IHC-P, IHC-Fr, IP and reacts with Transfected cell lysate - Human, Human, Mouse, Rat samples.
View Alternative Names
Gamma-aminobutyric acid receptor subunit alpha-3, GABA(A) receptor subunit alpha-3, GABAAR subunit alpha-3, GABRA3
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GABA A Receptor alpha 3/GABRA3 antibody [EPR28364-82] - BSA and Azide free (AB316970)
This data was developed using ab316969, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human spleen tissue labeling GABA A Receptor alpha 3/GABRA3 with ab316969 at 1/100 (4.88 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : no staining on human spleen (PMID : 26869349). The section was incubated with ab316969 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 was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GABA A Receptor alpha 3/GABRA3 antibody [EPR28364-82] - BSA and Azide free (AB316970)
This data was developed using ab316969, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human liver tissue labeling GABA A Receptor alpha 3/GABRA3 with ab316969 at 1/100 (4.88 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : no staining on human liver (PMID : 26869349). The section was incubated with ab316969 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 was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GABA A Receptor alpha 3/GABRA3 antibody [EPR28364-82] - BSA and Azide free (AB316970)
This data was developed using ab316969, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human cerebrum tissue labeling GABA A Receptor alpha 3/GABRA3 with ab316969 at 1/100 (4.88 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human cerebrum (PMID : 26869349). The section was incubated with ab316969 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 was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IP
Supplier Data
Immunoprecipitation - Anti-GABA A Receptor alpha 3/GABRA3 antibody [EPR28364-82] - BSA and Azide free (AB316970)
This data was developed using ab316969, the same antibody clone in a different buffer formulation.
GABA A Receptor alpha 3/GABRA3 was immunoprecipitated from 0.35 mg SW1353 (human chondrosarcoma fibroblast) whole cell lysate with ab316969 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab316969 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : SW1353 (human chondrosarcoma fibroblast) whole cell lysate
Lane 2 : ab316969 IP in SW1353 (human chondrosarcoma fibroblast) whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab316969 in SW1353 whole cell lysate
The band at approximately 50KDa may be a degradation/cleavage product.
All lanes:
Immunoprecipitation - Anti-GABA A Receptor alpha 3/GABRA3 antibody [EPR28364-82] (<a href='/en-us/products/primary-antibodies/gaba-a-receptor-alpha-3-gabra3-antibody-epr28364-82-ab316969'>ab316969</a>) at 1/30 dilution
All lanes:
SW1353 (human chondrosarcoma fibroblast) whole cell lysate at 10 µg
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
false
Exposure time: 32s
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-GABA A Receptor alpha 3/GABRA3 antibody [EPR28364-82] - BSA and Azide free (AB316970)
This data was developed using ab316969, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat spleen (fresh frozen) tissue labeling GABA A Receptor alpha 3/GABRA3 with ab316969 at 1/100 (4.88 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/mL) dilution (Green).
Negative control : confocal image showing no staining on rat spleen. The nuclear counterstain was DAPI (Blue). The section was incubated with ab316969 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).
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 3/GABRA3 antibody [EPR28364-82] - BSA and Azide free (AB316970)
This data was developed using ab316969, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat cerebrum (fresh frozen) tissue labeling GABA A Receptor alpha 3/GABRA3 with ab316969 at 1/100 (4.88 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/mL) dilution (Green).
Panel A : merged staining of anti-GABRA3 (ab316969, green), anti-NeuN (ab190565, grey) and anti-GFAP (ab201732, magenta) on rat cerebrum.
Panel B : anti-GABRA3 stained on rat cerebrum.
Panel C : anti-NeuN stained in neurons of rat cerebrum.
Panel D : anti-GFAP stained in astrocytes of rat cerebrum.
The section was incubated in two rounds of staining : in the order of ab316969 and ab190565, ab201732 for 1 hr at room temperature. The nuclear counterstain was DAPI (Blue). 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).
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 3/GABRA3 antibody [EPR28364-82] - BSA and Azide free (AB316970)
This data was developed using ab316969, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse spleen tissue labeling GABA A Receptor alpha 3/GABRA3 with ab316969 at 1/1000 (0.488 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : no staining on mouse spleen. The section was incubated with ab316969 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 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 3/GABRA3 antibody [EPR28364-82] - BSA and Azide free (AB316970)
This data was developed using ab316969, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat spleen tissue labeling GABA A Receptor alpha 3/GABRA3 with ab316969 at 1/1000 (0.488 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : no staining on rat spleen. The section was incubated with ab316969 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 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 3/GABRA3 antibody [EPR28364-82] - BSA and Azide free (AB316970)
This data was developed using ab316969, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse spleen (fresh frozen) tissue labeling GABA A Receptor alpha 3/GABRA3 with ab316969 at 1/100 (4.88 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/mL) dilution (Green).
Negative control : confocal image showing no staining on mouse spleen. The nuclear counterstain was DAPI (Blue). The section was incubated with ab316969 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).
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 3/GABRA3 antibody [EPR28364-82] - BSA and Azide free (AB316970)
This data was developed using ab316969, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labeling GABA A Receptor alpha 3/GABRA3 with ab316969 at 1/1000 (0.488 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse cerebrum. The section was incubated with ab316969 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 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 3/GABRA3 antibody [EPR28364-82] - BSA and Azide free (AB316970)
This data was developed using ab316969, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat cerebrum tissue labeling GABA A Receptor alpha 3/GABRA3 with ab316969 at 1/1000 (0.488 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on rat cerebrum. The section was incubated with ab316969 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 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 3/GABRA3 antibody [EPR28364-82] - BSA and Azide free (AB316970)
This data was developed using ab316969, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse cerebrum (fresh frozen) tissue labeling GABA A Receptor alpha 3/GABRA3 with ab316969 at 1/100 (4.88 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/mL) dilution (Green).
Panel A : merged staining of anti-GABRA3 (ab316969, green), anti-NeuN (ab190565, grey) and anti-GFAP (ab201732, magenta) on mouse cerebrum.
Panel B : anti-GABRA3 stained on mouse cerebrum.
Panel C : anti-NeuN stained in neurons of mouse cerebrum.
Panel D : anti-GFAP stained in astrocytes of mouse cerebrum.
The section was incubated in two rounds of staining : in the order of ab316969 and ab190565, ab201732 for 1 hr at room temperature. The nuclear counterstain was DAPI (Blue). 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).
Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 (2 ug/mL) dilution.
- WB
Supplier Data
Western blot - Anti-GABA A Receptor alpha 3/GABRA3 antibody [EPR28364-82] - BSA and Azide free (AB316970)
This data was developed using ab316969, the same antibody clone in a different buffer formulation.
Negative control : liver (PMID : 26869349), spleen (PMID : 26869349).
In lanes 1-9, the lysates were stored at -80°C prior to Western Blotting. The bands beneath the target band (56 kDa) are likey to be degradation products. In lanes 10-11, the lysates were freshly made and used for Western Blotting immediately to minimize protein degradation.
Lanes 1-4 use Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity to human IgG at 1/2000. Lanes 5-11 use Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1/100000.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
Exposure time : Lanes 1-4 : 3 seconds, lanes 5-7 : 15 seconds, lanes 8-9 : 3 seconds, lanes 10-11 : 59 seconds
All lanes:
Western blot - Anti-GABA A Receptor alpha 3/GABRA3 antibody [EPR28364-82] (<a href='/en-us/products/primary-antibodies/gaba-a-receptor-alpha-3-gabra3-antibody-epr28364-82-ab316969'>ab316969</a>) at 1/1000 dilution
Lane 1:
Human hippocampus tissue lysate at 20 µg
Lane 2:
Human hypothalamus tissue lysate at 20 µg
Lane 3:
Human liver tissue lysate at 20 µg
Lane 4:
Human spleen tissue lysate at 20 µg
Lanes 5 and 10:
Mouse brain tissue lysate at 20 µg
Lane 6:
Mouse cerebellum tissue lysate at 20 µg
Lane 7:
Mouse spleen tissue lysate at 20 µg
Lanes 8 and 11:
Rat brain tissue lysate at 20 µg
Lane 9:
Rat spleen tissue lysate at 20 µg
Secondary
Lanes 1 - 4:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Lanes 5 - 11:
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: 56 kDa,36 kDa
false
- WB
Supplier Data
Western blot - Anti-GABA A Receptor alpha 3/GABRA3 antibody [EPR28364-82] - BSA and Azide free (AB316970)
This data was developed using ab316969, the same antibody clone in a different buffer formulation.
Low expression : MCF7 (PMID : 26869349), HepG2.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 28472809).
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-GABA A Receptor alpha 3/GABRA3 antibody [EPR28364-82] (<a href='/en-us/products/primary-antibodies/gaba-a-receptor-alpha-3-gabra3-antibody-epr28364-82-ab316969'>ab316969</a>) at 1/1000 dilution
Lane 1:
SW1353 (human chondrosarcoma fibroblast) whole cell lysate at 20 µg
Lane 2:
MCF7 (human breast adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 3:
HepG2 (human hepatocellar carcinoma epithelial cell) whole cell 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
Observed band size: 56 kDa,36 kDa
false
Exposure time: 48s
- WB
Supplier Data
Western blot - Anti-GABA A Receptor alpha 3/GABRA3 antibody [EPR28364-82] - BSA and Azide free (AB316970)
This data was developed using ab316969, the same antibody clone in a different buffer formulation.
This antibody does not cross-react with human GBRA1, GBRA2, GBRA4, GBRA5, GBRA6.
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-Histone H3 antibody [EPR16987] - Nuclear Marker and ChIP Grade (ab176842) staining at 1/100000 dilution.
In Western blot, Anti-Myc tag antibody staining at 1/1000 dilution.
All lanes:
Western blot - Anti-GABA A Receptor alpha 3/GABRA3 antibody [EPR28364-82] (<a href='/en-us/products/primary-antibodies/gaba-a-receptor-alpha-3-gabra3-antibody-epr28364-82-ab316969'>ab316969</a>) at 1/1000 dilution
Lane 1:
293T (human embryonic kidney epithelial cell) transfected with an empty vector containing a myc-His-tag®, whole cell lysate at 20 µg
Lane 2:
293T transfected with a human GBRA1 expression vector containing a myc-His-tag®, whole cell lysate at 20 µg
Lane 3:
293T transfected with a human GBRA2 expression vector containing a myc-His-tag®, whole cell lysate at 20 µg
Lane 4:
293T transfected with a human GBRA3 expression vector containing a myc-His-tag®, whole cell lysate at 20 µg
Lane 5:
293T transfected with a human GBRA4 expression vector containing a myc-His-tag®, whole cell lysate at 20 µg
Lane 6:
293T transfected with a human GBRA5 expression vector containing a myc-His-tag®, whole cell lysate at 20 µg
Lane 7:
293T transfected with a human GBRA6 expression vector containing a myc-His-tag®, whole cell 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
Observed band size: 56 kDa,15 kDa
false
Exposure time: 180s
Related conjugates and formulations (1)
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Anti-GABA A Receptor alpha 3/GABRA3 antibody [EPR28364-82]
Reactivity data
Product details
ab316970 is the carrier-free version of ab316969.
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