Anti-ASIC3 antibody [EPR26557-80] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal ASIC3 antibody. Carrier free. Suitable for WB, IHC-P, ICC/IF, IP and reacts with Mouse, Rat, Transfected cell line - Mouse samples.
View Alternative Names
Accn3, Drasic, Asic3, Acid-sensing ion channel 3, ASIC3, Amiloride-sensitive cation channel 3, Dorsal root ASIC, DRASIC
- ICC
Supplier Data
Immunocytochemistry - Anti-ASIC3 antibody [EPR26557-80] - BSA and Azide free (AB302777)
This data was developed using ab302776, the same antibody clone in a different buffer formulation.Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized 293T (human embryonic kidney epithelial cell) cells labelling ASIC3 with ab302776 at 1/4000 (0.124 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green). Confocal image showing positive staining in HEK-293T cells transfected with a mouse ASIC3 expression vector containing a myc tag. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8). ICC has not been tested with endogenous material. is observed. Myc-Tag Mouse mAb (Alexa Fluor® 647) was used to counterstain tubulin at 1/100 0.38 ug/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 2 ug/ml dilution.
- IHC
Supplier Data
Immunohistochemistry - Anti-ASIC3 antibody [EPR26557-80] - BSA and Azide free (AB302777)
This data was developed using ab302776, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Mouse testis tissue labeling ASIC3 with ab302776 at 1/5000 (0.1 ug/ml) followed by a LeicaDS9800 (Bond Polymer Refine Detection) was used at Ready to use dilution. Negative control : no staining on mouse testis (PMID : 11872753). The section was incubated with ab302776 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 LeicaDS9800 (Bond Polymer Refine Detection) was used at Ready to use dilution. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- IHC
Supplier Data
Immunohistochemistry - Anti-ASIC3 antibody [EPR26557-80] - BSA and Azide free (AB302777)
This data was developed using ab302776, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Mouse dorsal root ga tissue labeling ASIC3 with ab302776 at 1/5000 (0.1 ug/ml) followed by a LeicaDS9800 (Bond Polymer Refine Detection) was used at Ready to use dilution. Positive staining on mouse dorsal root ganglion. The section was incubated with ab302776 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 LeicaDS9800 (Bond Polymer Refine Detection) was used at Ready to use dilution. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- IHC
Supplier Data
Immunohistochemistry - Anti-ASIC3 antibody [EPR26557-80] - BSA and Azide free (AB302777)
This data was developed using ab302776, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Rat dorsal root gang tissue labeling ASIC3 with ab302776 at 1/5000 (0.1 ug/ml) followed by a LeicaDS9800 (Bond Polymer Refine Detection) was used at Ready to use dilution. Positive staining on rat dorsal root ganglion (PMID : 9707631). The section was incubated with ab302776 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 LeicaDS9800 (Bond Polymer Refine Detection) was used at Ready to use dilution. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- IP
Supplier Data
Immunoprecipitation - Anti-ASIC3 antibody [EPR26557-80] - BSA and Azide free (AB302777)
This data was developed using ab302776, the same antibody clone in a different buffer formulation.
ASIC3 was immunoprecipitated from 0.35 mg rat dorsal ganglion tissue lysate with ab302776 at 1/30 dilution (2 µg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab302776 at 1/1000 dilution.
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Samples are non-boiled as boiling may cause protein aggregates in lane 1.
This blot was developed using a high sensitivity ECL substrate. The high-sensitivity ECL substrate used allows for the detection of proteins in the mid-femtogram range.
All lanes:
Immunoprecipitation - Anti-ASIC3 antibody [EPR26557-80] (<a href='/en-us/products/primary-antibodies/asic3-antibody-epr26557-80-ab302776'>ab302776</a>) at 1/1000 dilution
Lanes 1 - 2:
Rat dorsal ganglion tissue lysate at 10 µg
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/asic3-antibody-epr26557-80-ab302776'>ab302776</a> in rat dorsal ganglion tissue 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
Predicted band size: 58 kDa
Observed band size: 60 kDa
true
Exposure time: 93s
- WB
Lab
Western blot - Anti-ASIC3 antibody [EPR26557-80] - BSA and Azide free (AB302777)
This data was developed using ab302776, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
It is recommended to optimize experimental conditions by increasing the sample loading amount, using a lower antibody dilution ratio, and employing femtogram-level sensitivity substrates.
Lanes 1 - 4:
Western blot - Anti-ASIC3 antibody [EPR26557-80] (<a href='/en-us/products/primary-antibodies/asic3-antibody-epr26557-80-ab302776'>ab302776</a>) at 1/1000 dilution
Lanes 5 - 8:
Western blot - Anti-ASIC3 antibody [EPR26557-87] (<a href='/en-us/products/primary-antibodies/asic3-antibody-epr26557-87-ab305243'>ab305243</a>) at 1/1000 dilution
Lanes 1 and 5:
Mouse dorsal ganglion tissue lysate at 20 µg
Lanes 2 and 6:
Rat dorsal ganglion tissue lysate at 20 µg
Lanes 3 and 7:
Mouse dorsal ganglion tissue lysate at 40 µg
Lanes 4 and 8:
Rat dorsal ganglion 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 1/20000 dilution
Predicted band size: 58 kDa
Observed band size: 60 kDa
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-ASIC3 antibody [EPR26557-80] - BSA and Azide free (AB302777)
This data was developed using ab302776, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST
The MW is consistent with what has been described in the literature (PMID : 17012229).
Negative control : rat : hippocampus, spinal cord, kidney, testis (PMID : 11872753).
Samples are non-boiled as boiling may cause protein aggregates.
This blot was developed using a high sensitivity ECL substrate in lane 6 and 7. The high-sensitivity ECL substrate used allows for the detection of proteins in the mid-femtogram range.
Exposure time :
Lane 1-5 : 180 seconds
Lane 6 and 7 : 37 seconds.
All lanes:
Western blot - Anti-ASIC3 antibody [EPR26557-80] (<a href='/en-us/products/primary-antibodies/asic3-antibody-epr26557-80-ab302776'>ab302776</a>) at 1/1000 dilution
Lane 1:
Rat dorsal ganglion tissue lysate at 75 µg
Lane 2:
Rat hippocampus tissue lysate at 75 µg
Lane 3:
Rat spinal cord tissue lysate at 75 µg
Lane 4:
Rat kidney tissue lysate at 75 µg
Lane 5:
Rat testis tissue lysate at 75 µg
Lane 6:
Mouse dorsal ganglion tissue lysate at 75 µg
Lane 7:
Mouse hippocampus tissue lysate at 75 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 1/20000 dilution
Predicted band size: 58 kDa
Observed band size: 60 kDa
true
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
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
ASIC3 functions through responding to changes in extracellular pH allowing sodium ions to enter cells when the pH decreases. It does not act solo and usually forms homomeric or heteromeric complexes with other ASIC subunits such as ASIC1 or ASIC2. This combination enhances its sensitivity and response diversity to varying acidic conditions contributing to processes like pain sensing and mechanotransduction. In muscle tissue ASIC3 plays a role in sensing metabolic changes that occur during intensive exercise.
Pathways
ASIC3 integrates into systems related to pain and mechanosensory pathways. It participates prominently in the nociceptive signaling pathway associated with the perception of pain induced by protons. ASIC3 works alongside proteins such as TRPV1 another ion channel known for its role in pain and thermal sensation. Interconnected with these pathways ASIC3 impacts physiological responses like hyperalgesia in acidic environments.
Product protocols
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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