Anti-ASIC1 antibody [EPR25411-161]
- BOND RX™ Validated
- 20ul selling size
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal ASIC1 antibody. Suitable for IP, IHC-P, WB and reacts with Mouse, Rat, Transfected cell line - Human samples.
View Alternative Names
Accn2, Asic, Bnac2, Asic1, Acid-sensing ion channel 1, ASIC1, Acid-sensing ion channel, Brain sodium channel 2, BNaC2
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ASIC1 antibody [EPR25411-161] (AB300563)
Immunohistochemical analysis of paraffin-embedded Panel A HEK-293T c tissue labeling ASIC1 with ab300563 at 1/5000 (0.1 ug/ml) followed by a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Positive staining on (A) HEK-293T transfected with a human ASIC1 expression vector, no staining on (B) HEK-293T cells transfected with a human ASIC2a expression vector and (C) HEK-293T transfected with an empty vector. The section was incubated with ab300563 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 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-ASIC1 antibody [EPR25411-161] (AB300563)
Immunohistochemical analysis of paraffin-embedded Rat cardiac muscle tissue labeling ASIC1 with ab300563 at 1/1000 (0.498 ug/ml) followed by a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Negative control : no staining in rat cardiac muscle. The section was incubated with ab300563 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 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-ASIC1 antibody [EPR25411-161] (AB300563)
Immunohistochemical analysis of paraffin-embedded Rat dorsal root gang tissue labeling ASIC1 with ab300563 at 1/1000 (0.498 ug/ml) followed by a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Positive staining in rat dorsal root ganglion neurons. The section was incubated with ab300563 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 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-ASIC1 antibody [EPR25411-161] (AB300563)
Immunohistochemical analysis of paraffin-embedded Mouse cardiac muscle tissue labeling ASIC1 with ab300563 at 1/1000 (0.498 ug/ml) followed by a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Negative control : no staining in mouse cardiac muscle. The section was incubated with ab300563 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 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-ASIC1 antibody [EPR25411-161] (AB300563)
Immunohistochemical analysis of paraffin-embedded Mouse dorsal root ga tissue labeling ASIC1 with ab300563 at 1/1000 (0.498 ug/ml) followed by a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Positive staining in mouse dorsal root ganglion neurons. The section was incubated with ab300563 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 with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- IP
Supplier Data
Immunoprecipitation - Anti-ASIC1 antibody [EPR25411-161] (AB300563)
ASIC1 was immunoprecipitated from 0.35 mg Mouse cerebellum tissue lysate 10 ug with ab300563 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab300563 at 1/1000 dilution.
VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
All lanes:
Immunoprecipitation - Anti-ASIC1 antibody [EPR25411-161] (ab300563) at 1/1000 dilution
Lane 1:
Mouse cerebellum tissue lysate at 10 µg
Lane 2:
ab300563 at 1/30 IP in Mouse cerebellum 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 ab300563 in mouse cerebellum 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
Observed band size: 70 kDa,150 kDa
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-ASIC1 antibody [EPR25411-161] (AB300563)
Blocking and diluting buffer and concentration : 5% NFDM/TBST The observed MW is consistent with what has been described in the literature (PMID : 19218436, PMID : 26252376).
All lanes:
Western blot - Anti-ASIC1 antibody [EPR25411-161] (ab300563) at 1/1000 dilution
Lane 1:
Rat brain tissue lysate
Lane 2:
Rat spinal cord tissue lysate
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
Observed band size: 70 kDa,150 kDa
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-ASIC1 antibody [EPR25411-161] (AB300563)
Blocking and diluting buffer and concentration : 5% NFDM/TBST The observed MW is consistent with what has been described in the literature (PMID : 19218436, PMID : 26252376). Negative controls : heart, kidney (PMID : 9037075).
All lanes:
Western blot - Anti-ASIC1 antibody [EPR25411-161] (ab300563) at 1/1000 dilution
Lane 1:
Mouse cerebellum tissue lysate
Lane 2:
Mouse brain tissue lysate
Lane 3:
Mouse spinal cord tissue lysate
Lane 4:
Mouse heart tissue lysate
Lane 5:
Mouse kidney tissue lysate
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 70 kDa,150 kDa
false
Exposure time: 48s
Related conjugates and formulations (1)
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Anti-ASIC1 antibody [EPR25411-161] (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
This ion channel aids in neuronal response to pH drops serving as a sensor for acidification. The ASIC1 subunit can form homotrimers or heterotrimers with other ASIC subunits which impacts the ion conductance properties. This protein's activity affects synaptic plasticity and is involved in both short-term and long-term modulation of neuronal circuits. Changes in its activity can influence neurotransmission and has implications in neurological functionality.
Pathways
ASIC1 is part of the neurophysiological signaling pathways affecting synaptic transmission. It interacts with other proteins like ASIC2 and ASIC3 being implicated in the modulation of sensory perception and pain. Involvement in pathways like the pain-transducing signaling pathway places ASIC1 in a context where it can regulate nociceptive signals. It participates in ion flux alterations that contribute to neuronal excitability and synaptic strength.
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'.
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