Anti-Nav1.5/SCN5A antibody [EPR25136-48] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
- Advanced Validation
- What is this?
Be the first to review this product! Submit a review
|
(0 Publication)
Rabbit Recombinant Monoclonal SCN5A antibody. Carrier free. Suitable for mIHC, WB, IHC-P and reacts with Mouse, Rat samples.
View Alternative Names
Sodium channel protein type 5 subunit alpha, Sodium channel protein cardiac muscle subunit alpha, Sodium channel protein type V subunit alpha, Voltage-gated sodium channel subunit alpha Nav1.5, mH1, Scn5a
- mIHC
Lab
Multiplex immunohistochemistry - Anti-Nav1.5/SCN5A antibody [EPR25136-48] - BSA and Azide free (AB300049)
This data was developed using ab300048 the same antibody clone in a different buffer formulation.
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded Mouse skeletal muscle tissue staining Nav1.5 with ab300048 at a 1/1000 (5.12 µg/ml) dilution, A2BP1 with ab254413 at 1/2000 (0.26 µg/ml) dilution and Dystrophin with ab218198 at 1/5000 ( 0.110 µg/ml) dilution.
Panel A : merged staining of anti-Nav1.5 (green; Opal™520), anti-A2BP1 (gray; Opal™570) and anti-Dystrophin (magenta; Opal™690) on mouse skeletal muscle.
Panel B : anti-Nav1.5 staining cytoplasm in mouse skeletal muscle.
Panel C : anti-A2BP1 staining nucleus in mouse skeletal muscle.
Panel D : anti-Dystrophin staining membrane in mouse skeletal muscle.
Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab300048, ab254413 and ab218198 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope.
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-Nav1.5/SCN5A antibody [EPR25136-48] - BSA and Azide free (AB300049)
This data was developed using ab300048, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat cardiac muscle tissue labelling Nav1.5/SCN5A with ab300048 at 1/100 (4.98 μg/ml) followed by a ready to use LeicaDS9800 (BOND™ Polymer Refine Detection). Positive staining on rat cardiac muscle (PMID : 23542581) (PMID 18178574). The section was incubated with ab300048 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 with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- mIHC
Lab
Multiplex immunohistochemistry - Anti-Nav1.5/SCN5A antibody [EPR25136-48] - BSA and Azide free (AB300049)
This data was developed using ab300048 the same antibody clone in a different buffer formulation.
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded Mouse cardiac muscle tissue staining Nav1.5 with ab300048 at a 1/1000 (5.12 µg/ml), dilution A2BP1 with ab254413 at 1/2000 (0.26 µg/ml) dilution and Dystrophin with ab218198 at 1/5000 ( 0.110 µg/ml) dilution.
Panel A : merged staining of anti-Nav1.5 (green; Opal™520), anti-A2BP1 (gray; Opal™570) and anti-Dystrophin (magenta; Opal™690) on mouse cardiac muscle.
Panel B : anti-Nav1.5 staining cytoplasm in mouse cardiac muscle.
Panel C : anti-A2BP1 staining nucleus in mouse cardiac muscle.
Panel D : anti-Dystrophin staining membrane in mouse cardiac muscle.
Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab300048, ab254413 and ab218198 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope.
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-Nav1.5/SCN5A antibody [EPR25136-48] - BSA and Azide free (AB300049)
This data was developed using ab300048, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse spleen tissue labelling Nav1.5/SCN5A with ab300048 at 1/100 (4.98 μg/ml) followed by a ready to use LeicaDS9800 (BOND™ Polymer Refine Detection). Negative control : no staining on mouse spleen (PMID : 1309946). The section was incubated with ab300048 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 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-Nav1.5/SCN5A antibody [EPR25136-48] - BSA and Azide free (AB300049)
This data was developed using ab300048, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse cardiac muscle tissue labelling Nav1.5/SCN5A with ab300048 at 1/100 (4.98 μg/ml) followed by a ready to use LeicaDS9800 (BOND™ Polymer Refine Detection) was used. Positive staining on mouse cardiac muscle (PMID : 23542581) (PMID 18178574). The section was incubated with ab300048 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-Nav1.5/SCN5A antibody [EPR25136-48] - BSA and Azide free (AB300049)
This data was developed using ab300048, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat liver tissue labelling Nav1.5/SCN5A with ab300048 at 1/100 (4.98 μ/ml) followed by a ready to use LeicaDS9800 (BOND™ Polymer Refine Detection) was used. Negative control : no staining on rat liver (PMID : 22331407). The section was incubated with ab300048 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 with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- WB
Supplier Data
Western blot - Anti-Nav1.5/SCN5A antibody [EPR25136-48] - BSA and Azide free (AB300049)
This data was developed using ab300048, the same antibody clone in a different buffer formulation.
5% NFDM/TBST was used as a blocking and diluting buffer and concentration.
Negative control : liver, spleen(PMID : 1309946)
Samples are non-boiled as boiling may cause protein aggregates.
This blot was developed using a higher sensitivity ECL substrate.
All lanes:
Western blot - Anti-Nav1.5/SCN5A antibody [EPR25136-48] (<a href='/en-us/products/primary-antibodies/nav15-scn5a-antibody-epr25136-48-ab300048'>ab300048</a>) at 1/1000 dilution
Lane 1:
Mouse heart tissue lysate at 20 µg
Lane 2:
Mouse liver tissue lysate at 20 µg
Lane 3:
Mouse spleen tissue 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
Predicted band size: 226 kDa
Observed band size: 250 kDa
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-Nav1.5/SCN5A antibody [EPR25136-48] - BSA and Azide free (AB300049)
This data was developed using ab300048, the same antibody clone in a different buffer formulation.
5% NFDM/TBST was used as a blocking and diluting buffer and concentration.
Negative control : liver (PMID : 1309946).
Samples are non-boiled as boiling may cause protein aggregates.
This blot was developed using a higher sensitivity ECL substrate.
All lanes:
Western blot - Anti-Nav1.5/SCN5A antibody [EPR25136-48] (<a href='/en-us/products/primary-antibodies/nav15-scn5a-antibody-epr25136-48-ab300048'>ab300048</a>) at 1/1000 dilution
Lane 1:
Rat heart tissue lysate at 20 µg
Lane 2:
Rat liver tissue 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
Predicted band size: 226 kDa
Observed band size: 250 kDa
false
Exposure time: 3min
Related conjugates and formulations (1)
-
Anti-Nav1.5/SCN5A antibody [EPR25136-48]
Reactivity data
Product details
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.
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.
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.
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 conditions
Appropriate long-term storage conditions
Aliquoting information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The sodium channel Nav1.5 is integral to the electrical signaling within the heart. It functions within the cardiac cell membrane and forms part of the larger sodium channel complex. Nav1.5 maintains ionic balance and supports normal cardiac rhythm making it essential for the contraction of the heart. Its expression and function can be influenced by interacting proteins and intracellular signaling molecules.
Pathways
Nav1.5 is an important component in the cardiac action potential generation and conduction pathways. It directly influences the cardiac conduction system and is part of the pathway that encompasses the sodium-potassium pump and other ion channels like Nav1.1 and Nav1.8. Through these pathways Nav1.5 regulates cardiac rhythm and myocardial contractility ensuring efficient heart function.
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