Rabbit Recombinant Monoclonal SCN9A antibody. Suitable for IHC-Fr, IHC-P, WB, Dot and reacts with Mouse, Rat, Transfected cell lysate - Mouse samples.
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
IHC-Fr | IHC-P | WB | Dot | ICC/IF | |
---|---|---|---|---|---|
Mouse | Tested | Tested | Tested | Expected | Not recommended |
Rat | Tested | Tested | Tested | Expected | Not recommended |
Transfected cell lysate - Mouse | Not recommended | Not recommended | Not recommended | Tested | Not recommended |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info 1/100 | Notes - |
Species Rat | Dilution info 1/100 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell lysate - Mouse | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info 1/100 | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species Rat | Dilution info 1/100 | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell lysate - Mouse | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info 1/1000 | Notes - |
Species Rat | Dilution info 1/1000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell lysate - Mouse | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell lysate - Mouse | Dilution info 1/1000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat, Transfected cell lysate - Mouse | Dilution info - | Notes - |
Pore-forming subunit of Nav1.7, a voltage-gated sodium (Nav) channel that directly mediates the depolarizing phase of action potentials in excitable membranes. Navs, also called VGSCs (voltage-gated sodium channels) or VDSCs (voltage-dependent sodium channels), operate by switching between closed and open conformations depending on the voltage difference across the membrane. In the open conformation they allow Na(+) ions to selectively pass through the pore, along their electrochemical gradient. The influx of Na(+) ions provokes membrane depolarization, initiating the propagation of electrical signals throughout cells and tissues (By similarity). Nav1.7 plays a crucial role in controlling the excitability and action potential propagation from nociceptor neurons, thereby contributing to the sensory perception of pain (PubMed:15314237).
Kiaa4197, Scn9a, Sodium channel protein type 9 subunit alpha, Peripheral sodium channel 1, Sodium channel protein type IX subunit alpha, Voltage-gated sodium channel subunit alpha Nav1.7, PN1
Rabbit Recombinant Monoclonal SCN9A antibody. Suitable for IHC-Fr, IHC-P, WB, Dot and reacts with Mouse, Rat, Transfected cell lysate - Mouse samples.
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
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:
For more information, read more on recombinant antibodies.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
Nav1.7 Dot Blot staining using rabbit Anti-Nav1.7 antibody
Dot blot analysis of Nav1.7 using ab323849 at 1:1000 (0.493 ug/ml) followed by a Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1:100,000 dilution.
Lane1: 293T cells transfected with a mouse SCN2A expression vector containing a His-tag, whole cell lysate
Lane2: 293T cells transfected with a mouse SCN3A expression vector containing a His-tag, whole cell lysate
Lane3: 293T cells transfected with a mouse SCN1A expression vector containing a His-tag, whole cell lysate
Lane4: 293T cells transfected with a mouse SCN9A expression vector containing a His-tag, whole cell lysate
Exposure time: 180 seconds.
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
This antibody does not cross-react with mouse SCN1A, SCN2A and SCN3A.
In Dot Blot, Anti-6X His tag® antibody [EPR20547] - ChIP Grade (Anti-6X His tag® antibody [EPR20547] - ChIP Grade ab213204) staining at 1/5000 dilution.
All lanes: Dot Blot - Anti-Nav1.7 antibody [EPR26246-318] (ab323849) at 1/1000 dilution
Lane 1: 293T cells transfected with a mouse SCN2A expression vector containing a His-tag, whole cell lysate
Lane 2: 293T cells transfected with a mouse SCN3A expression vector containing a His-tag, whole cell lysate
Lane 3: 293T cells transfected with a mouse SCN1A expression vector containing a His-tag, whole cell lysate
Lane 4: 293T cells transfected with a mouse SCN9A expression vector containing a His-tag, whole cell lysate
All lanes: Dot Blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/100000 dilution
Exposure time: 180s
Nav1.7 Western blot staining using rabbit Anti-Nav1.7 antibody
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
Negative control: skeletal muscle (PMID: 9037087).
Samples are non-boiled as boiling may cause protein aggregation.
In lanes 1-2, to minimize protein degradation, tissues were lysed immediately after harvest and then applied to a gel and transfer membrane for Western blotting as soon as possible.
All lanes: Western blot - Anti-Nav1.7 antibody [EPR26246-318] (ab323849) at 1/1000 dilution
Lane 1: Mouse skeletal muscle tissue lysate(Fresh) at 40 µg
Lane 2: Mouse sciatic nerve tissue lysate(Fresh) at 40 µg
Lane 3: Mouse skeletal muscle tissue lysate(Frozen) at 50 µg
Lane 4: Mouse sciatic nerve tissue lysate(Frozen) at 50 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/20000 dilution
Observed band size: 270 kDa, 124 kDa
Exposure time: 180s
Nav1.7 Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) staining of Mouse skeletal muscle using rabbit Anti-Nav1.7 antibody
Immunohistochemical analysis of paraffin-embedded Mouse skeletal muscle tissue labeling Nav1.7 with ab323849 at 1/100 (4.93 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control: No staining on mouse skeletal muscle (PMID: 9037087).
The section was incubated with ab323849 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
Nav1.7 Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) staining of Rat spinal cord using rabbit Anti-Nav1.7 antibody
Immunohistochemical analysis of paraffin-embedded Rat spinal cord tissue labeling Nav1.7 with ab323849 at 1/100 (4.93 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on rat spinal cord.
The section was incubated with ab323849 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
Nav1.7 Immunohistochemistry (Frozen sections) staining of Rat olfactory bulb (fresh frozen) using rabbit Anti-Nav1.7 antibody
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat olfactory bulb (fresh frozen) tissue labeling Nav1.7 with ab323849 at 1/100 (4.93 ug/ml) dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (AlexaFluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green).
Panel A: merged staining of anti-SCN9A (ab323849, green) and anti-Peripherin (Alexa Fluor® 555 Anti-Peripherin antibody [EPR23445-28] ab311892, magenta) on rat olfactory bulb.
Panel B: anti-SCN9A stained on rat olfactory bulb.
Panel C: anti-Peripherin stained in neurons of rat olfactory bulb.
The section was incubated in two rounds of staining: in the order of ab323849 and Alexa Fluor® 555 Anti-Peripherin antibody [EPR23445-28] ab311892 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 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (AlexaFluor® 488) preadsorbedat 1/1000 2 ug/mL dilution.
Nav1.7 Immunohistochemistry (Frozen sections) staining of Mouse olfactory bulb (fresh frozen) using rabbit Anti-Nav1.7 antibody
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse olfactory bulb (fresh frozen) tissue labeling Nav1.7 with ab323849 at 1/100 (4.93 ug/ml) dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (AlexaFluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green).
Panel A: merged staining of anti-SCN9A (ab323849, green) and anti-Peripherin (Alexa Fluor® 555 Anti-Peripherin antibody [EPR23445-28] ab311892, magenta) on mouse olfactory bulb.
Panel B: anti-SCN9A stained on mouse olfactory bulb.
Panel C: anti-Peripherin stained in neurons of mouse olfactory bulb.
The section was incubated in two rounds of staining: in the order of ab323849 and Alexa Fluor® 555 Anti-Peripherin antibody [EPR23445-28] ab311892 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 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (AlexaFluor® 488) preadsorbedat 1/1000 2 ug/mL dilution.
Nav1.7 Western blot staining using rabbit Anti-Nav1.7 antibody
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
Negative control: skeletal muscle (PMID: 9037087).
Samples are non-boiled as boiling may cause protein aggregation.
To minimize protein degradation, lane1-3 were lysed immediately after harvest and then applied to a gel and transfer membrane for Western blotting as soon as possible.
Exposure time: Lane 1: 136 seconds, Lanes 2-3: 10 seconds, Lane 4: 180 seconds
All lanes: Western blot - Anti-Nav1.7 antibody [EPR26246-318] (ab323849) at 1/1000 dilution
Lane 1: Rat spinal cord tissue lysate(Fresh) at 80 µg
Lane 2: Rat olfactory bulb tissue lysate(Fresh) at 80 µg
Lane 3: Rat skeletal muscle tissue lysate(Frozen) at 80 µg
Lane 4: Rat olfactory bulb tissue lysate(Frozen) at 50 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/20000 dilution
Observed band size: 270 kDa, 124 kDa
Nav1.7 Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) staining of Mouse olfactory bulb using rabbit Anti-Nav1.7 antibody
Immunohistochemical analysis of paraffin-embedded Mouse olfactory bulb tissue labeling Nav1.7 with ab323849 at 1/100 (4.93 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse olfactory bulb.
The section was incubated with ab323849 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
Nav1.7 Immunohistochemistry (Frozen sections) staining of Mouse skeletal muscle (fresh frozen) using rabbit Anti-Nav1.7 antibody
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse skeletal muscle (fresh frozen) tissue labeling Nav1.7 with ab323849 at 1/100 (4.93 ug/ml) dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (AlexaFluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green).
Negative control: confocal image showing no staining on mouse skeletal muscle. The nuclear counterstain was DAPI (Blue). The section was incubated with ab323849 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 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (AlexaFluor® 488) preadsorbedat 1/1000 2 ug/mL dilution.
Nav1.7 Immunohistochemistry (Frozen sections) staining of Rat skeletal muscle (fresh frozen) using rabbit Anti-Nav1.7 antibody
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat skeletal muscle (fresh frozen) tissue labeling Nav1.7 with ab323849 at 1/100 (4.93 ug/ml) dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (AlexaFluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green).
Negative control: confocal image showing no staining on rat skeletal muscle. The nuclear counterstain was DAPI (Blue). The section was incubated with ab323849 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 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (AlexaFluor® 488) preadsorbedat 1/1000 2 ug/mL dilution.
Nav1.7 Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) staining of Rat skeletal muscle using rabbit Anti-Nav1.7 antibody
Immunohistochemical analysis of paraffin-embedded Rat skeletal muscle tissue labeling Nav1.7 with ab323849 at 1/100 (4.93 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control: No staining on rat skeletal muscle.
The section was incubated with ab323849 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
Nav1.7 Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) staining of Rat olfactory bulb using rabbit Anti-Nav1.7 antibody
Immunohistochemical analysis of paraffin-embedded Rat olfactory bulb tissue labeling Nav1.7 with ab323849 at 1/100 (4.93 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on rat olfactory bulb.
The section was incubated with ab323849 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
Nav1.7 Immunohistochemistry (Frozen sections) staining of Rat sciatic nerve (fresh frozen) using rabbit Anti-Nav1.7 antibody
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat sciatic nerve (fresh frozen) tissue labeling Nav1.7 with ab323849 at 1/100 (4.93 ug/ml) dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (AlexaFluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green).
Panel A: merged staining of anti-SCN9A (ab323849, green) and anti-Peripherin (Alexa Fluor® 555 Anti-Peripherin antibody [EPR23445-28] ab311892, magenta) on rat sciatic nerve.
Panel B: anti-SCN9A stained on rat sciatic nerve.
Panel C: anti-Peripherin stained on rat sciatic nerve.
The section was incubated in two rounds of staining: in the order of ab323849 and Alexa Fluor® 555 Anti-Peripherin antibody [EPR23445-28] ab311892 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 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (AlexaFluor® 488) preadsorbedat 1/1000 2 ug/mL dilution.
Nav1.7 Immunohistochemistry (Frozen sections) staining of Mouse sciatic nerve (fresh frozen) using rabbit Anti-Nav1.7 antibody
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse sciatic nerve (fresh frozen) tissue labeling Nav1.7 with ab323849 at 1/100 (4.93 ug/ml) dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (AlexaFluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green).
Panel A: merged staining of anti-SCN9A (ab323849, green) and anti-Peripherin (Alexa Fluor® 555 Anti-Peripherin antibody [EPR23445-28] ab311892, magenta) on mouse sciatic nerve.
Panel B: anti-SCN9A stained on mouse sciatic nerve.
Panel C: anti-Peripherin stained on mouse sciatic nerve.
The section was incubated in two rounds of staining: in the order of ab323849 and Alexa Fluor® 555 Anti-Peripherin antibody [EPR23445-28] ab311892 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 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (AlexaFluor® 488) preadsorbedat 1/1000 2 ug/mL dilution.
Nav1.7 Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) staining of Mouse spinal cord using rabbit Anti-Nav1.7 antibody
Immunohistochemical analysis of paraffin-embedded Mouse spinal cord tissue labeling Nav1.7 with ab323849 at 1/100 (4.93 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse spinal cord.
The section was incubated with ab323849 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
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