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Anti-NaV1.8 (SCN10A)-ATTO Fluor-594 Antibody

PN3, SNS, Sodium channel protein type 10 subunit alpha
Cat #: ASC-016-AR
Alternative Name PN3, SNS, Sodium channel protein type 10 subunit alpha
Lyophilized Powder yes
Type: Polyclonal
Host: Rabbit
Reactivity: h, r
Immunogen
  • Peptide (C)EDEVAAKEGNSPGPQ, corresponding to amino acid residues 1943-1956 of rat NaV1.8 (Accession Q63554). Intracellular, C-terminus.
Accession (Uniprot) Number Q63554
Gene ID 29571
Peptide confirmation Confirmed by amino acid analysis and mass spectrometry.
Homology Mouse - 14/15 amino acid residues identical; human - 7/15 amino acid residues identical.
RRID AB_2341068.
Purity Affinity purified on immobilized antigen.
Form Lyophilized powder. Reconstituted antibody contains phosphate buffered saline (PBS), pH 7.4, 1% BSA, 0.05% NaN3.
Isotype Rabbit IgG.
Label ATTO-594. Maximum absorption 601 nm; maximum fluorescence 627 nm. The fluorescence is excited most efficiently in the 580 - 615 nm range. This label is related to the Rhodamine dyes and can be used with filters used to detect Texas Red and Alexa-594.
Storage before reconstitution The antibody ships as a lyophilized powder at room temperature. Upon arrival, it should be stored at -20°C.
Reconstitution 50 µl double distilled water (DDW).
Antibody concentration after reconstitution 1 mg/ml.
Storage after reconstitution The reconstituted solution can be stored at 4°C, protected from the light, for up to 1 week. For longer periods, small aliquots should be stored at -20°C. Avoid multiple freezing and thawing. Centrifuge all antibody preparations before use (10000 × g 5 min).
Standard quality control of each lot Western blot analysis (unlabeled antibody, #ASC-016), and immunohistochemistry (labeled antibody).
Applications: if, ih
May also work in: ic*
Immunohistochemistry
  • Expression of NaV1.8 in rat DRG
    Expression of NaV1.8 in rat DRG
    Immunohistochemical staining of adult rat dorsal root ganglion (DRG) using Anti-NaV1.8 (SCN10A)-ATTO Fluor-594 Antibody (#ASC-016-AR). A. NaV1.8 labeling (red) appears in the cell bodies of the DRG. Note that the nerve fibers are not stained. B. Nuclear staining using DAPI as counter stain. C. Merged image of A and B.
  • Multiplex staining of NaV1.8 and Synaptophysin in rat DRG
    Multiplex staining of NaV1.8 and Synaptophysin in rat DRG
    Immunohistochemical staining of rat DRG frozen section using Anti-NaV1.8 (SCN10A)-ATTO Fluor-594 Antibody (#ASC-016-AR) and Anti-Synaptophysin Antibody (#ANR-013). A. NaV1.8 staining (red). B. Synaptophysin staining (green). C. Merged image demonstrates a partial overlap in the distribution of NaV1.8 and Synaptophysin within the DRGs. DAPI is used as the counterstain (blue).
  • Multiplex staining of TRPV1 and NaV1.8 in rat DRG
    Multiplex staining of TRPV1 and NaV1.8 in rat DRG
    Immunohistochemical staining of rat dorsal root ganglion (DRG) using Anti-Rat TRPV1 (VR1) (extracellular)-ATTO Fluor-488 Antibody (#ACC-029-AG), (green), (1:60) and Anti-NaV1.8 (SCN10A)-ATTO Fluor-594 Antibody (#ASC-016-AR), (red), (1:60). A. TRPV1 staining. B. NaV1.8 staining. C. Merge of A and B demonstrates partial co-localization of TRPV1 and NaV1.8 channels. Nuclei stained using DAPI as the counterstain (blue).
References
  1. Wu, L. et al. (2002) NeuroReport 13, 2547.
  2. Baker, M.D. and Wood, J.N. (2001) Trends Pharmacol. Sci. 22, 27.
  3. Lai, J. et al. (2003) Curr. Opin. Neurobiol. 13, 291.
  4. Fang, X. et al. (2002) J. Neurosci. 22, 7425.
  5. Fjell, J. et al. (2000) NeuroReport 11, 199.
  6. Renganathan, M. et al. (2003) Brain Res. 959, 235.
Scientific background

Voltage-gated Na+ channels (NaV) are essential for the generation of action potentials and for cell excitability1. NaV channels are activated in response to depolarization and selectively allow flow of Na+ ions. To date, nine NaV α subunits have been cloned and named NaV1.1-1.92,3. The NaV channels are classified into two groups according to their sensitivity to tetrodotoxin (TTX): TTX-sensitive and TTX-resistant channels4,5. Their expression is developmentally regulated and tissue specific.

Two TTX-resistant NaV channels are expressed in dorsal root ganglion (DRG) neurons, NaV1.8 and NaV1.9. The NaV1.8 channel (also called SCN10A, SNS and PN3) is mainly expressed in small-diameter DRG neurons4,6. TTX-resistant channels have been suggested to play an important role in nociceptive transmission.

Recently, the involvement of NaV1.8 in multiple sclerosis (MS) was suggested due to up-regulation of both mRNA and protein in Purkinje cells of MS patients and also in animal models6.

Application key:

CBE- Cell-based ELISA, FC- Flow cytometry, ICC- Immunocytochemistry, IE- Indirect ELISA, IF- Immunofluorescence, IFC- Indirect flow cytometry, IHC- Immunohistochemistry, IP- Immunoprecipitation, LCI- Live cell imaging, N- Neutralization, WB- Western blot

Species reactivity key:

H- Human, M- Mouse, R- Rat
Last update: 16/08/2020

Anti-NaV1.8 (SCN10A) Antibody (#ASC-016) is a highly specific antibody directed against an epitope of the rat protein. The antibody can be used in western blot, immunoprecipitation, immunocytochemistry, and immunohistochemistry applications. It has been designed to recognize NaV1.8 from rat, human, and mouse samples.

Anti-NaV1.8 (SCN10A)-ATTO Fluor-594 Antibody (#ASC-016-AR) is directly labeled with an ATTO-594 fluorescent dye. ATTO dyes are characterized by strong absorption (high extinction coefficient), high fluorescence quantum yield, and high photo-stability. The ATTO-594 fluorescent label belongs to the class of Rhodamine dyes and can be used with fluorescent equipment typically optimized to detect Texas Red and Alexa-594. Anti-NaV1.8 (SCN10A)-ATTO Fluor-594 Antibody is specially suited to experiments requiring simultaneous labeling of different markers.

For research purposes only, not for human use

Applications

Specifications

Scientific Background

Citations

Citations
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