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MABN1586

Sigma-Aldrich

Anti-SCN2A Antibody, clone 5H10.2

clone 5H10.2, from mouse

Sinónimos:

Sodium channel protein type 2 subunit alpha, HBSC II, Sodium channel protein brain II subunit alpha, Sodium channel protein type II subunit alpha, Voltage-gated sodium channel subunit alpha Nav1.2

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About This Item

UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41

biological source

mouse

Quality Level

antibody form

purified antibody

antibody product type

primary antibodies

clone

5H10.2, monoclonal

species reactivity

human

technique(s)

western blot: suitable

isotype

IgG2aκ

NCBI accession no.

UniProt accession no.

target post-translational modification

unmodified

Gene Information

human ... SCN2A(6326)

General description

Sodium channel protein type 2 subunit alpha (UniProt Q99250; also known as HBSC II, Sodium channel protein brain II subunit alpha, Sodium channel protein type II subunit alpha, Voltage-gated sodium channel subunit alpha Nav1.2) is encoded by the SCN2A (also known as EIEE11, BFIS3, NAC2, SCN2A1, SCN2A2) gene (Gene ID 6326) in human. Sodium channels are integral plasma membrane proteins that conduct Na+ transport across the plasma membrane. They are classified as either voltage-gated or ligand-gated based on the nature of the triggering mechanism for channel activation. Voltage-gated sodium channels (VGSCs) are also called voltage-sensitive, voltage-dependent, or Nav channels. VGSCs normally consist of an alpha subunit that forms the ion-conducting pore and one to two beta subunits that have several functions including channel gating modulation, although the expression of the alpha subunit alone is sufficient to produce a functional channel. There exist nine known alpha subunits (Nav1.1 through Nav1.5 encoded by SCN1A through SCN5A and Nav1.6 through Nav1.9 encoded by SCN8A through SCN11A) and four beta subunits (Navbeta1 through Navbeta4 encoded by SCN1B through SCN4B). Beta 1 and beta 3 interact with the alpha subunit non-covalently, whereas beta 2 and beta 4 associate with alpha via disulfide bond. Nav1.2 is a multi-pass membrane protein with 24 membrane regions, having both its N- and C-terminal ends at the cytoplasmic side (a.a. 1-124 & 1777-2005).

Specificity

Clone 5H10.2 targets an epitope in the C-terminal cytoplasmic domain.

Immunogen

Epitope: C-terminal cytoplasmic domain.
GST-tagged recombinant human SCN2A C-terminal cytoplasmic domain fragment.

Application

Research Category
Neuroscience
Research Sub Category
Ion Channels & Transporters
This Anti-SCN2A Antibody, clone 5H10.2 is validated for use in Western Blotting for the detection of SCN2A.

Quality

Evaluated by Western Blotting in human cortex tissue lysate.

Western Blotting Analysis: 0.5 µg/mL of this antibody detected SCN2A in 10 µg of human cortex tissue lysate.

Target description

~227-275 kDa observed. 228.0 kDa calculated. The braod banding pattern observed is consistent with the detection of differentially glycosylated and phosphorylated Nav1.2 protein. Uncharacterized band(s) may appear in some lysates.

Physical form

Format: Purified
Protein G purified.
Purified mouse monoclonal IgG2aκ antibody in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

Storage and Stability

Stable for 1 year at 2-8°C from date of receipt.

Other Notes

Concentration: Please refer to lot specific datasheet.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Referencia del producto
Descripción
Precios

Storage Class

12 - Non Combustible Liquids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificados de análisis (COA)

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Visite la Librería de documentos

Protein interaction studies in human induced neurons indicate convergent biology underlying autism spectrum disorders.
Pintacuda, et al.
Cell genomics, 3, 100250-100250 (2023)

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