Scn3b monoclonal antibody, clone S396-29 (FITC)
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More Files
- More Functions
Western Blot (Tissue lysate)
Western Blot analysis of mouse brain with Scn3b monoclonal antibody, clone S396-29 (FITC) (Cat # MAB17356).
Immunocytochemistry
Immunocytochemical staining of SK-N-BE with Scn3b monoclonal antibody, clone S396-29 (FITC) (Cat # MAB17356). (A) DAPI (blue) nuclear stain. (B) Phalloidin Texas Red F-Actin stain. (C) Scn3b Antibody. (D) Composite.
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Specification
Product Description
Mouse monoclonal antibody raised against full length recombinant rat Scn3b.
Immunogen
Recombinant protein corresponding to full length rat Scn3b.
Host
Mouse
Reactivity
Mouse, Rat
Form
Liquid
Conjugation
FITC
Purification
Protein G purification
Isotype
IgG2b
Recommend Usage
Immunocytochemistry (1:100)
Immunofluorescence (1:100)
Western Blot (1:1000)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS, pH 7.4 (50% glycerol, 0.09% sodium azide).
Storage Instruction
Store at -20°C.
Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot (Tissue lysate)
Western Blot analysis of mouse brain with Scn3b monoclonal antibody, clone S396-29 (FITC) (Cat # MAB17356).Immunocytochemistry
Immunocytochemical staining of SK-N-BE with Scn3b monoclonal antibody, clone S396-29 (FITC) (Cat # MAB17356). (A) DAPI (blue) nuclear stain. (B) Phalloidin Texas Red F-Actin stain. (C) Scn3b Antibody. (D) Composite.Immunofluorescence
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Gene Info — Scn3b
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Publication Reference
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Novel SCN3B mutation associated with brugada syndrome affects intracellular trafficking and function of Nav1.5.
Ishikawa T, Takahashi N, Ohno S, Sakurada H, Nakamura K, On YK, Park JE, Makiyama T, Horie M, Arimura T, Makita N, Kimura A.
Circulation Journal 2013 Apr; 77(4):959.
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Differential modulation of sodium channel gating and persistent sodium currents by the beta1, beta2, and beta3 subunits.
Y Qu, R Curtis, D Lawson, K Gilbride, P Ge, P S DiStefano, I Silos-Santiago, W A Catterall, T Scheuer.
Molecular and Cellular Neurosciences 2001 Nov; 18(5):570.
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Novel SCN3B mutation associated with brugada syndrome affects intracellular trafficking and function of Nav1.5.
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