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上海信裕生物科技有限公司
SCN4B抗体

SCN4B抗体

商家询价

产品名称： SCN4B抗体

英文名称： SCN4BAntibody

产品编号： XY 55438-1-

产品价格： null

产品产地： 中国/美国

品牌商标： XYbscience

更新时间： 2023-08-17T09:55:27

使用范围： WB,ELISA,IHC-P,IHC-F,IF

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 SCN4B抗体Applications

Tested Applications: ELISA, WB, IHC
Specificity Reaction: Human, Mouse; Other species are not tested.Please decide the specificity by homology
Positive WB detected in Mouse heart tissue, mouse brain tissue
Positive IHC detected in Human skeletal muscle tissue
Recommended dilution WB : 1:200-1:2000
IHC : 1:20-1:200
 SCN4B抗体Application key: WB=Western Blotting ,IHC=Immunohistochemistry, IF=Immunofluorescence
Images
Prev1NextView more validation data
  • 55438-1-AP;mouse heart tissuemouse heart tissue were subjected to SDS PAGE followed by western blot with 55438-1-AP(SCN4B antibody) at dilution of 1:500
  • 55438-1-AP;human skeletal muscle tissueImmunohistochemistry of paraffin-embedded human skeletal muscle tissue slide using 55438-1-AP( SCN4B Antibody) at dilution of 1:50 (under 10x lens)
  • 55438-1-AP;human skeletal muscle tissueImmunohistochemistry of paraffin-embedded human skeletal muscle tissue slide using 55438-1-AP( SCN4B Antibody) at dilution of 1:50 (under 40x lens)
Product Information SCN4B抗体
Source: Rabbit Purify: Antigen affinity purification
IsoType: IgG Storage: PBS with 0.02% sodium azide and 50% glycerol pH 7.3. -20oC, Avoid freeze / thaw cycles.
Immunogen Information
Immunogen: Peptide Full Name: Sodium channel, voltage-gated, type IV, beta
Caculated Molecular
Weight:		 25 kDa Observed Molecular 
Weight:		 28 kDa
GenbankNo NM_174934 GeneID: 6330
Symbol SCN4B Synonyms SCN4B, Sodium channel subunit beta 4
Background

Mammalian sodium channels are heterotrimers, composed of a central, pore-forming alpha subunit and two auxiliary beta subunits (PMID: 11486343). SCN4B (sodium channel subunit beta-4) is one of several sodium channel beta subunits, which modulate channel gating kinetics. SCN4B has an N-terminal signal peptide, a large extracellular domain predicted to form an Ig-like fold, a single transmembrane alpha helix, and a short cytoplasmic C terminus. Defects in SCN4B gene are a cause of long QT syndrome type 10 (LQT10). SCN4B抗体

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