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Human SCN5A Stable Cell Line-CHO

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Cat.No.
CSC-RI0164
Background
The human SCN5A gene encodes the pore-forming subunit of Nav1.5, a voltage-gated sodium channel expressed in heart and upregulated in breast cancer cells. Mutations in SCN5A are responsible for some forms of long QT and short QT syndromes, progressive cardiac conduction defect, sick sinus node syndrome, and dilated cardiomyopathy, Brugada syndrome, congenital heart block, Nav1.5 channels are anti-targets in cardiac risk assessment.
Growth Properties
Adherent
Morphology
Epithelial-like
Host Cell
CHO-K1
Ship
Dry ice
Gene Information
Official Symbol
SCN5A
Synonyms
SCN5A; sodium channel, voltage-gated, type V, alpha subunit; CMD1E, sodium channel, voltage gated, type V, alpha (long QT syndrome 3); sodium channel protein type 5 subunit alpha; CDCD2; CMPD2; HB1; HB2; HBBD; HH1; ICCD; IVF; long QT syndrome 3; LQT3; Nav1.5; PFHB1; SSS1; voltage-gated sodium channel subunit alpha Nav1.5; sodium channel protein cardiac muscle subunit alpha; cardiac tetrodotoxin-insensitive voltage-dependent sodium channel alpha subunit; VF1; CMD1E;
Gene ID
MIM
UniProt ID
Q14524
Chromosome Location
3p21
Pathway
Axon guidance, organism-specific biosystem; Developmental Biology, organism-specific biosystem; Interaction between L1 and Ankyrins, organism-specific biosystem; L1CAM interactions, organism-specific biosystem; SIDS Susceptibility Pathways, organism-specific biosystem;
Function
calmodulin binding; ion channel activity; protein binding; voltage-gated ion channel activity; voltage-gated sodium channel activity;

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