SCN5A (Human) Recombinant Protein (P01)
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More Files
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Specifications
Product Description
Human SCN5A full-length ORF ( AAH51374.1, 1 a.a. - 223 a.a.) recombinant protein with GST-tag at N-terminal.
Sequence
MANFLLPRGTSSFRRFTRESLAAIEKRMAEKQARGSTTLQESREGLPEEEAPRPQLDLQASKKLPDLYGNPPQELIGEPLEDLDPFYSTQKTFIVLNKGKTIFRFSATNALYVLSPFHPIRRAAVKILVHSLFNMLIMCTILTNCVFMAQHDPPPWTKYVEYTFTAIYTFESLVKILARGFCLHAFTFLRDPWNWLDFSVIIMAASVLGTLFFPMSIQATSTS
Host
Wheat Germ (in vitro)
Theoretical MW (kDa)
51.8
Interspecies Antigen Sequence
Mouse (97)
Preparation Method
Purification
Glutathione Sepharose 4 Fast Flow
Quality Control Testing
12.5% SDS-PAGE Stained with Coomassie Blue.
Storage Buffer
50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
Storage Instruction
Store at -80°C. Aliquot to avoid repeated freezing and thawing.
Note
Best use within three months from the date of receipt of this protein.
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Applications
Enzyme-linked Immunoabsorbent Assay
Western Blot (Recombinant protein)
Antibody Production
Protein Array
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Gene Info — SCN5A
Entrez GeneID
6331GeneBank Accession#
BC051374.1Protein Accession#
AAH51374.1Gene Name
SCN5A
Gene Alias
CDCD2, CMD1E, CMPD2, HB1, HB2, HBBD, HH1, ICCD, IVF, LQT3, Nav1.5, PFHB1, SSS1
Gene Description
sodium channel, voltage-gated, type V, alpha subunit
Gene Ontology
HyperlinkGene Summary
The protein encoded by this gene is an integral membrane protein and tetrodotoxin-resistant voltage-gated sodium channel subunit. This protein is found primarily in cardiac muscle and is responsible for the initial upstroke of the action potential in an electrocardiogram. Defects in this gene are a cause of long QT syndrome type 3 (LQT3), an autosomal dominant cardiac disease. Alternative splicing results in several transcript variants encoding different isoforms. [provided by RefSeq
Other Designations
cardiac sodium channel alpha subunit|sodium channel, voltage-gated, type V, alpha (long QT syndrome 3)|voltage-gated sodium channel type V alpha
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Interactomes
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Diseases
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