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Rabbit anti-Human SCN5A Polyclonal Antibody

The antibody against SCN5A was raised in rabbit using the Synthetic peptide of Human SCN5A as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.

ADC-27507A

The antibody against SCN5A was raised in rabbit using the Synthetic peptide of Human SCN5A as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.

$299.00

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Specifications


Cat.No ADC-27507A ClonalityPolyclonal
Host SpeciesRabbitTarget NameSCN5A
FormLiquidSpecies ReactivityHuman, Mouse, Rat
IsotypeIgGStorage Buffer0.05% NaN3, 40% Glycerol., pH7.4 PBS
Purification MethodAntigen affinity purifiedConjugateNon-conjugated
ApplicationELISA, IHCStorageUpon receipt

Immunogen Information


Immunogen DescriptionSynthetic peptide of Human SCN5ATarget SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDQ14524
Background Information
  • Uniprot Id

    Q14524

  • Target Species

    Human

  • Target Name

    SCN5A

  • Target Full Name

    Sodium channel protein type 5 subunit alpha

  • Target Function

    This protein mediates the voltage-dependent sodium ion permeability of excitable membranes. Assuming opened or closed conformations in response to the voltage difference across the membrane, the protein forms a sodium-selective channel through which Na(+) ions may pass in accordance with their electrochemical gradient. It is a tetrodotoxin-resistant Na(+) channel isoform. This channel is responsible for the initial upstroke of the action potential. Channel inactivation is regulated by intracellular calcium levels.

  • Target Involvement

    Progressive familial heart block 1A (PFHB1A); Long QT syndrome 3 (LQT3); Brugada syndrome 1 (BRGDA1); Sick sinus syndrome 1 (SSS1); Familial paroxysmal ventricular fibrillation 1 (VF1); Sudden infant death syndrome (SIDS); Atrial standstill 1 (ATRST1); Cardiomyopathy, dilated 1E (CMD1E); Atrial fibrillation, familial, 10 (ATFB10)

  • Target Subcellular Location

    Cell membrane; Multi-pass membrane protein. Cytoplasm, perinuclear region. Cell membrane, sarcolemma, T-tubule.

  • Target Protein Families

    Sodium channel (TC 1.A.1.10) family, Nav1.5/SCN5A subfamily

  • Target Tissue Specificity

    Found in jejunal circular smooth muscle cells (at protein level). Expressed in human atrial and ventricular cardiac muscle but not in adult skeletal muscle, brain, myometrium, liver, or spleen. Isoform 4 is expressed in brain.

  • Target Synonyms

    Cardiac tetrodotoxin insensitive voltage dependent sodium channel alpha subunit; CDCD2; CMD1E; CMPD2; HB1; HB2; HBBD; HH1; ICCD; IVF; LQT3; PFHB1; Scn5a (gene name); Scn5a; SCN5A_HUMAN; Sodium channel protein cardiac muscle alpha subunit; Sodium channel protein cardiac muscle subunit alpha; Sodium channel protein type 5 subunit alpha; Sodium channel protein type V alpha subunit; Sodium channel protein type V subunit alpha; SSS1; VF1; Voltage gated sodium channel alpha subunit Nav1.5; Voltage-gated sodium channel subunit alpha Nav1.5

  • Target Background

    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 have been associated with long QT syndrome type 3 (LQT3), atrial fibrillation, cardiomyopathy, and Brugada syndrome 1, all autosomal dominant cardiac diseases. Alternative splicing results in several transcript variants encoding different isoforms.

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