ArtNr |
E-AB-12860-120 |
Hersteller |
Elabscience
|
Menge |
120uL |
Kategorie |
|
Typ |
Antibody Polyclonal |
Applikationen |
IHC, ELISA |
Specific against |
Human (Homo sapiens), Mouse (Murine, Mus musculus), Rat (Rattus norvegicus) |
Host |
Rabbit |
Isotype |
IgG |
ECLASS 10.1 |
32160702 |
ECLASS 11.0 |
32160702 |
UNSPSC |
12352203 |
Alias |
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, Sodium channel protein cardiac muscle alpha subunit, Sodium channel protein |
Similar products |
SCN5A, Sodium channel protein type 5 subunit alpha, HH1, Sodium channel protein cardiac muscle subunit alpha, Sodium channel protein type V subunit alpha, Voltage-gated sodium channel subunit alpha Nav1.5, HB1, HB2, CDCD2, CMD1E, CMPD2, HBBD, ICCD, IVF, LQT3, PFHB1, SSS1, VF1, Cardiac tetrodotoxin insensitive voltage dependent sodium channel alpha subunit, Scn5a (gene name), Scn5a, Sodium channel protein cardiac muscle alpha subunit, Sodium channel protein type V alpha subunit, Voltage gated sodium channel alpha subunit Nav1.5 |
Lieferbar |
|
Research Areas |
Cancer, Cardiovascular, Neuroscience |
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, 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 |
Swissprot |
Q14524 |
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 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. |
Concentration |
0.3 mg/mL |
Storage |
Store at -20C. Avoid freeze / thaw cycles. |
Immunogen |
Synthetic peptide of human SCN5A |
Buffer |
PBS with 0.05% sodium azide and 50% glycerol, PH7.4 |
Purification Method |
Affinity purification |
Dilution |
IHC 1:25-1:100 |
Conjugation |
Unconjugated |
Gene Accession |
NP_932173 |
Santa Cruz # |
sc-23174, sc-23172, sc-22758 |
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