AffiAB® Anti-Syntrophin alpha 1 Antibody
Syntrophins are cytoplasmic peripheral membrane scaffold proteins that are components of the dystrophin-associated protein complex. This gene is a member of the syntrophin gene family and encodes the most common syntrophin isoform found in cardiac tissues. The N-terminal PDZ domain of this syntrophin protein interacts with the C-terminus of the pore-forming alpha subunit (SCN5A) of the cardiac sodium channel Nav1.5. This protein also associates cardiac sodium channels with the nitric oxide synthase-PMCA4b (plasma membrane Ca-ATPase subtype 4b) complex in cardiomyocytes. This gene is a susceptibility locus for Long-QT syndrome (LQT) - an inherited disorder associated with sudden cardiac death from arrhythmia - and sudden infant death syndrome (SIDS) . This protein also associates with dystrophin and dystrophin-related proteins at the neuromuscular junction and alters intracellular calcium ion levels in muscle tissue.
Antibody type
Rabbit polyclonal Antibody
Uniprot ID
SwissProt: Q13424 Human; SwissProt: Q61234 Mouse
Recombinant
NO
Conjugation
Non-conjugated
Host
Rabbit
Isotype
IgG
Clone
N/A
KO/KD
N/A
Species reactivity
Human, Mouse, Rat
Tested applications
WB, IF-Cell, FC
Predicted species reactivity
N/A
Immunogen
Synthetic peptide within mouse Syntrophin alpha 1 aa 174-223 / 503.
Storage
Store at +4°C after thawing. Aliquot store at -20°C. Avoid repeated freeze / thaw cycles.
Form
Liquid
Storage buffer
1*PBS (pH7.4) , 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration
1 mg/mL.
Purity
Immunogen affinity purified.
Signal pathway
N/A
Recommended dilutions
WB:1:500-1:2, 000; IF-Cell:1:50-1:100; FC:1:50-1:100
Molecular Weight
Predicted band size: 54 kDa
Subcellular location
Cell junction, Cell membrane, Cytoplasm, Cytoskeleton, Membrane.
Positive control
Mouse skeletal muscle tissue lysate, rat skeletal muscle tissue lysate, SW620, SiHa.