Syntrophin alpha 1 Rabbit pAb
Cat No.: APA3234
Size:
Product Name: | Syntrophin alpha 1 Rabbit pAb |
Cat No.: | APA3234 |
source: | Rabbit |
reactivity: | Human, Mouse |
applications: | WB,IHC,ICC/IF,FC |
clonality: | Polyclonal |
recommended dilution: | WB: 1:1000-1:5000 IHC: 1:50 ICC/IF: 1:50 FC: 1:50 |
format: | Liquid |
isotype: | IgG |
immunogen: | A synthetic peptide of human Syntrophin alpha 1 |
calculated molecular weight: | 54 kDa |
observed molecular weight: | 54 kDa |
genbank accession number: | Q13424 |
gene id (ncbi): | 6640 |
purification method: | Affinity Purification |
conjugate: | Un-conjugated |
storage: | Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide and 0.05% BSA. Stable for 12 months from date of receipt. |
synonyms: | SNT1; LQT12; TACIP1; dJ1187J4.5 |
category: | Primary Ab |
concentration: | 0.5mg/ml |
background: | 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. [provided by RefSeq, Jan 2013] |