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Syntrophin alpha 1 Recombinant Rabbit mAb

Cat No.: RMA01783
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  • Western blot analysis of Anti-Syntrophin alpha 1 antibody(RMA01783) Gel: 10%SDS-PAGE Lysate: 20 μg Primary antibody: RMA01783(Syntrophin alpha 1 antibody)at dilution 1:1000 Secondary antibody: Goat anti rabbit IgG (SPA10002)at 1:1000 dilution

Product Name: Syntrophin alpha 1 Recombinant Rabbit mAb
Cat No.: RMA01783
Clonality: Monoclonal
Species Reactivity: Human, Mouse
Tested Applications: WB,IHC,ICC/IF,FC
Recommended Dilution: WB,IHC,ICC/IF,FC
Size: 30ul 50ul 100uL
Format: Liquid
Source: Rabbit
Purification Method: Affinity Purification
Isotype: IgG
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 a
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
Synonyms: SNT1; LQT12; TACIP1; dJ1187J4.5
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]
Category: Primary Ab
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