| Description : |
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. |
| Source : |
HEK293 |
| Species : |
Human |
| Tag : |
Myc/DDK |
| Molecular Mass : |
53.9 kDa |
| AA Sequence : |
MASGRRAPRTGLLELRAGAGSGAGG ERWQRVLLSLAEDVLTVSPADGDPG PEPGAPREQEPAQLNGAAEPGAGPP QLPEALLLQRRRVTVRKADAGGLGI SIKGGRENKMPILISKIFKGLAADQ TEALFVGDAILSVNGEDLSSATHDE AVQVLKKTGKEVVLEVKYMKDVSPY FKNSTGGTSVGWDSPPASPLQRQPS SPGPTPRNFSEAKHMSLKMAYVSKR CTPNDPEPRYLEICSADGQDTLFLR AKDEASARSWATAIQAQVNTLTPRV KDELQALLAATSTAGSQDIKQIGWL TEQLPSGGTAPTLALLTEKELLLYL SLPETREALSRPARTAPLIATRLVH SGPSKGSVPYDAELSFALRTGTRHG VDTHLFSVESPQELAAWTRQLVDGC HRAAEGVQEVSTACTWNGRPCSLSV HIDKGFTLWAAEPGAARAVLLRQPF EKLQMSSDDGASLLFLDFGGAEGEI QLDLHSCPKTIVFIIHSFLSAKVTR LGLLASGPTRTRPLEQKLISEEDLA ANDILDYKDDDDKV |
| Purity : |
> 80% as determined by SDS-PAGE and Coomassie blue staining |
| Stability : |
Stable for 3 months from receipt of products under proper storage and handling conditions. |
| Storage : |
Store at -80 centigrade. Avoid repeated freeze-thaw cycles. |
| Concentration : |
50 μg/mL as determined by BCA |
| Storage Buffer : |
100 mM glycine, 25 mM Tris-HCl, pH 7.3. |
