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Syntrophin, alpha 1 (Dystrophin-Associated Protein A1, 59kDa, Acidic Component) (SNTA1) ELISA Kits

Dystrophin is a large, rod-like cytoskeletal protein found at the inner surface of muscle fibers. Additionally we are shipping Syntrophin, alpha 1 (Dystrophin-Associated Protein A1, 59kDa, Acidic Component) Antibodies (83) and Syntrophin, alpha 1 (Dystrophin-Associated Protein A1, 59kDa, Acidic Component) Proteins (7) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
SNTA1 20648  
SNTA1 6640 Q13424
SNTA1 362242  
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Top Syntrophin, alpha 1 (Dystrophin-Associated Protein A1, 59kDa, Acidic Component) ELISA Kits at antibodies-online.com

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Human
96 Tests Log in to see 11 to 13 Days
$875.60
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Cow
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$1,029.60
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$999.43
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Human
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More ELISA Kits for Syntrophin, alpha 1 (Dystrophin-Associated Protein A1, 59kDa, Acidic Component) Interaction Partners

Xenopus laevis Syntrophin, alpha 1 (Dystrophin-Associated Protein A1, 59kDa, Acidic Component) (SNTA1) interaction partners

  1. Ordered disorder of the astrocytic dystrophin (show DMD ELISA Kits)-associated protein complex in the norm and pathology.

Mouse (Murine) Syntrophin, alpha 1 (Dystrophin-Associated Protein A1, 59kDa, Acidic Component) (SNTA1) interaction partners

  1. Alpha-syntrophin deficiency markedly reduces astrocyte swelling during severe hypoosmotic stress/brain edema.

  2. Isolated muscle bundles from SNTA1 mutant mice showed reduced force production after hypo-osmotic shock. In addition, the mutant muscle bundles showed delayed recovery of specific gravity after being exposed to hypo-osmotic conditions.

  3. Ordered disorder of the astrocytic dystrophin (show DMD ELISA Kits)-associated protein complex in the norm and pathology.

  4. alpha-Syntrophin, which resides in nuclei of myocytes, functions as the upstream mediator of nuclear nNOS (show NOS1 ELISA Kits) translocation and nNOS (show NOS1 ELISA Kits)-dependent mitochondrial biogenesis.

  5. the removal of the perivascular pool of AQP4 (show AQP4 ELISA Kits) due to alpha-syntrophin deletion reduces edema formation, especially under pathological conditions and during states associated with elevated K+.

  6. Scaffold proteins alpha-syntrophin and dystrophin (show DMD ELISA Kits) exhibit lower densities in retinal microglia compared with brain astrocytes.

  7. The interaction between the conserved COOH-terminal 125-amino acid domain (which is located in the light chains of MAP1A, MAP1B, and MAP1S) and alpha1-syntrophin is direct and occurs through the pleckstrin homology domain 2 (PH2).

  8. Data show that in Dp71 (show DMD ELISA Kits)-null mice, the levels of beta-dystroglycan (beta-DG) and alpha1-syntrophin (alpha1-Syn (show SYP ELISA Kits)) were lower and utrophin (show UTRN ELISA Kits) expression did not change, and the neuronal nitric oxide synthase (nNOS (show NOS1 ELISA Kits)) expression and activity were increased.

  9. We identified alpha1-syntrophin, a component of the dystrophin (show DMD ELISA Kits)-associated protein complex (DAPC), as a myocilin (show MYOC ELISA Kits)-binding candidate.

  10. Migration of myoblasts from alpha-syntrophin knockout mice could not be stimulated by HGF (show HGF ELISA Kits).

Human Syntrophin, alpha 1 (Dystrophin-Associated Protein A1, 59kDa, Acidic Component) (SNTA1) interaction partners

  1. A novel SNTA1 variant is likely causative for drug induced long-QT syndrome by augmenting the late sodium current.

  2. In a nonreferred nationwide Danish cohort of SIDS (show IDS ELISA Kits) cases, up to 5/66 (7.5%) of SIDS (show IDS ELISA Kits) cases can be explained by genetic variants in the sodium channel complex genes.

  3. our results present a possible mechanism of Rac1 activation involving SNTA1 and emphasise its role in ROS (show ROS1 ELISA Kits) generation, cell migration, and acquisition of malignancy.

  4. Ordered disorder of the astrocytic dystrophin (show DMD ELISA Kits)-associated protein complex in the norm and pathology.

  5. alpha-Syntrophin, which resides in nuclei of myocytes, functions as the upstream mediator of nuclear nNOS (show NOS1 ELISA Kits) translocation and nNOS (show NOS1 ELISA Kits)-dependent mitochondrial biogenesis.

  6. Calcium homeostasis mishandling in Duchenne muscular dystrophy (show DMD ELISA Kits) myotubes depends on store operated calcium entry under the influence alpha1-syntrophin regulation as well as TRPV2 (show TRPV2 ELISA Kits)-dependant cation influx.

  7. The combined mutations of A261V-SNTA1 plus R800L-SCN5A (show SCN5A ELISA Kits) increase the INa (show INA ELISA Kits) current late/peak ratio and time constants of current decay.

  8. In contrast to stomach, lung, colon and rectal cancers, SNTA1 protein was found to be downregulated in esophageal cancers and upregulated in breast cancer.

  9. alpha1D-adrenergic receptors are regulated by syntrophins through a PDZ domain (show INADL ELISA Kits)-mediated interaction

  10. These results establish an SNTA1-based nNOS (show NOS1 ELISA Kits) complex attached to SCN5A (show SCN5A ELISA Kits) as a key regulator of sodium current and suggest that SNTA1 be considered a rare long QT syndrome-susceptibility gene.

Syntrophin, alpha 1 (Dystrophin-Associated Protein A1, 59kDa, Acidic Component) (SNTA1) Antigen Profile

Antigen Summary

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.

Gene names and symbols associated with SNTA1

  • syntrophin, alpha 1 (dystrophin-associated protein A1, 59kDa, acidic component) (SNTA1) antibody
  • syntrophin, alpha 1 (dystrophin-associated protein A1, 59kDa, acidic component) (snta1) antibody
  • syntrophin, acidic 1 (Snta1) antibody
  • syntrophin, alpha 1 (SNTA1) antibody
  • syntrophin, alpha 1 (Snta1) antibody
  • AW228934 antibody
  • dJ1187J4.5 antibody
  • LQT12 antibody
  • MGC147484 antibody
  • SNT1 antibody
  • SNTA1 antibody
  • TACIP1 antibody

Protein level used designations for SNTA1

syntrophin, alpha 1 (dystrophin-associated protein A1, 59kDa, acidic component) , 59 kDa dystrophin-associated protein A1 acidic component 1 , alpha-1-syntrophin , alpha1-syntrophin , syntrophin-1 , acidic alpha 1 syntrophin , dystrophin-associated protein A1, 59kDa, acidic component , pro-TGF-alpha cytoplasmic domain-interacting protein 1 , syntrophin, acidic 1 , 59-1 DAP , alpha-syntrophin

GENE ID SPECIES
458181 Pan troglodytes
496157 Xenopus laevis
709824 Macaca mulatta
780141 Xenopus (Silurana) tropicalis
100597246 Nomascus leucogenys
20648 Mus musculus
6640 Homo sapiens
362242 Rattus norvegicus
485837 Canis lupus familiaris
100151843 Sus scrofa
100009179 Oryctolagus cuniculus
527488 Bos taurus
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