Goat Anti-Syntrophin (alpha 1) Antibody

Q13424

WB, E

Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium current. Cheng J, et al. Circ Arrhythm Electrophysiol, 2009 Dec. PMID 20009079.
alpha-1-syntrophin mutation and the long-QT syndrome: a disease of sodium channel disruption. Wu G, et al. Circ Arrhythm Electrophysiol, 2008 Aug. PMID 19684871.
Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex. Ueda K, et al. Proc Natl Acad Sci U S A, 2008 Jul 8. PMID 18591664.
Global, in vivo, and site-specific phosphorylation dynamics in signaling networks. Olsen JV, et al. Cell, 2006 Nov 3. PMID 17081983.
Uncovering quantitative protein interaction networks for mouse PDZ domains using protein microarrays. Stiffler MA, et al. J Am Chem Soc, 2006 May 3. PMID 16637659.

6640

Peptide-affinity purified goat antibody

AF2059a (0.01 µg/ml) staining of Human Muscle lysate (35 µg protein in RIPA buffer) with (B) and without (A) blocking with the immunising peptide. Primary incubation was 1 hour. Detected by chemiluminescence.

NP_003089; 6640; 20648 (mouse);

100ug/200ul