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SSPN encodes a member of the dystrophin-glycoprotein complex (DGC). Additionally we are shipping Sarcospan (Kras Oncogene-Associated Gene) Proteins (5) and many more products for this protein.
Showing 10 out of 16 products:
Human Polyclonal SSPN Primary Antibody for WB - ABIN1881837
Crosbie, Heighway, Venzke, Lee, Campbell: Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex. in The Journal of biological chemistry 1998
Show all 3 references for 1881837
Cow (Bovine) Polyclonal SSPN Primary Antibody for WB - ABIN2782663
Wohlwend, Strasser, Dickmanns, Ficner: Structural basis for RanGTP independent entry of spliceosomal U snRNPs into the nucleus. in Journal of molecular biology 2008
Our data suggest TWIST1 (show TWIST1 Antibodies) and SSPN to be the functionally relevant androgenetic alopecia genes at the 7p21.1 and 12p12.1 risk loci, respectively.
When human SSPN is expressed at three-fold levels in mdx mice, this increas (show DMD Antibodies)e in adhesion complex abundance improves muscle membrane stability, preventing many of the histopathological changes associa (show DMD Antibodies)ted with Duchenne muscular dystrophy
Analysis of sarcospan as a candidate gene for congenital fibrosis of the extraocular muscles type 1.
Frequent polymorphism of peroxisome proliferator activated receptor gamma gene in colorectal cancer containing wild-type K-ras gene.
Sarcospan plays an important mechanical role in stabilizing the dystrophin (show DMD Antibodies)-glycoprotein complex.
crystal structure of Imp (show IMPA1 Antibodies) beta (127-876) in complex SPN1 (1-65) at 2.8-A resolution reveals that Imp (show IMPA1 Antibodies) beta adopts an open conformation, which is unique for a functional Imp (show IMPA1 Antibodies) beta/cargo complex, and resembles the conformation of the Imp (show IMPA1 Antibodies) beta/RanGTP complex
decreased expression of sarcospan at the Fukuyama congenital muscular dystrophy myofiber surfaces.
Human SSPN in transgegnic mice directly interacts with utrophin (show UTRN Antibodies)-glycoprotein comlpex and functions to stabilize utrophin (show UTRN Antibodies) protein without increasing utrophin (show UTRN Antibodies) transcription.
these results demonstrate that SSPN overexpression is well tolerated in mdx (show DMD Antibodies) mice and improves sarcolemma defects that underlie skeletal muscle and pulmonary dysfunction in Duchenne muscular dystrophy (show DMD Antibodies)
regulates cardiac isoproterenol response and prevents Duchenne muscular dystrophy (show DMD Antibodies)-associated cardiomyopathy
Sarcospan-mediated amelioration of muscular dystrophy in mouse model is dependent on the presence of both utrophin (show UTRN Antibodies) and alpha7beta1 integrin.
SSPN is a necessary component of dystrophin (show DMD Antibodies) and Utr (show UTS2R Antibodies) function and that SSPN modulation of integrin signaling is required for extracellular matrix attachment and muscle force development.
Sarcospan-null mice displayed delayed differentiation after cardiotoxin injury caused by loss of utrophin (show UTRN Antibodies) and Akt (show AKT1 Antibodies) signaling
Sspn is downregulated in brain during hypoxia. Knockdown of Sspn increased cultured cell death under hypoxia.
This gene encodes a member of the dystrophin-glycoprotein complex (DGC). The DGC spans the sarcolemma and is comprised of dystrophin, syntrophin, alpha- and beta-dystroglycans and sarcoglycans. The DGC provides a structural link between the subsarcolemmal cytoskeleton and the extracellular matrix of muscle cells. Two alternatively spliced transcript variants that encode different protein isoforms have been described.
sarcospan (Kras oncogene-associated gene)
, K-ras oncogene-associated protein
, Kras oncogene-associated
, kirsten-ras-associated protein
, kirsten-Ras-associated protein