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The protein encoded by MYOZ1 is primarily expressed in the skeletal muscle, and belongs to the myozenin family. Additionally we are shipping Myozenin 1 Proteins (8) and many more products for this protein.
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Our results implicate MYOZ1 as the causative gene at the chromosome 10q22 locus for AF.
Our findings provide evidence for a novel connection between the Z-disc protein calsarcin-2 and the sarcolemma via filamins and beta1 integrins.
Mutations in PDLIM3 (show PDLIM3 Antibodies) and MYOZ1, encoding myocyte Z line proteins, do not play any significant role in the genetic etiology of idiopathic DCM.
Mutations in MYOZ1 and MYOZ2 (show MYOZ2 Antibodies) are at least very rare events as an underlying disease mechanism for idiopathic or familial DCM
A large number of variations were found in many of the genes (myozenin 1, gamma-filamin, kinectin-1) in patients with limb-girdle muscular dystrophies and controls.
study defined proximal promoter region of calsarcin-1 (CS-1 (show MYOZ2 Antibodies))& calsarcin-2 (CS-2)genes; data suggest NF-kappaB (show NFKB1 Antibodies) is required for transcription of CS-1 (show CAT Antibodies) gene, but not CS-2
Calsarcin-2 skeletal muscle specific protein deficiency increases execrcise capacity in mice through calcineurin (show PPP3CA Antibodies)/NFAT (show NFATC1 Antibodies) activation.
The protein encoded by this gene is primarily expressed in the skeletal muscle, and belongs to the myozenin family. Members of this family function as calcineurin-interacting proteins that help tether calcineurin to the sarcomere of cardiac and skeletal muscle. They play an important role in modulation of calcineurin signaling.
, myozenin 1
, filamin-, actinin- and telethonin-binding protein
, skeletal muscle-specific protein
, calcineurin-interacting protein 2
, calcineurin-interacting protein-2