MYOZ2 rabbit pAb
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MYOZ2 rabbit pAb
Background :
The protein encoded by this gene belongs to a family of sarcomeric proteins that bind to calcineurin, a phosphatase involved in calcium-dependent signal transduction in diverse cell types. These family members tether calcineurin to alpha-actinin at the z-line of the sarcomere of cardiac and skeletal muscle cells, and thus they are important for calcineurin signaling. Mutations in this gene cause cardiomyopathy familial hypertrophic type 16, a hereditary heart disorder. [provided by RefSeq, Aug 2011]Description :
The protein encoded by this gene belongs to a family of sarcomeric proteins that bind to calcineurin, a phosphatase involved in calcium-dependent signal transduction in diverse cell types. These family members tether calcineurin to alpha-actinin at the z-line of the sarcomere of cardiac and skeletal muscle cells, and thus they are important for calcineurin signaling. Mutations in this gene cause cardiomyopathy familial hypertrophic type 16, a hereditary heart disorder. [provided by RefSeq, Aug 2011],Product Name Alternative :
MYOZ2 C4orf5UniProt :
Q9NPC6Swiss Prot :
Q9NPC6Reactivity :
Human; Mouse; RatImmunogen :
The antiserum was produced against synthesized peptide derived from the Internal region of human MYOZ2. AA range:21-70Target :
MYOZ2Clonality :
PolyclonalSource :
RabbitApplications :
WB; ELISA; IHCConcentration :
1 mg/mlDilution :
WB 1:500-2000; IHC-p 1:50-300; ELISA 2000-20000Buffer :
-20°C/1 yearMolecular Weight :
30kDStorage Conditions :
-20°C/1 yearObserved Molecular Weight :
30kDFragment :
IgGSubcellular Location :
Cytoplasm, myofibril, sarcomere, Z line . Colocalizes with ACTN1 and PPP3CA at the Z-line of heart and skeletal muscle. .Other Product Names :
MYOZ2 C4orf5Gene ID (Human) :
51778

