• Target：
• MYL3

• Fields：
• >>Cardiac muscle contraction;>>Adrenergic signaling in cardiomyocytes;>>Apelin signaling pathway;>>Hypertrophic cardiomyopathy;>>Dilated cardiomyopathy

• Gene Name：
• MYL3

• Protein Name：
• Myosin light chain 3

• Human Gene Id：
• 4634

• Human Swiss Prot No：
• P08590

• Mouse Swiss Prot No：
• P09542

• Immunogen：
• The antiserum was produced against synthesized peptide derived from human MYL3. AA range:71-120

• Specificity：
• MYL3 Polyclonal Antibody detects endogenous levels of MYL3 protein.

• Formulation：
• Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

• Source：
• Polyclonal, Rabbit,IgG

• Dilution：
• WB 1:500-2000;IHC 1:50-300; ELISA 2000-20000

• Purification：
• The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

• Concentration：
• 1 mg/ml

• Storage Stability：
• -15°C to -25°C/1 year(Do not lower than -25°C)

• Other Name：
• MYL3;Myosin light chain 3;Cardiac myosin light chain 1;CMLC1;Myosin light chain 1; slow-twitch muscle B/ventricular isoform;MLC1SB;Ventricular/slow twitch myosin alkali light chain

• Observed Band(KD)：
• 22kD

• Background：
• MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy. [provided by RefSeq, Jul 2008],

• Function：
• disease:Defects in MYL3 are the cause of cardiomyopathy familial hypertrophic type 8 (CMH8) [MIM:608751]. Familial hypertrophic cardiomyopathy is a hereditary heart disorder characterized by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea, syncope, collapse, palpitations, and chest pain. They can be readily provoked by exercise. The disorder has inter- and intrafamilial variability ranging from benign to malignant forms with high risk of cardiac failure and sudden cardiac death. CMH8 inheritance can be autosomal dominant or recessive.,disease:Defects in MYL3 are the cause of cardiomyopathy hypertrophic with mid-left ventricular chamber type 1 (MVC1) [MIM:608751]. MVC1 is a very rare variant of familial hypertrophic cardiomyopathy, characterized by mid-left ventricular chamber thickening.,function:Regulatory

• Subcellular Location：
• cytosol,muscle myosin complex,myosin complex,sarcomere,A band,I band,

• Expression：
• Heart,Skeletal muscle,

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