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Antibody detects endogenous levels of total MYL3.
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Cardiac myosin light chain 1; CMLC1; MLC-lV/sb; MLC1SB; MLClV; Myosin alkali light chain 1, ventricular; Myosin alkali light chain 1, ventricular/slow skeletal muscle isoform; Myosin light chain 1, slow-twitch muscle B/ventricular isoform; Myosin light chain 3; Myosin light chain 3, alkali, cardiac ventricles; myosin light chain, alkali, cardiac ventricles; myosin, light chain 3, alkali; ventricular, skeletal, slow; myosin, light polypeptide 3; myosin, light polypeptide 3, alkali; ventricular, skeletal, slow; rVMLC1; slow skeletal; ventricular; Ventricular myosin alkali light chain; Ventricular myosin light chain 1; ventricular, skeletal, slow; Ventricular/slow twitch myosin alkali light chain; VLCl
Gene Aliases: CMH8; MLC-lV/sb; MLC1s; MLC1SB; MLC1V; MYL3; Mylc; Mylc1v; VLC1; VLCl
UniProt ID: (Human) P08590, (Mouse) P09542, (Rat) P16409
Entrez Gene ID: (Human) 4634, (Mouse) 17897, (Rat) 24585
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