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MYL3 Polyclonal Antibody, 50ul Immune Cell Analysis This enzyme is distinct from

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MYL3 Polyclonal Antibody, 50ul Immune Cell Analysis This enzyme is distinct fromMYL3 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.

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Description

This enzyme is distinct from another mitochondrial matrix enzyme| dimethylglycine dehydrogenase| which catalyzes a reaction resulting in the formation of sarcosine

WNT2 and WNT7B

Mediates the proteolytic cleavage of HP/haptoglobin in the endoplasmic reticulum

which sequesters the GLUT4 in intracellular vesicles in muscle and fat cells in the absence of insulin

The protein encoded by this gene belongs to the glutamine synthetase family

MYL3 Polyclonal Antibody, 50ul Immune Cell Analysis This enzyme is distinct fromMYL3 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.

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