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TYB10 Rabbit Polyclonal Antibody, 100ul Protein Post-translational Modification Defects in this gene are

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TYB10 Rabbit Polyclonal Antibody, 100ul Protein Post-translational Modification Defects in this gene are

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Description

Defects in this gene are a cause of autosomal dominant centronuclear myopathy (ADCNM)

A pseudogene located on chromosome 3 has been identified for this gene

The receptor is expressed on immune cells where it binds to MHC class I molecules on antigen-presenting cells and transduces a negative signal that inhibits stimulation of an immune response

Eukaryotes contain two protein translational systems

NBEAL1 is also found at low levels in peripheral blood leukocytes

TYB10 Rabbit Polyclonal Antibody, 100ul Protein Post-translational Modification Defects in this gene are

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