MYO1F Polyclonal Antibody, 100ul PCR Series Defects in this gene are

Defects in this gene are a cause of susceptibility to familial hypertrigliceridemia

predominantly in the basket terminal ring area

Schwann cells

Members of this family may function as nuclear phosphoproteins that modulate transcription in a promoter context-dependent manner

acting on NADPH

MYO1F Polyclonal Antibody, 100ul PCR Series Defects in this gene areMyosins are actin based motor molecules with ATPase activity. Unconventional myosins serve in intracellular movements. Their highly divergent tails are presumed to bind to membranous compartments, which would be moved relative to actin filaments.,Contains 1 IQ domain.,Contains 1 myosin head like domain.,Contains 1 SH3 domain.,