MyoD (Acetyl Lys99/K102) Rabbit Polyclonal Antibody, 100ul Pipette Filler Mice lacking this gene show

Mice lacking this gene show a severe impairment in the migration and homing of lymphocytes

Mutations in this gene are associated with mandibulofacial dysostosis with microcephaly

or other inflammatory stimuli

that is found in the basolateral membranes of hepatocytes

as well as in the regulation of water excretion and cardiovascular functions

MyoD (Acetyl Lys99/K102) Rabbit Polyclonal Antibody, 100ul Pipette Filler Mice lacking this gene showThis gene encodes a nuclear protein that belongs to the basic helix loop helix family of transcription factors and the myogenic factors subfamily. It regulates muscle cell differentiation by inducing cell cycle arrest a prerequisite for myogenic initiation. The protein is also involved in muscle regeneration. It activates its own transcription which may stabilize commitment to myogenesis.