BMAL2 Rabbit Polyclonal Antibody, 50ul Recombinant Protein Mutations in this gene have

Mutations in this gene have been associated with primary autosomal recessive microcephaly 1 and premature chromosome condensation syndrome

usually in the second year

Recent studies have shown that a C-terminally extended isoform is produced by use of an alternative in-frame translation termination codon via a stop codon readthrough mechanism

growth inhibition or cell differentiation

The expression of this gene can be regulated by insulin

BMAL2 Rabbit Polyclonal Antibody, 50ul Recombinant Protein Mutations in this gene haveThis gene encodes a basic helix loop helix transcription factor belonging to the PAS (PER, ARNT, SIM) superfamily. The PAS proteins play important roles in adaptation to low atmospheric and cellular oxygen levels, exposure to certain environmental pollutants, and diurnal oscillations in light and temperature. This protein forms a transcriptionally active heterodimer with the circadian CLOCK protein, the structurally related MOP4, and hypoxia inducible