FA8A Rabbit Polyclonal Antibody, 50ul[BT-AP02609] Electronic Pipette Mutations in this gene are

Mutations in this gene are associated with Leigh syndrome resulting from mitochondrial complex I deficiency

This gene encodes the beta subunit of the karyopherin receptor complex which interacts with nuclear localization signals to target nuclear proteins to the nucleus

Neuronal PAS domain-containing protein 2 encoded by NPAS2 is a member of the basic helix-loop-helix (bHLH)-PAS family of transcription factors

Both SSF1 and ppan are essential for cell growth and proliferation

in a region thought to be associated with susceptibility for psychiatric disorders and epilepsy

FA8A Rabbit Polyclonal Antibody, 50ul[BT-AP02609] Electronic Pipette Mutations in this gene aredisease: Defects in F8 are the cause of hemophilia A (HEMA)