ESPB1 Rabbit Polyclonal Antibody, 20ul Protein Post-translational Modification Increases AURKB activity

Increases AURKB activity

at least one of which encodes a preproprotein that is proteolytically processed to generate the mature protease

Defects in SIX1 are a cause of autosomal dominant deafness type 23 (DFNA23) and branchiootic syndrome type 3 (BOS3)

The human FMO gene family is composed of 5 genes and multiple pseudogenes

PRSS1 encodes a trypsinogen

ESPB1 Rabbit Polyclonal Antibody, 20ul Protein Post-translational Modification Increases AURKB activityThe protein encoded by this gene belongs to the sperm coating protein family of epididymal origin. This protein and its canine homolog are the first known examples of proteins with four tandemly arranged fibronectin type 2 (Fn2) domains in the Fn2 module protein family.