Species: Hu, Mu, Rt
Applications: WB, ELISA, ICC/IF, IHC, IHC-P
Host: Rabbit Polyclonal
Hu, Bovine, Equine, Guinea Pig, Primate, Porcine, RatApplications:
WB, IP (-)Host:
WB, ELISA, S-ELISAHost:
Applications: WB, ELISA, PA
Defects in the Midline-1 (MID1) gene are the cause of Opitz syndrome, an X-linked recessive disorder characterized by developmental defects. MID1 is a microtubule-associated protein (MAP) with E3 ubiquitin ligase activity. MID1 has been shown to target protein phosphatases 2A (PP2Ac) on microtubules for degradation. MID1 association with PP2A has been proposed to regulate microtubule stabilization for cellular processes such as cell division and migration.
Research Areas for MID1
Find related products by research area and learn more about each of the different research areas below.Lipid and MetabolismZinc Finger
Bioinformatics Tool for MID1
Discover related pathways, diseases and genes to MID1. Need help? Read the Bioinformatics Tool Guide
for instructions on using this tool.