MID1 Antibody

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.
MID1
midline 1
E3 ubiquitin-protein ligase Midline-1
:  BBBG1 FXY GBBB1 MIDIN midline 1 RING finger protein OGS1 Opitz/BBB syndrome OS OSX putative transcription factor XPRF RING finger protein 59 RING finger protein Midline-1 RNF59 TRIM18 tripartite motif protein TRIM18 tripartite motif-containing protein 18 XPRF zinc finger on X and Y, mouse, homolog of ZNFXY More... Less...
Product
Specifications
Ordering Information
Human
WB
Between 617 and 667
$339
$99