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.

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

Showing Publications 1 - 2 of 2.

Publications using NBP1-26612	Applications	Species
Jongsma MLM, Bakker N, Voortman LM et al. Systems mapping of bidirectional endosomal transport through the crowded cell Current Biology 2024-10-07 [PMID: 39276769]
Bell JL, Malyukova A, Holien JK et al. TRIM16 acts as an E3 ubiquitin ligase and can heterodimerize with other TRIM family members. PLoS One 2012-01-01 [PMID: 22629402]

Array NBP1-26612

• MID1 Antibodies
• MID1 Lysates