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MID1 Products

Antibodies
Lysates
MID1 Overexpression Lysate
MID1 Overexpression Lysate
NBL1-13103
Species: Hu
Applications: WB
MID1 Overexpression Lysate
MID1 Overexpression Lysate
NBL1-13102
Species: Hu
Applications: WB
MID1 Overexpression Lysate
MID1 Overexpression Lysate
NBP2-09299
Species: Hu
Applications: WB

Description

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.

Bioinformatics

Entrez Human
Uniprot Human
Human
Human
Human
Human
Human
Product By Gene ID 4281
Alternate Names
  • EC 6.3.2.-
  • FLJ57031
  • FLJ58683
  • FLJ76288
  • FXYGBBB1
  • Midin
  • midline 1 (Opitz/BBB syndrome)
  • RNF59MIDIN
  • TRIM18mouse, homolog of

Research Areas for MID1

Find related products by research area and learn more about each of the different research areas below.

Lipid and Metabolism
Zinc Finger

Related MID1 Blog Posts

Check out the latest blog posts on MID1.
Beta Tubulin III and neurogenesis
Beta tubulin III, also known as Tuj-1, is a class III member of the beta tubulin protein family. Beta tubulins are one of two structural components that form our microtubule network. While general tubulins play a role in a wide range of cellular pr...    Read more.
Read more MID1 related blogs.