Human Stathmin 2, STMN2 ELISA Kit , 96T Cell Function Analysis hence preventing their processing into

hence preventing their processing into mature miRNA

Mutations in MC2R can result in familial glucocorticoid deficiency

The encoded protein is a single-pass type I membrane protein and contains 8 immunoglobulin-like C2-type domains

Mutations in this gene cause Alexander disease

Mutations in this gene have been associated with the hepatocerebral form of mitochondrial DNA depletion syndrome (MDDS)

Human Stathmin 2, STMN2 ELISA Kit , 96T Cell Function Analysis hence preventing their processing intoRegulator of microtubule stability. When phosphorylated by MAPK8, stabilizes microtubules and consequently controls neurite length in cortical neurons. In the developing brain, negatively regulates the rate of exit from multipolar stage and retards radial migration from the ventricular zone (By similarity).