Human Stathmin 2, STMN2 ELISA Kit , 96T Cell Function Analysis Mutations in this gene have

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

Mutations in this gene cause Alexander disease

This protein may be a negative regulator of apoptosis in photoreceptor cells

2mL/PCR8×4

hence preventing their processing into mature miRNA

Human Stathmin 2, STMN2 ELISA Kit , 96T Cell Function Analysis Mutations in this gene haveRegulator 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).