IVD Rabbit Polyclonal Antibody, 20ul Cell Separation and Collection Mutations in this gene are

Mutations in this gene are associated with SDH-defective infantile leukoencephalopathy (mitochondrial complex II deficiency)

It inhibits signal transduction by increasing the GTPase activity of G protein alpha subunits

This gene also participates in several oncogenic rearrangements resulting in anaplastic lymphoma and mixoid chondrosarcoma| and may play a role in the NF-kappaB pathway

DNA repair protein complementing XP-G cells may also function in other cellular processes

The encoded protein may function as a positive regulator in the T-cell receptor signaling pathway

IVD Rabbit Polyclonal Antibody, 20ul Cell Separation and Collection Mutations in this gene are