HSP27(Phospho S78/82) Polyclonal Antibody, 50ul Sealing Film Mutations in this gene cause

Mutations in this gene cause congenital heart defects| multiple types| 2 (CHTD2)

acting as a homodimer to convert naturally-occuring but harmful superoxide radicals to molecular oxygen and hydrogen peroxide

whereas cyclin B2 is primarily associated with the Golgi region

Depletion of this protein in cancer cells dramatically inhibited cell proliferation and induced apoptosis

HSP27(Phospho S78/82) Polyclonal Antibody, 50ul Sealing Film Mutations in this gene causeThe protein encoded by this gene is induced by environmental stress and developmental changes. The encoded protein is involved in stress resistance and actin organization and translocates from the cytoplasm to the nucleus upon stress induction. Defects in this gene are a cause of Charcot Marie Tooth disease type 2F (CMT2F) and distal hereditary motor neuropathy (dHMN).