HSP27 Polyclonal Antibody, 100ul[BT-AP04253] Pipette Holder Mutations in this gene have

Mutations in this gene have been associated with optic atrophy type 1

Previously| this gene had an official symbol of SLC23A2

Three splice variants have been identified which encode proteins that differ in the length of their carboxy terminal ends

which together with CD3-gamma

this step is thought to be one of the earliest in the caspase activation cascade

HSP27 Polyclonal Antibody, 100ul[BT-AP04253] Pipette Holder Mutations in this gene haveHeat shock protein family B (small) member 1 encoded by HSPB1 is induced by environmental stress and developmental changes. Heat shock protein family B (small) member 1 is involved in stress resistance and actin organization and translocates from the cytoplasm to the nucleus upon stress induction. Defects in HSPB1 are a cause of Charcot Marie Tooth disease type 2F (CMT2F) and distal hereditary motor neuropathy (dHMN).