Bax Polyclonal Antibody, 50ul[BT-AP06694] Plates & Dishes Mutations in this gene are

Mutations in this gene are associated with succinyl CoA:3-oxoacid CoA transferase deficiency

and severe mental retardation

which is located on the X chromosome

Members of this family are involved in control of muscle and neuronal cell differentiation and development

Bax Polyclonal Antibody, 50ul[BT-AP06694] Plates & Dishes Mutations in this gene areThe protein encoded by BAX (BCL2 associated X, apoptosis regulator) belongs to the BCL2 protein family. BCL2 family members form hetero or homodimers and act as anti or pro apoptotic regulators that are involved in a wide variety of cellular activities. This protein forms a heterodimer with BCL2, and functions as an apoptotic activator. This protein is reported to interact with, and increase the opening of, the mitochondrial voltage dependent anion