Bcl-Xl Polyclonal Antibody, 100ul Pipette Holder Mutations in this gene have

Mutations in this gene have been associated with hemolytic anemia due to hexokinase deficiency

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It plays a role in the development of the eyes

with the breakpoint associated with the genes encoding the mixed-lineage leukemia and septin 2 proteins

Bcl-Xl Polyclonal Antibody, 100ul Pipette Holder Mutations in this gene haveThe protein encoded by this gene belongs to the BCL 2 protein family. BCL 2 family members form hetero or homodimers and act as anti or pro apoptotic regulators that are involved in a wide variety of cellular activities. The proteins encoded by this gene are located at the outer mitochondrial membrane, and have been shown to regulate outer mitochondrial membrane channel (VDAC) opening. VDAC regulates mitochondrial membrane potential, and thus controls