Bax mouse Monoclonal Antibody(6F11), 50ul Rotator Multiple transcript variants encoding different

Multiple transcript variants encoding different isoforms have been found for UBXN11

Two transcript variants encoding different isoforms have been found for EHHADH

Defects in TRPS1 are a cause of tricho-rhino-phalangeal syndrome (TRPS) types I-III

Initiated by either Dnmt1 or Met-57

including myofibril necrosis in myopathies and in myocardial ischemia

Bax mouse Monoclonal Antibody(6F11), 50ul Rotator Multiple transcript variants encoding differentThe 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