NBR1 mouse Monoclonal Antibody(7C3), 20ul Cell Transfection Mutations in CYC1 may cause

Mutations in CYC1 may cause mitochondrial complex III deficiency

This protein plays a role in maintaining cellular structural integrity and also functions in signal transduction and cellular differentiation

It also contains a destruction box (D box) that is required for its degradation by the APC

A pseudogene is described on the X chromosome

The circular arc design at the flask neck and the frosting process treatment enable an easy grip

NBR1 mouse Monoclonal Antibody(7C3), 20ul Cell Transfection Mutations in CYC1 may causeThe protein encoded by this gene was originally identified as an ovarian tumor antigen monitored in ovarian cancer. The encoded protein contains a B box coiled coil motif, which is present in many genes with transformation potential. It functions as a specific autophagy receptor for the selective autophagic degradation of peroxisomes by forming intracellular inclusions with ubiquitylated autophagic substrates. This gene is located on a region of