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

Mutations in CYC1 may cause mitochondrial complex III deficiency

and an array of carcinoma cell lines

A pseudogene is described on the X chromosome

and the structural diversity in the gene products arises from alternative mRNA splicing

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