MAGE-1 Polyclonal Antibody, 50ul Sampling Tubes An important paralog of this

An important paralog of this gene is HSFX1

Defects in this gene have been associated with Fanconi anemia of complementation group T

and they are activated by binding GTP and inactivated by conversion of GTP to GDP by their intrinsic GTPase activity

The differences between S-COMT and MB-COMT reside within the N-termini

a severe mitochondrial encephalomyopathy

MAGE-1 Polyclonal Antibody, 50ul Sampling Tubes An important paralog of thisMAGEA1 is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary