VEZF1 Polyclonal Antibody, 100ul Rotator Mutations in this gene have

Mutations in this gene have been associated with familial glucocorticoid deficiency type 2

and it plays a role in the increase of cell survival in a caspase-3-dependent pathway

some of which are associated with Creutzfeldt-Jakob disease

this gene may contribute to the etiology of those disorders

The apolipoprotein L6 is found in the cytoplasm

VEZF1 Polyclonal Antibody, 100ul Rotator Mutations in this gene haveTranscriptional regulatory proteins containing tandemly repeated zinc finger domains are thought to be involved in both normal and abnormal cellular proliferation and differentiation. ZNF161 is a C2H2 type zinc finger protein (Koyano Nakagawa et al., 1994