AP4M1 Rabbit Polyclonal Antibody, 20ul Molecular Weight Markers Defects in this gene are

Defects in this gene are a cause of premature ovarian failure 9 (POF9)

which are involved in maintaining the transcriptional repressive state of genes over successive cell generations

This apolipoprotein L family member may play a role in lipid exchange and transport throughout the body

The import of proteins containing a nuclear localization signal (NLS) requires the NLS import receptor| a heterodimer of importin alpha and beta subunits also known as karyopherins

The encoded protein regulates erythroid gene expression| plays a role in the transcriptional switch of globin gene promoters| and it activates many other cellular and viral gene promoters

AP4M1 Rabbit Polyclonal Antibody, 20ul Molecular Weight Markers Defects in this gene are