SFRP3 Polyclonal Antibody, 20ul Organelle Studies Chromosomal translocation of this gene

Chromosomal translocation of this gene with the RARA (retinoic acid receptor| alpha) gene on chromosome 17 have been detected in patients with acute promyelocytic leukemia

Binds one transferrin or HFE molecule per subunit

infections

In addition to its role in inhibiting 9-cis-retinoic acid-dependent RXR alpha transcription activation of the retinoic acid responsive element

SFRP3 Polyclonal Antibody, 20ul Organelle Studies Chromosomal translocation of this geneThe protein encoded by this gene is a secreted protein that is involved in the regulation of bone development. Defects in this gene are a cause of female specific osteoarthritis (OA) susceptibility.