PRD10 Polyclonal Antibody, 100ul Antibodies Defects in this gene are

Defects in this gene are the cause of nonspherocytic hemolytic anemia and a severe enzyme deficiency can be associated with hydrops fetalis

recombination

disease:A chromosomal aberration involving FOXO4 is found in acute leukemias

RAD9A interacts with BCL2L1| FEN1| PRKCD| RAD9B| HUS1| RAD1| ABL1| RPA1| ATAD5 and RPA2

multiple polyadenylation sites have been reported

PRD10 Polyclonal Antibody, 100ul Antibodies Defects in this gene areThe protein encoded by this gene is a transcription factor that contains C2H2 type zinc fingers. It also contains a positive regulatory domain, which has been found in several other zinc finger transcription factors including those involved in B cell differentiation and tumor suppression. Studies of the mouse counterpart suggest that this protein may be involved in the development of the central nerve system (CNS), as well as in the pathogenesis of