CLC4E Rabbit Polyclonal Antibody, 50ul Cell Culture & Maintenance disease:A chromosomal aberration involving NUT

disease:A chromosomal aberration involving NUT is found in a rare

GO annotations related to this gene include calcium ion binding and heparin binding

are the common cause of chronic hereditary nonspherocytic hemolytic anemia (CNSHA or HNSHA)

rat and bovine orthologs

excellent resistance to chemical corrosion and to high temperatures and pressure Even thickness of plate bottom and side walls

CLC4E Rabbit Polyclonal Antibody, 50ul Cell Culture & Maintenance disease:A chromosomal aberration involving NUTThis gene encodes a member of the C type lectin C type lectin like domain (CTL CTLD) superfamily. Members of this family share a common protein fold and have diverse functions such as cell adhesion cell cell signalling glycoprotein turnover and roles in inflammation and immune response. The encoded type II transmembrane protein is a downstream target of CCAAT enhancer binding protein (C EBP) beta (CEBPB) and may play a role in inflammation.