CD10 Rabbit Polyclonal Antibody, 100ul Protein Expression the rare aging disease Hutchinson-Gilford

the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A

Another locus encoding a bipartite transcript designated POMZP3 contains a duplication of the last four exons of ZP3| including the above described variation| and maps closely to this gene

Among its related pathways are Metabolism and Cytosolic iron-sulfur cluster assembly

Alternative splicing in the 5' untranslated region results in multiple transcript variants that encode the same protein

Inactivating variants of this gene result in the recessive Lutheran null phenotype

CD10 Rabbit Polyclonal Antibody, 100ul Protein Expression the rare aging disease Hutchinson-GilfordThis gene encodes a common acute lymphocytic leukemia antigen that is an important cell surface marker in the diagnosis of human acute lymphocytic leukemia (ALL). This protein is present on leukemic cells of pre B phenotype, which represent 85% of cases of ALL. This protein is not restricted to leukemic cells, however, and is found on a variety of normal tissues. It is a glycoprotein that is particularly abundant in kidney, where it is present on the