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

a protein known to be involved in the homologous recombination and repair of DNA

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

Fibrillar collagen types I-III are synthesized as precursor molecules known as procollagens

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

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