ANGPTL3 Rabbit Polyclonal Antibody, 20ul Gene Synthesis Mutations in this gene are

Mutations in this gene are a cause of Cushing disease and adrenocortical hyperplasia

chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1

Interleukin-24 encoded by this gene can induce apoptosis selectively in various cancer cells

The coreceptor functions as either a homodimer composed of two alpha chains or as a heterodimer composed of one alpha and one beta chain

F-box proteins interact with SKP1 through the F box

ANGPTL3 Rabbit Polyclonal Antibody, 20ul Gene Synthesis Mutations in this gene areContains 1 fibrinogen C terminal domain. tissue specificity: Expressed principally in liver. Weakly expressed in kidney.