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

TAL1 and TCF3

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

The protein encoded by this gene shares the synapsin family domain model

RPLP2 (ribosomal protein lateral stalk subunit P2) encodes a ribosomal phosphoprotein that is a component of the 60S subunit

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.