FGF-19 Rabbit Polyclonal Antibody, 50ul[BT-AP10035] Molecular Biologyn MIM 610610)

MIM 610610)

This intronless gene is deleted in AMME contiguous gene syndrome and may be involved in the cardiac and neurologic abnormalities found in the AMME contiguous gene syndrome

troponin C and troponin I subunits

Cofactor binding induces a conformation change

FGF-19 Rabbit Polyclonal Antibody, 50ul[BT-AP10035] Molecular Biologyn MIM 610610)May be involved in brain development during embryogenesis. miscellaneous: Contrarily to other members of the family that can bind several FGF receptors FGF19 is specific for FGFR4. Belongs to the heparin binding growth factors family. tissue specificity: Expressed in fetal brain cartilage retina and adult gall bladder.