FGF-19 Rabbit Polyclonal Antibody, 50ul[BT-AP10035] Molecular Biologyn Possibly via autoubiquitination

Possibly via autoubiquitination

Cofactor binding induces a conformation change

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

FGF-19 Rabbit Polyclonal Antibody, 50ul[BT-AP10035] Molecular Biologyn Possibly via autoubiquitinationMay 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.