PC11X Rabbit Polyclonal Antibody, 100ul Enzymes disease:Defects in COL5A1 are a

disease:Defects in COL5A1 are a cause of Ehlers-Danlos syndrome type 1 (EDS1)

expression of the FOS gene has also been associated with apoptotic cell death

The activity of this receptor may stimulate alpha gustducin

Activity of this protein is key in the development of neural tissues| particularly the eye

PC11X Rabbit Polyclonal Antibody, 100ul Enzymes disease:Defects in COL5A1 are aThis gene belongs to the protocadherin gene family a subfamily of the cadherin superfamily. The encoded protein consists of an extracellular domain containing 7 cadherin repeats a transmembrane domain and a cytoplasmic tail that differs from those of the classical cadherins. The gene is located in a major X Y block of homology and its Y homolog despite divergence leading to coding region changes is the most closely related cadherin family member. The