GPR143 Polyclonal Antibody, 50ul Protein Post-translational Modification Some patients with Ehlers-Danlos syndrome

Some patients with Ehlers-Danlos syndrome type VI have deficiencies in lysyl hydroxylase activity

Alternatively spliced transcript variants encoding different isoforms have been found for MDM1

This gene encodes the beta subunit of follicle-stimulating hormone

The interaction of this protein with TRADD

The product of this gene typically dimerizes with keratin 18 to form an intermediate filament in simple single-layered epithelial cells

GPR143 Polyclonal Antibody, 50ul Protein Post-translational Modification Some patients with Ehlers-Danlos syndromeGPR143 encodes a protein that binds to heterotrimeric G proteins and is targeted to melanosomes in pigment cells. This protein is thought to be involved in intracellular signal transduction mechanisms. Mutations in GPR143 cause ocular albinism type 1, also referred to as Nettleship Falls type ocular albinism, a severe visual disorder. A related pseudogene has been identified on chromosome Y.