N-cadherin Polyclonal Antibody, 20ul Protein Post-translational Modification a rare autosomal dominant proximal

a rare autosomal dominant proximal myopathy with early childhood onset

has been shown to regulate glucose homeostasis

The encoded protein (mannan binding lectin serine peptidase 1) is synthesized as a zymogen and is activated when it complexes with the pathogen recognition molecules of lectin pathway

The encoded protein circulates in the plasma and is involved with metabolic and hormonal processes

2001 [PubMed 12063393])

N-cadherin Polyclonal Antibody, 20ul Protein Post-translational Modification a rare autosomal dominant proximalCDH2 encodes a classical cadherin and member of the cadherin superfamily. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein is proteolytically processed to generate a calcium dependent cell adhesion molecule and glycoprotein. Cadherin 2 plays a role in the establishment of left right asymmetry, development of the nervous system and the formation of cartilage and bone.