K-cadherin Polyclonal Antibody, 100ul[BT-AP10599] Fluorescent Staining and a loss of function

and a loss of function mutation has been found in a kindred with a lymphedema-choanal atresia

|tissue specificity:Expressed in monocytes and mature macrophages such as Kupffer cells in the liver| red pulp macrophages in the spleen| cortical macrophages in the thymus| resident bone marrow macrophages and meningeal macrophages of the central nervous system

0 kb in adult lung

Capacity：50mL x 4

K-cadherin Polyclonal Antibody, 100ul[BT-AP10599] Fluorescent Staining and a loss of functionThis gene encodes a member of the cadherin superfamily. Cadherins are membrane glycoproteins that mediate homophilic cell cell adhesion and play critical roles in cell differentiation and morphogenesis. The encoded protein is a type II cadherin and may play a role in kidney development as well as endometrium and placenta formation. Decreased expression of this gene may be associated with tumor growth and metastasis.