Nephrin Polyclonal Antibody, 20ul Miscellaneous The product of this gene

The product of this gene contains several domains similar to von Willebrand Factor type A domains

Mutations in FMN2 have been associated with mental retardation autosomal recessive 47 (MRT47)

which closely fits the reservoirs and can effectively reduce evaporation and contamination during incubation and storage

The expression of this receptor in lymphatic endothelial cells and overexpression in vascular tumors suggested its function in chemokine-driven recirculation of leukocytes and possible chemokine effects on the development and growth of vascular tumors

and they activate or interact with various endogenous or exogenous ligands

Nephrin Polyclonal Antibody, 20ul Miscellaneous The product of this geneNPHS1 encodes a member of the immunoglobulin family of cell adhesion molecules that functions in the glomerular filtration barrier in the kidney. NPHS1 is primarily expressed in renal tissues, and the protein is a type 1 transmembrane protein found at the slit diaphragm of glomerular podocytes. The slit diaphragm is thought to function as an ultrafilter to exclude albumin and other plasma macromolecules in the formation of urine. Mutations in this