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Nephrin Polyclonal Antibody, 50ul Culture Media This syndrome is characterized by

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Nephrin Polyclonal Antibody, 50ul Culture Media This syndrome is characterized byNPHS1 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

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Description

This syndrome is characterized by a profuse sweating after exposure to cold as well as congenital physical abnormalities of the head and spine

The protein encoded by this gene is the CD3-gamma polypeptide

This gene may be associated with autism spectrum disorder in human patients

TCF25 is a member of the basic helix-loop-helix (bHLH) family of transcription factors that are important in embryonic development (Steen and Lindholm

Golgi reassembly-stacking protein 2 also plays a role in the intracellular transport of transforming growth factor alpha and may function as a molecular chaperone

Nephrin Polyclonal Antibody, 50ul Culture Media This syndrome is characterized byNPHS1 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

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