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Invitrogen™ Nephrin Polyclonal Antibody

Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA5109310
Description
Positive Control: Human kidney tissue, 293T, PANC-1, PC-12.
Primary steroid resistant nephrotic syndrome (SRNS) is characterized by childhood onset of proteinuria and progression to end stage renal disease. Kidney podocytes and their slit diaphragms form the final barrier to urinary protein loss. Congenital nephrotic syndrome (CNS) is caused by mutations in NPHS1 (nephrin) or NPHS2. Nephrin, a recently identified protein is a member of a group of podocyte proteins that constitute major component of the slit diaphragm especially in the foot process. Nephrin, a cell adhesion molecule, may play a crucial role in maintaining the glomerular filtration barrier. Recent studies have suggested that mutations in the gene for Nephrin reportedly lead to congenital nephrosis. Three novel podocyte proteins, Podocin, Nephrin and alpha Actinin 4 have been identified in congenital and experimental models of proteinuria. The role of Nephrin in anti apoptotic activity in podocyte slit diaphragm is believed to be associated with vascular endothelial derived growth factors VEGF signaling. Nephrin seems to play a role in the development or function of the kidney glomerular filtration barrier and it may anchor the podocyte slit diaphragm to the actin cytoskeleton.
Specifications
Nephrin | |
Polyclonal | |
Unconjugated | |
Nphs1 | |
CNF; Nephrin; nephrin 1; NephrinB; nephrosis 1 homolog, nephrin; nephrosis 1, congenital, Finnish type (nephrin); nephrosis 1, nephrin; NPHN; NPHS1; NPHS1 nephrin; NPHS1, nephrin; renal glomerulus-specific cell adhesion receptor | |
Rabbit | |
Affinity chromatography | |
RUO | |
4868 | |
-20°C, Avoid Freeze/Thaw Cycles, store in dark | |
Liquid |
Western Blot, Immunocytochemistry | |
1 mg/mL | |
PBS with 0.2% BSA, 50% glycerol and 0.05% sodium azide; pH 7.4 | |
O60500 | |
Nphs1 | |
Recombinant protein within Human Nephrin aa 1,042-1,241. | |
100 μL | |
Primary | |
Human | |
Antibody | |
IgG |
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