Podocin/NPHS2 Antibody

NPHS2 encodes the glomerular protein podocin which plays a role in the regulation of glomerular permeability, and acts as a linker between the plasma membrane and the cytoskeleton. Defects in this gene are the cause of autosomal recessive steroid-resistant nephrotic syndrome (SRN). SRN is characterized by onset between three months and five years, resistance to steroid therapy and rapid progression to end-stage renal disease. An alternative splice variant has been described but its full length sequence has not been determined. [provided by RefSeq]

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

We have publications tested in 1 confirmed species: Mouse.

We have publications tested in 1 application: WB.

Showing Publications 1 - 3 of 3.

Publications using NBP2-26057	Applications	Species
Zhang F, Liu J, Yu J et al. Effect of Nephropathy Prescription I on the Expression of Angptl3 and Podocyte-Associated Protein in Mice with Adriamycin-Induced Nephropathy. Evidence-based complementary and alternative medicine : eCAM 2021-04-01 [PMID: 38149181]
Zhang F, Liu J, Yu J et al. Effect of Nephropathy Prescription I on the Expression of Angptl3 and Podocyte-Associated Protein in Mice with Adriamycin-Induced Nephropathy Evidence-Based Complementary and Alternative Medicine 2022-01-31 [PMID: 36787114] (WB, Mouse)	WB	Mouse
Relle M, Cash H, Brochhausen C et al. New perspectives on the renal slit diaphragm protein podocin. Mod Pathol 2011-08-01 [PMID: 21499232]

Array NBP2-26057

• Podocin/NPHS2 Antibodies
• Podocin/NPHS2 ELISA Kit
• Podocin/NPHS2 Lysate
• Podocin/NPHS2 Proteins
• Podocin/NPHS2 Proteins and Enzyme