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Invitrogen™ Nephrin Monoclonal Antibody (C8)

Mouse Monoclonal Antibody

Supplier:  Invitrogen™ MA543718

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Catalog No. PIMA543718


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Description

Description

Nephrin Monoclonal Antibody for Western Blot, ICC/IF

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.
TRUSTED_SUSTAINABILITY
Specifications

Specifications

Nephrin
Monoclonal
1 mg/mL
PBS with 50% glycerol and 0.05% ProClin 300
O60500
Nphs1
Recombinant protein Nephrin. The antigen corresponds to amino acid range 27-234 of the target protein.
20 μL
Primary
Human
Antibody
IgG2a κ
Western Blot, Immunocytochemistry, Western Blot
C8
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
Mouse
Protein A/G
RUO
4868
-20°C
Liquid
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