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Proteintech

Nephrin Monoclonal Antibody (1D11H8)

4 References
View all (24) Nephrin antibodies

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Datasheet
Protocols
Questions & Answers
Datasheet
Protocols
Questions & Answers

Cite Nephrin Monoclonal Antibody (1D11H8)

  • Antibody Testing Data (2)
Nephrin Antibody in Immunohistochemistry (Paraffin) (IHC (P))
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Nephrin Antibody in Immunohistochemistry (Paraffin) (IHC (P))
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FIGURE: 1 / 2

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Nephrin Antibody (66970-1-IG) in IHC (P)

Immunohistochemical analysis of paraffin-embedded human kidney tissue slide using 66970-1-Ig (Nephrin antibody) at dilution of 1:4000 (under 40x lens. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). {{ $ctrl.currentElement.advancedVerification.fullName }} validation info. View more
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Nephrin Antibody in Immunohistochemistry (Paraffin) (IHC (P))
Nephrin Antibody in Immunohistochemistry (Paraffin) (IHC (P))

Product Details

66970-1-IG

Applications
Tested Dilution
Publications

Western Blot (WB)

-
View 3 publications 3 publications

Immunohistochemistry (Paraffin) (IHC (P))

1:4,000
-

Immunocytochemistry (ICC/IF)

-
View 1 publication 1 publication
Product Specifications

Species Reactivity

Human

Host/Isotype

Mouse / IgG1

Class

Monoclonal

Type

Antibody

Clone

1D11H8

Immunogen

NPHS1 Fusion Protein Ag19273

Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

1000 µg/mL

Purification

Protein G

Storage buffer

PBS, pH 7.3, with 50% glycerol

Contains

0.02% sodium azide

Storage conditions

-20°C

Shipping conditions

Wet ice

Product Specific Information

Aliquoting is unnecessary for -20°C storage.

Target Information

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.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

Bioinformatics

Protein Aliases: Nephrin; nephrosis 1, congenital, Finnish type (nephrin); NPHS1 nephrin; Renal glomerulus-specific cell adhesion receptor

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Gene Aliases: CNF; nephrin; NPHN; NPHS1

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UniProt ID: (Human) O60500

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Entrez Gene ID: (Human) 4868

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Function(s)
protein binding myosin binding
Process(es)
cell adhesion JNK cascade skeletal muscle tissue development myoblast fusion excretion positive regulation of actin filament polymerization glomerular basement membrane development protein localization to synapse regulation of excretion glomerular visceral epithelial cell development
It has to be done as per old AB suggested Products section.
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