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Nephrosis 1, Congenital, Finnish Type (Nephrin) Proteins (NPHS1)

NPHS1 encodes a member of the immunoglobulin family of cell adhesion molecules that functions in the glomerular filtration barrier in the kidney. Additionally we are shipping Nephrin Antibodies (199) and Nephrin Kits (47) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
NPHS1 4868 O60500
NPHS1 64563 Q9R044
NPHS1 54631 Q9QZS7
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Top Nephrin Proteins at antibodies-online.com

Showing 10 out of 16 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
HOST_Escherichia coli (E. coli) Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 29 to 34 Days
$4,331.68
Details
HOST_Escherichia coli (E. coli) Mouse His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 29 to 34 Days
$4,331.68
Details
Insect Cells Mouse rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.25 mg Log in to see 69 to 74 Days
$9,050.32
Details
Insect Cells Human rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.5 mg Log in to see 69 to 74 Days
$12,906.52
Details
HOST_Escherichia coli (E. coli) Human His tag 50 μg Log in to see 21 to 26 Days
$341.00
Details
HOST_Escherichia coli (E. coli) Human His tag,T7 tag 100 μg Log in to see 11 to 13 Days
$662.20
Details
HOST_Escherichia coli (E. coli) Rat His tag,GST tag 100 μg Log in to see 11 to 13 Days
$735.90
Details
HOST_Wheat germ Human GST tag 10 μg Log in to see 9 Days
$405.71
Details
HOST_Escherichia coli (E. coli) Mouse Un-conjugated 100 μg Log in to see 11 to 13 Days
$704.00
Details
HOST_Escherichia coli (E. coli) Human Un-conjugated   100 μg Log in to see 9 to 19 Days
$841.86
Details

NPHS1 Proteins by Origin and Source

Origin Expressed in Conjugate
Human , ,
, , ,
Rat (Rattus)

Mouse (Murine) ,
,

More Proteins for Nephrosis 1, Congenital, Finnish Type (Nephrin) (NPHS1) Interaction Partners

Zebrafish Nephrosis 1, Congenital, Finnish Type (Nephrin) (NPHS1) interaction partners

  1. Nephrin signal bordered the lateral membrane of podocytes, which were columnar in shape

  2. Using two models, zebrafish and mice, that the absence of nephrin results in poorly developed muscles and incompletely fused myotubes, respectively.

Human Nephrosis 1, Congenital, Finnish Type (Nephrin) (NPHS1) interaction partners

  1. there is a link found of the glomerular protein nephrin and the antihypertensive action of angiotensin receptor antagonists in the treatment of hypertension.

  2. A novel nonsense mutation in NPHS1 linking aortic stenosis associated with congenital nephropathy, is reported.

  3. Activated IQGAP1, as an intracellular partner of nephrin, is involved in actin cytoskeleton organization and functional regulation of podocytes.

  4. NPHS1 rs437168 variant is associated with nephrotic syndrome in children.

  5. biochemical reconstitution on supported lipid bilayers of protein clusters containing the adhesion receptor Nephrin and its cytoplasmic partners, Nck (show NCK1 Proteins) and N-WASP (show WASL Proteins), is reported.

  6. Coding variants in NPHS1 are associated with both risk for and protection from common forms of nephropathy in African Americans.

  7. Phosphorylation of nephrin is important for the survival status of podocytes.

  8. No pathogenic NPHS1 mutations were found in the cohort of children with steroid-resistant focal segmental glomerulosclerosis.

  9. Proteinuria in patients with seropositive rheumatoid arthritis is associated with increased levels of urine nephrin excretion, the highest levels of nephrin excretion were registered in patients with glomerulonephritis and amyloidosis.

  10. the frequency of identified disease causing mutations (NPHS1 and NPHS2) in children with steroid-resistant nephrotic syndome is 11.4%, and they show no response to treatment.

Mouse (Murine) Nephrosis 1, Congenital, Finnish Type (Nephrin) (NPHS1) interaction partners

  1. interaction of full-length suPAR with alphavbeta3 integrin expressed on podocytes results in down-modulation of nephrin that may affect kidney functionality in different human pathologies characterized by increased concentration of suPAR.

  2. Nphs1 is an activity dependent gene in mouse olfactory sensory neurons.

  3. ACE2 (show ACE2 Proteins) deficiency exacerbates kidney inflammation, oxidative stress and adverse renal injury in the ApoE (show APOE Proteins)-mutant mice through modulation of the nephrin, NOX4 (show NOX4 Proteins) and TNF-alpha (show TNF Proteins)-TNFRSF1A (show TNFRSF1A Proteins) signaling.

  4. Nephrin is involved in pancreatic beta-cell survival signaling; a marked decrease in nephrin expression and phosphorylated Akt (show AKT1 Proteins) was observed in pancreatic islets of leptin receptor (show LEPR Proteins)-deficient diabetic mice.

  5. SHP-1 (show PTPN6 Proteins) contributes to nephrin deactivation in podocytes exposed to high glucose levels.

  6. The aPKC-Par3 (show F2RL2 Proteins) complex regulates the cell-surface localization of nephrin.

  7. A novel direct interaction between the Sema3a (show SEMA3A Proteins) signaling receptor plexinA1 (show PLXNA1 Proteins) and nephrin, linking extracellular Sema3a (show SEMA3A Proteins) signals to the slit-diaphragm signaling complex, was identified.

  8. The planar cell polarity pathway contributes to podocyte development by regulating nephrin turnover during junctional remodeling as the cells differentiate.

  9. Robo2 (show ROBO2 Proteins) signaling acts as a negative regulator on nephrin to influence podocyte foot process architecture.

  10. Notch (show NOTCH1 Proteins) signaling induces endocytosis of nephrin, thereby triggering the onset of proteinuria.

Nephrin (NPHS1) Protein Profile

Protein Summary

This gene encodes a member of the immunoglobulin family of cell adhesion molecules that functions in the glomerular filtration barrier in the kidney. The gene 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 gene result in Finnish-type congenital nephrosis 1, characterized by severe proteinuria and loss of the slit diaphragm and foot processes.

Gene names and symbols associated with NPHS1

  • nephrosis 1, congenital, Finnish type (nephrin) (NPHS1)
  • nephrosis 1, congenital, Finnish type (nephrin) (nphs1)
  • nephrin (nphs1)
  • nephrin (AaeL_AAEL003853)
  • nephrosis 1, congenital, Finnish type (nephrin) (Nphs1)
  • nephrosis 1, nephrin (Nphs1)
  • CNF protein
  • nephrin protein
  • NephrinB protein
  • NPHN protein
  • nphs1 protein
  • nphs1l protein

Protein level used designations for NPHS1

nephrosis 1, congenital, Finnish type (nephrin) , nephrin , renal glomerulus-specific cell adhesion receptor , nephrosis 1 homolog, nephrin , nephrin 1

GENE ID SPECIES
468841 Pan troglodytes
692352 Danio rerio
734213 Xenopus laevis
5579127 Aedes aegypti
4868 Homo sapiens
64563 Rattus norvegicus
100354996 Oryctolagus cuniculus
100713185 Cavia porcellus
100622946 Sus scrofa
484571 Canis lupus familiaris
519706 Bos taurus
101115895 Ovis aries
54631 Mus musculus
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