Nephrin (NPHS1) Mouse Monoclonal Antibody [Clone ID: OTI12D7]
Frequently bought together (2)
Transient overexpression lysate of nephrosis 1, congenital, Finnish type (nephrin) (NPHS1)
USD 605.00
Other products for "NPHS1"
Specifications
Product Data | |
Clone Name | OTI12D7 |
Applications | WB |
Recommended Dilution | WB 1:1000 |
Reactivities | Human |
Host | Mouse |
Isotype | IgG1 |
Clonality | Monoclonal |
Immunogen | Human recombinant protein fragment corresponding to amino acids 1077-1241 of human NPHS1 (NP_004637) produced in E.coli. |
Formulation | PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide. |
Concentration | 1 mg/ml |
Purification | Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G) |
Conjugation | Unconjugated |
Storage | Shipped at -20°C or with ice packs, Upon delivery store at -20°C. Dilute in PBS(pH7.3) if necessary. Stable for 12 months from date of receipt. Avoid repeated freeze-thaws. |
Stability | Stable for 12 months from date of receipt. |
Predicted Protein Size | 134.6 kDa |
Gene Name | NPHS1 nephrin |
Database Link | |
Background | 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.[provided by RefSeq, Oct 2009] |
Synonyms | CNF; nephrin; NPHN |
Reference Data | |
Protein Families | Druggable Genome, Transmembrane |
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