Warehouse Overstock Promotion |  Save 10%  on Premium Lab Supplies |  Shop Now

Menu

This product has been added to the cart.

NPHP1 Polyclonal Antibody Reactivity Human

SKU: E-AB-53023-200

  • $ 55995
  • Save $ 4000


Request a Quote

NPHP1 Polyclonal Antibody Reactivity Human

 

SKU # E-AB-53023
Reactivity Human, Mouse
Host Rabbit
Applications WB, IHC

 

Product Details

Isotype IgG
Host Rabbit
Reactivity Human, Mouse
Applications WB, IHC
Clonality Polyclonal
Immunogen Fusion protein of human NPHP1
Abbre NPHP1
Synonyms JBTS4,  Juvenile nephronophthisis 1 protein,  NPH1,  NPHP1,  Nephrocystin 1,  Nephronophthisis,  SLSN1,  nephronophthisis 1 (juvenile)
Swissprot
Calculated MW 83 kDa
Observed MW Refer to figures
Cellular Localization Cell junction, adherens junction. Cell projection, cilium. Cytoplasm, cytoskeleton, cilium axoneme. Cell junction, tight junction.
Concentration 1.02 mg/mL
Buffer Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
Purification Method Antigen affinity purification
Research Areas Cell Biology,  Signal transduction
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping The product is shipped with ice pack, upon receipt, store it immediately at the temperature recommended.

 

Related Reagents

Applications Recommended Dilution
WB 1:500-1:2000
IHC 1:50-1:300

 

Background

This gene encodes a protein with src homology domain 3 (SH3) patterns. This protein interacts with Crk-associated substrate, and it appears to function in the control of cell division, as well as in cell-cell and cell-matrix adhesion signaling, likely as part of a multifunctional complex localized in actin- and microtubule-based structures. Mutations in this gene cause familial juvenile nephronophthisis type 1, a kidney disorder involving both tubules and glomeruli. Defects in this gene are also associated with Senior-Loken syndrome type 1, also referred to as juvenile nephronophthisis with Leber amaurosis, which is characterized by kidney and eye disease, and with Joubert syndrome type 4, which is characterized by cerebellar ataxia, oculomotor apraxia, psychomotor delay and neonatal breathing abnormalities, sometimes including retinal dystrophy and renal disease. Multiple transcript variants encoding different isoforms have been found for this gene.