Description: A polyclonal antibody raised in Rabbit that recognizes and binds to Human NPHP1 / Nephronophthisis . This antibody is tested and proven to work in the following applications:

Description: Rabbit polyclonal NPHP1 antibody

Description: A polyclonal antibody against NPHP1. Recognizes NPHP1 from Human. This antibody is Unconjugated. Tested in the following application: ELISA, IHC, IF; Recommended dilution: IHC:1:20-1:200, IF:1:50-1:200

Description: 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.

Description: Unconjugated Rabbit polyclonal to NPHP1

Description: A polyclonal antibody against NPHP1. Recognizes NPHP1 from Human. This antibody is HRP conjugated. Tested in the following application: ELISA

Description: A polyclonal antibody against NPHP1. Recognizes NPHP1 from Human. This antibody is FITC conjugated. Tested in the following application: ELISA