Uromodulin (UMOD) (C-Term) Peptide
Aperçu rapide pour Uromodulin (UMOD) (C-Term) Peptide (ABIN8115530)
Antigène
Origine
Source
Application
-
-
Protein Region
- C-Term
-
Fonction
- UMOD Peptide - C-terminal region
-
Séquence
- PTCSGTRFRS GSVIDQSRVL NLGPITRKGV QATVSRAFSS LGLLKVWLPL
-
-
Uromodulin (UMOD) peptide (Ovalbumin)
UMOD Reactivité: Humain Hôte: Synthetic WB, Imm, SDS
-
-
Indications d'application
- Optimal working dilution should be determined by the investigator.
-
Commentaires
-
This is a synthetic peptide designed for use in combination with anti-UMOD Antibody(ARP41437_P050),. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications. Please inquire for more details.
-
Restrictions
- For Research Use only
-
-
-
Format
- Lyophilized
-
Reconstitution
- Add 100 µL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
-
Buffer
- Lyophilized powder
-
Stock
- -20 °C
-
Stockage commentaire
- For longer periods of storage, store at -20 °C. Avoid repeat freeze-thaw cycles.
-
-
- Uromodulin (UMOD)
-
Sujet
-
Background Information: This gene encodes uromodulin, the most abundant protein in normal urine. Its excretion in urine follows proteolytic cleavage of the ectodomain of its glycosyl phosphatidylinosital-anchored counterpart that is situated on the luminal cell surface of the loop of Henle. Uromodulin may act as a constitutive inhibitor of calcium crystallization in renal fluids. Excretion of uromodulin in urine may provide defense against urinary tract infections caused by uropathogenic bacteria. Defects in this gene are associated with the autosomal dominant renal disorders medullary cystic kidney disease-2 (MCKD2) and familial juvenile hyperuricemic nephropathy (FJHN). These disorders are characterized by juvenile onset of hyperuricemia, gout, and progressive renal failure. While several transcript variants may exist for this gene, the full-length natures of only two have been described to date. These two represent the major variants of this gene and encode the same isoform.
Alternative Symbols: ADMCKD2, FJHN, HNFJ, HNFJ1, MCKD2, THGP, THP
-
Poids moléculaire
- 67kDa
-
ID gène
- 7369
-
NCBI Accession
- NP_001008390
-
UniProt
- P07911
Antigène
-
