Renin anticorps

N° du produit ABIN7882151

Cet anticorps anti-Renin Polyclonal Lapin (ABIN7882151) détecte spécifiquement Renin dans IHC (p). L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour Renin anticorps (ABIN7882151)

Antigène: Renin (REN)

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Renin est non-conjugé

Application: Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-Renin anticorps

Fonction: Renin Antibody / REN

Séquence: RKFYTEFDRR NNRIGFALAR

Purification: Affinity purified

Immunogène: Amino acids RKFYTEFDRRNNRIGFALAR from the human protein were used as the immunogen for the Renin antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the Renin antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the Renin antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur Renin

Antigène: Renin (REN)

Autre désignation: Renin

Sujet: The REN gene encodes Renin, an aspartic protease that is secreted by the kidneys. Renin is a part of the renin-angiotensin-aldosterone system involved in regulation of blood pressure, and electrolyte balance. This enzyme catalyzes the first step in the activation pathway of angiotensinogen by cleaving angiotensinogen to form angiotensin I, which is then converted to angiotensin II by angiotensin I converting enzyme. This cascade can result in aldosterone release, narrowing of blood vessels, and increase in blood pressure as angiotension II is a vasoconstrictive peptide. Transcript variants that encode different protein isoforms and that arise from alternative splicing and the use of alternative promoters have been described, but their full-length nature has not been determined. Mutations in this gene have been shown to cause hyperuricemic nephropathy familial juvenile 2, familial hyperproreninemia, and renal tubular dysgenesis.

UniProt: P00797

Pathways: ACE Inhibitor Pathway, Peptide Hormone Metabolism, Regulation of Systemic Arterial Blood Pressure by Hormones, Feeding Behaviour