Liver Arginase Antikörper (C-Term)

Produktnummer ABIN374812

Dieser Ziege Polyklonal Antikörper detektiert spezifisch Liver Arginase in WB. Es zeigt Reaktivität gegenüber Proben von Ratte und Maus.

Kurzübersicht für Liver Arginase Antikörper (C-Term) (ABIN374812)

Target: Liver Arginase (ARG1) (Arginase, Liver (ARG1))

Reaktivität: Ratte, Maus

Wirt: Ziege

Klonalität: Polyklonal

Konjugat: Dieser Liver Arginase Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-Liver Arginase Antikörper

Bindungsspezifität: C-Term

Sequenz: C-NHKPETDYLK PPK

Spezifität: This antibody detects Arginase-1.

Kreuzreaktivität (Details): Species reactivity (tested):Mouse, Rat.

Aufreinigung: Ammonium Sulphate Precipitation followed by Antigen Affinity Chromatography using the immunizing peptide

Immunogen: Peptide from the C-Terminus of the protein sequence according to NP_058830.2 Genename: Arg1

Anwendungsinformationen

Applikationshinweise: Peptide ELISA: antibody detection limit dilution 1: 32000. Western blot: 0.01-0.03 μg/mL. Approx 37 kDa band observed in Mouse Liver and Rat Liverlysates (calculated MW of 35.7 kDa according to NP_058830.1).
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 0.5 mg/mL

Buffer: Tris saline, pH ~7.3, 0.02 % Sodium Azide, 0.5 % BSA

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handhabung: Avoid repeated freezing and thawing.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Details zu Liver Arginase

Target: Liver Arginase (ARG1) (Arginase, Liver (ARG1))

Andere Bezeichnung: Arginase-1

Hintergrund: Arginase catalyzes the hydrolysis of Arginine to Ornithine and Urea. At least two isoforms of mammalian arginase exist (types I and II) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. The type I isoform, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia.Synonyms: ARG1, Liver-type arginase, Type I arginase

Gen-ID: 11846, 10090

UniProt: Q61176

Pathways: Cellular Response to Molecule of Bacterial Origin