Liver Arginase Antikörper (AA 1-292)

Produktnummer ABIN1885889

Der Kaninchen Polyklonal Anti-Liver Arginase-Antikörper wurde für WB, IHC und IF validiert. Er ist geeignet, Liver Arginase in Proben von Human zu detektieren.

Kurzübersicht für Liver Arginase Antikörper (AA 1-292) (ABIN1885889)

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

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Liver Arginase Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)

Produktdetails anti-Liver Arginase Antikörper

Bindungsspezifität: AA 1-292

Aufreinigung: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 292 of arginase I

Anwendungsinformationen

Applikationshinweise: Suggested dilutions:
Western blotting: 1.500-1.3000
Immunohistochemistry: 1.100-1.500
Immunofluorescence: 1.100-1.200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

Konservierungsmittel: Thimerosal (Merthiolate)

Vorsichtsmaßnahmen: Biohazard Informations: This product contains thimerosal which is hazardous.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.

Details zu Liver Arginase

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

Andere Bezeichnung: arginase I

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 encoded by this gene, 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.[provided by RefSeq]

Molekulargewicht: 35 kDa

Gen-ID: 383

NCBI Accession: NM_000045, NP_000036

Pathways: Cellular Response to Molecule of Bacterial Origin