PRODH Antikörper (Center)

Produktnummer ABIN2855390

Der Kaninchen Polyklonal Anti-PRODH-Antikörper wurde für WB validiert. Er ist geeignet, PRODH in Proben von Human zu detektieren.

Kurzübersicht für PRODH Antikörper (Center) (ABIN2855390)

Target: PRODH (Proline Dehydrogenase (Oxidase) 1 (PRODH))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PRODH Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-PRODH Antikörper

Bindungsspezifität: Center

Kreuzreaktivität: Maus, Ratte (Rattus), Rind (Kuh)

Kreuzreaktivität (Details): Mouse (84 %), Rat (83 %), Bovine (80 %)

Produktmerkmale: Rabbit Polyclonal antibody to PRODH (proline dehydrogenase (oxidase) 1)
PRODH antibody [N1N3]

Aufreinigung: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the center region of human PRODH. The exact sequence is proprietary.

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Suggested dilution Reference Western blot 1:500-1:3000* Not tested in other applications. *Optimal dilutions/concentrations should be determined by the researcher.Suggested dilutionReferenceWestern blot1:500-1:3000*

Kommentare:

Positive Control: 293T

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: 1XPBS, 1 % BSA, 20 % Glycerol ( pH 7). 0.01 % Thimerosal was added as a preservative.

Konservierungsmittel: Thimerosal (Merthiolate)

Vorsichtsmaßnahmen: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Keep as concentrated solution. Aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Details zu PRODH

Target: PRODH (Proline Dehydrogenase (Oxidase) 1 (PRODH))

Andere Bezeichnung: PRODH

Hintergrund: The protein encoded by this gene is a mitochondrial proline dehydrogenase that catalyzes the first step in proline degradation. Defects in this gene are a cause of hyperprolinemia type 1 and possibly susceptibility to schizophrenia 4 (SCZD4). The gene is located on chromosome 22q11.21, a region which has also been associated with the contiguous gene deletion syndromes DiGeorge syndrome and CATCH22 syndrome.

Cellular Localization: Mitochondrion matrix

Molekulargewicht: 68 kDa

Gen-ID: 5625

Pathways: Response to Water Deprivation, Monocarboxylic Acid Catabolic Process