Phenylalanine Hydroxylase Antikörper (C-Term)

Produktnummer ABIN7216436

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch Phenylalanine Hydroxylase in WB, IHC, ELISA und IF. Es zeigt Reaktivität gegenüber Proben von Human, Maus und Ratte.

Kurzübersicht für Phenylalanine Hydroxylase Antikörper (C-Term) (ABIN7216436)

Target: Phenylalanine Hydroxylase

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Phenylalanine Hydroxylase Antikörper ist unkonjugiert

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

Produktdetails anti-Phenylalanine Hydroxylase Antikörper

Bindungsspezifität: C-Term

Verwendungszweck: Rabbit Anti-PAH Polyclonal Antibody

Spezifität: PAH Polyclonal Antibody detects endogenous levels of PAH protein.

Aufreinigung: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: Synthesized peptide derived from the C-terminal region of human PAH

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-1:2000,IHC 1:100-1:300,ELISA 1:40000,IF 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Haltbarkeit: 12 months

Details zu Phenylalanine Hydroxylase

Target: Phenylalanine Hydroxylase

Andere Bezeichnung: PAH

Hintergrund: PAH, Phenylalanine-4-hydroxylase, PAH, Phe-4-monooxygenasePAH encodes the enzyme phenylalanine hydroxylase that is the rate-limiting step in phenylalanine catabolism. Deficiency of this enzyme activity results in the autosomal recessive disorder phenylketonuria.

Molekulargewicht: 51kD

Gen-ID: 5053

UniProt: P00439