PGD Antikörper (AA 40-120)

Produktnummer ABIN7223134

Der Kaninchen Polyklonal anti-PGD Antikörper wird verwendet zum Nachweis von PGD in Proben von Human, Maus und Ratte. Er wurde validiert für WB, ELISA, IF und IHC.

Kurzübersicht für PGD Antikörper (AA 40-120) (ABIN7223134)

Target: PGD (Phosphogluconate Dehydrogenase (PGD))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PGD Antikörper ist unkonjugiert

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

Produktdetails anti-PGD Antikörper

Bindungsspezifität: AA 40-120

Verwendungszweck: Rabbit Anti-PGD Polyclonal Antibody

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

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

Immunogen: Synthesized peptide derived from the Internal region of human PGD at AA range: 40-120

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: IHC: 100-300,WB 1:500-1:2000,ELISA 1:5000,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 PGD

Target: PGD (Phosphogluconate Dehydrogenase (PGD))

Andere Bezeichnung: PGD

Hintergrund: PGD, PGDH, 6-phosphogluconate dehydrogenase, decarboxylating6-phosphogluconate dehydrogenase (PGD) is the second dehydrogenase in the pentose phosphate shunt. Deficiency of this enzyme is generally asymptomatic, and the inheritance of this disorder is autosomal dominant. Hemolysis results from combined deficiency of 6-phosphogluconate dehydrogenase and 6-phosphogluconolactonase suggesting a synergism of the two enzymopathies. Several transcript variants encoding different isoforms have been found for this gene.

Molekulargewicht: 40kD

Gen-ID: 5226

UniProt: P52209