PGD anticorps (AA 40-120)

N° du produit ABIN7223134

L’anticorps Lapin Polyclonal anti-PGD a été validé pour WB et ELISA. Il convient pour détecter PGD dans des échantillons de Humain, Souris et Rat.

Aperçu rapide pour PGD anticorps (AA 40-120) (ABIN7223134)

Antigène: PGD (Phosphogluconate Dehydrogenase (PGD))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PGD est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-PGD anticorps

Épitope: AA 40-120

Fonction: PGD Polyclonal Antibody

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

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

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

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000). Not yet tested in other applications.

Commentaires:

Primary Antibody

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.

Agent conservateur: Sodium azide

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

Stock: -20 °C

Stockage commentaire: 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.

Détails sur PGD

Antigène: PGD (Phosphogluconate Dehydrogenase (PGD))

Autre désignation: PGD

Sujet: Rabbit Anti-PGD Polyclonal Antibody,PGD, PGDH, 6-phosphogluconate dehydrogenase, decarboxylating,6-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.,6-phosphogluconate dehydrogenase decarboxylating

Poids moléculaire: observerd band 40kDa

ID gène: 5226

UniProt: P52209