PRODH anticorps (Center)

N° du produit ABIN2855390

L’anticorps Lapin Polyclonal anti-PRODH a été validé pour WB. Il convient pour détecter PRODH dans des échantillons de Humain.

Aperçu rapide pour PRODH anticorps (Center) (ABIN2855390)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PRODH est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-PRODH anticorps

Épitope: Center

Réactivité croisée: Souris, Rat (Rattus), Boeuf (Vache)

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

Attributs du produit: Rabbit Polyclonal antibody to PRODH (proline dehydrogenase (oxidase) 1)
PRODH antibody [N1N3]

Purification: Purified by antigen-affinity chromatography.

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

Isotype: IgG

Information d'application

Indications d'application: 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*

Commentaires:

Positive Control: 293T

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

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

Agent conservateur: Thimerosal (Merthiolate)

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

Stock: -20 °C

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

Détails sur PRODH

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

Autre désignation: PRODH

Sujet: 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

Poids moléculaire: 68 kDa

ID gène: 5625

Pathways: Response to Water Deprivation, Monocarboxylic Acid Catabolic Process