PRODH anticorps (AA 141-240)

N° du produit ABIN715136

L’anticorps Lapin Polyclonal anti-PRODH a été validé pour WB, ELISA, IF (cc), IF (p), IHC (p) et IHC (fro). Il convient pour détecter PRODH dans des échantillons de Souris et Rat.

Aperçu rapide pour PRODH anticorps (AA 141-240) (ABIN715136)

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

Reactivité: Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PRODH est non-conjugé

Application: Western Blotting (WB), ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Détail du produit anti-PRODH anticorps

Épitope: AA 141-240

Réactivité croisée: Souris, Rat

Homologie: Human,Horse

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human PRODH

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

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

Stock: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur PRODH

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

Autre désignation: PRODH

Sujet:

Synonyms: POX, PIG6, HSPOX2, PRODH1, PRODH2, TP53I6, Proline dehydrogenase 1, mitochondrial, Proline oxidase, Proline oxidase 2, p53-induced gene 6 protein, PRODH, POX2

Background: Proline oxidase catalyzes the conversion of proline to pyrroline-5-carboxylate, or P5C during the degradation of the amino acid Proline. Defects in PRODH are the cause of hyperprolinemia type 1, a disorder characterized by elevated serum proline levels. Defective PRODH may be involved in the psychiatric and behavioral phenotypes associated with the 22q11 velocardiofacial and DiGeorge syndrome and may be associated with susceptibility to schizophrenia 4 (SCZD4).

ID gène: 5625

UniProt: O43272

Pathways: Response to Water Deprivation, Monocarboxylic Acid Catabolic Process