PPOX anticorps

N° du produit ABIN7243778

Détail du produit anti-PPOX anticorps

Antigène: PPOX (Protoporphyrinogen Oxidase (PPOX))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PPOX est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), ELISA

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Synthetic peptide of human PPOX

Isotype: IgG

Information d'application

Indications d'application: WB 1:1000-1:5000, IHC 1:50-1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

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: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur PPOX

Antigène: PPOX (Protoporphyrinogen Oxidase (PPOX))

Autre désignation: PPOX (PPOX Produits)

Synonymes: anticorps PPO, anticorps V290M, anticorps VP, anticorps Ppo, anticorps BcDNA:LD41392, anticorps CG5796, anticorps Dmel\\CG5796, anticorps ESTS:9F2T, anticorps zgc:123252, anticorps HEMG1, anticorps PPO1, anticorps PROTOPORPHYRINOGEN OXIDASE, anticorps TC0121, anticorps hemG, anticorps protoporphyrinogen oxidase, anticorps Protoporphyrinogen oxidase, anticorps Flavin containing amine oxidoreductase family, anticorps polyphenol oxidase, chloroplastic, anticorps PPOX, anticorps Ppox, anticorps ppox, anticorps hemY, anticorps TC_RS00645, anticorps Mrub_1406, anticorps Mesil_2992, anticorps Trad_0583, anticorps Calni_0746, anticorps Ocepr_1049, anticorps Tmar_0766, anticorps Intca_1907, anticorps Despr_0642, anticorps Plabr_2407, anticorps Deipr_2130, anticorps Hipma_0622, anticorps LOC110782963

Sujet: This gene encodes the penultimate enzyme of heme biosynthesis, which catalyzes the 6-electron oxidation of protoporphyrinogen IX to form protoporphyrin IX. Mutations in this gene cause variegate porphyria, an autosomal dominant disorder of heme metabolism resulting from a deficiency in protoporphyrinogen oxidase, an enzyme located on the inner mitochondrial membrane. Alternatively spliced transcript variants encoding the same protein have been identified.

Poids moléculaire: 51 kDa

NCBI Accession: NP_000300

UniProt: P50336

Pathways: Synaptic Membrane, Feeding Behaviour