PRPS1 anticorps (AA 1-318)

N° du produit ABIN7596089

Cet anticorps anti-PRPS1 Monoclonal Souris (Clone AT1E11) (ABIN7596089) détecte spécifiquement PRPS1 dans WB, ELISA, IF et ICC. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour PRPS1 anticorps (AA 1-318) (ABIN7596089)

Antigène: PRPS1 (phosphoribosyl Pyrophosphate Synthetase 1 (PRPS1))

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp PRPS1 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunocytochemistry (ICC)

Clone: AT1E11

Détail du produit anti-PRPS1 anticorps

Épitope: AA 1-318

Fonction: Human PRPS1 antibody

Purification: Purified

Immunogène: Recombinant human PRPS1 (1-318aa) purified from E. coli

Isotype: IgG2a kappa

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: Phosphate-Buffered Saline ( pH 7.4) with 0.02 % Sodium Azide, 10 % glycerol

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.

Conseil sur la manipulation: Avoid repeated freezing and thawing cycles

Stock: 4 °C,-20 °C,-80 °C

Stockage commentaire: Can be stored at +2C to +8C for 1 week. For long term storage, aliquot and store at -20C to -80C. Avoid repeated freezing and thawing cycles.

Détails sur PRPS1

Antigène: PRPS1 (phosphoribosyl Pyrophosphate Synthetase 1 (PRPS1))

Autre désignation: PRPS1

Sujet: PRPS1 is an enzyme that catalyzes the phosphoribosylation of ribose 5-phosphate to 5-phosphoribosyl-1-pyrophosphate, which is necessary for purine metabolism and nucleotide biosynthesis. A mutation in PRPS1 may result in PRPS superactivity, a disease characterized by gout and the overproductionof purine nucleotides, uric acid and PRPP. PRPS1 mutations can also lead to a reduction in PRPS1 activity resulting in ARTS syndrome or CMTX5 (Charcot-Marie-Tooth disease X-linked recessive type 5).

NCBI Accession: NP_002755

Pathways: Ribonucleoside Biosynthetic Process