UPB1 anticorps

N° du produit ABIN8125614

L’anticorps anti-UPB1 Monoclonal Lapin est utilisé pour la détection de UPB1 dans des échantillons de Humain. Il a été validé pour WB, IHC et IP.

Aperçu rapide pour UPB1 anticorps (ABIN8125614)

Antigène: UPB1 (Ureidopropionase, beta (UPB1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Monoclonal

Conjugué: Cet anticorp UPB1 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), Immunoprecipitation (IP)

Clone: AB2247

Détail du produit anti-UPB1 anticorps

Fonction: UPB1 Rabbit mAb

Specificité: This antibody detects endogenous levels of UPB1 protein.

Purification: The antibody was purified by protein A affinity chromatography.

Immunogène: Recombinant protein (or fragment).

Isotype: IgG

Information d'application

Indications d'application: WB, 1:1000-1:5000 | IHC, 1:•100-1:300 | IP, 0. 5 μg-4 μg antibody for 200 μg-400 μg extracts of whole cells. |

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: The antibody is provided in liquid form in phosphate - buffered saline with 50 % glycerol, 0.05 % BSA, and 0.05 % Proclin 300.

Agent conservateur: ProClin

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

Conseil sur la manipulation: Avoid freeze / thaw cycles

Stock: -20 °C

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

Détails sur UPB1

Antigène: UPB1 (Ureidopropionase, beta (UPB1))

Autre désignation: UPB1

Sujet:

Synonyms: UPB1, BUP1, Beta-ureidopropionase , BUP-1, Beta-alanine synthase, N-carbamoyl-beta-alanine amidohydrolase,

Background: This gene encodes a protein that belongs to the CN hydrolase family. Beta-ureidopropionase catalyzes the last step in the pyrimidine degradation pathway. The pyrimidine bases uracil and thymine are degraded via the consecutive action of dihydropyrimidine dehydrogenase (DHPDH) , dihydropyrimidinase (DHP) and beta-ureidopropionase (UP) to beta-alanine and beta-aminoisobutyric acid, respectively. UP deficiencies are associated with N-carbamyl-beta-amino aciduria and may lead to abnormalities in neurological activity. [provided by RefSeq, Jul 2008]

Gene Name: UPB1, BUP1

Protein Name: UPB1

ID gène: 51733

UniProt: Q9UBR1