UPB1 anticorps

N° du produit ABIN2462585

L’anticorps Lapin Polyclonal anti-UPB1 a été validé pour WB et ELISA. Il convient pour détecter UPB1 dans des échantillons de Humain, Souris, Rat, Chien, Poisson zèbre (Danio rerio), Drosophila melanogaster, Arabidopsis et C. elegans.

Aperçu rapide pour UPB1 anticorps (ABIN2462585)

Antigène: UPB1 (Ureidopropionase, beta (UPB1))

Reactivité: Humain, Souris, Rat, Chien, Poisson zèbre (Danio rerio), Drosophila melanogaster, Arabidopsis, C. elegans

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp UPB1 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-UPB1 anticorps

Purification: Antibody is purified by protein A chromatography method.

Immunogène: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human UPB1.

Information d'application

Indications d'application: UPB1 antibody can be used for detection of UPB1 by ELISA at 1:1562500. UPB1 antibody can be used for detection of UPB1 by western blot at 2.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Concentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Conseil sur la manipulation: As with any antibody avoid repeat freeze-thaw cycles.

Stock: 4 °C/-20 °C

Stockage commentaire: For short periods of storage (days) store at 4 °C. For longer periods of storage, store UPB1 antibody at -20 °C.

Détails sur UPB1

Antigène: UPB1 (Ureidopropionase, beta (UPB1))

Autre désignation: UPB1

Sujet: UPB1 is 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 activityThis 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.

Poids moléculaire: 42 kDa

ID gène: 51733

NCBI Accession: NP_057411

UniProt: Q9UBR1