UPB1 anticorps
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- Antigène Voir toutes UPB1 Anticorps
- UPB1 (Ureidopropionase, beta (UPB1))
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Reactivité
- Humain, Souris, Rat, Chien, Poisson zèbre (Danio rerio), Drosophila melanogaster, Arabidopsis, C. elegans
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp UPB1 est non-conjugé
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Application
- Western Blotting (WB), ELISA
- 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.
- Top Product
- Discover our top product UPB1 Anticorps primaire
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- 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
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- 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.
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- Antigène
- UPB1 (Ureidopropionase, beta (UPB1))
- Autre désignation
- UPB1 (UPB1 Produits)
- Synonymes
- anticorps MGC82230, anticorps wu:fb69e03, anticorps zgc:64020, anticorps BUP1, anticorps AI195023, anticorps Bup1, anticorps ureidopropionase, beta S homeolog, anticorps beta-ureidopropionase 1, anticorps ureidopropionase, beta, anticorps UreidoPropionase Beta, anticorps upb1.S, anticorps UPB1, anticorps upb1, anticorps upb-1, anticorps 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
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