UPB1 Antikörper
Kurzübersicht für UPB1 Antikörper (ABIN2462585)
Target
Alle UPB1 Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
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                                            Aufreinigung
- Antibody is purified by protein A chromatography method.
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                                            Immunogen
- Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human UPB1.
 
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                                            Applikationshinweise
- 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.
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                                            Beschränkungen
- Nur für Forschungszwecke einsetzbar
 
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                                            Format
- Lyophilized
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                                            Rekonstitution
- Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.
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                                            Konzentration
- 1 mg/mL
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                                            Buffer
- Antibody is lyophilized in PBS buffer with 2 % sucrose.
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                                            Handhabung
- As with any antibody avoid repeat freeze-thaw cycles.
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                                            Lagerung
- 4 °C/-20 °C
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                                            Informationen zur Lagerung
- 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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    - UPB1 (Ureidopropionase, beta (UPB1))
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                                            Andere Bezeichnung
- UPB1
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                                            Hintergrund
- 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.
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                                            Molekulargewicht
- 42 kDa
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                                            Gen-ID
- 51733
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                                            NCBI Accession
- NP_057411
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                                            UniProt
- Q9UBR1
 Target
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