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Anti-UPB1 Rabbit Polyclonal Antibody
Anti-UPB1 Rabbit Polyclonal Antibody
Catalog #: 10108-964
Supplier:  Prosci
UPB1 antibody
Anti-UPB1 Rabbit Polyclonal Antibody
Catalog #: 10108-964
Supplier:  Prosci
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Specifications

  • Antibody type:
    Primary
  • Antigen name:
    ureidopropionase, beta
  • Clonality:
    Polyclonal
  • Gene ID:
    Q9UBR1
  • Host:
    Rabbit
  • Reactivity:
    Zebrafish,
    Drosophila,
    Arabidopsis,
    C. elegans,
    Human,
    Dog,
    Rat,
    Mouse
  • Antigen symbol:
    UPB1
  • Conjugation:
    Unconjugated
  • ELISA:
    Yes
  • Size:
    100 ul
  • Western blot:
    Yes
  • Form:
    Liquid
  • Antigen synonyms:
    UPB1
  • Storage buffer:
    Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
  • Molecular weight:
    42 kDa
  • Storage temperature:
    For short periods of storage (days) store at 4 °C. For longer periods of storage, store UPB1 antibody at –20 °C. As with any antibody avoid repeat freeze-thaw cycles.
  • Shipping temperature:
    4 °C
  • Immunogen:
    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human UPB1.
  • Purification:
    Antibody is purified by protein A chromatography method.
  • Cat. no.:
    10108-964
  • Supplier No.:
    29-755

Specifications

About this item

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.

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 ?g/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Antibody is purified by protein A chromatography method.

Antibody is lyophilized in PBS buffer with 2% sucrose. Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Type: Primary
Antigen: UPB1
Clonality: Polyclonal
Clone:
Conjugation: Unconjugated
Epitope:
Host: Rabbit
Isotype:
Reactivity: Human, Mouse, Rat, Dog, Drosophila, Zebrafish, Arabidopsis, C. elegans

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