PIPA5121510
UPB1 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA5121510-Each-of-1 | In Stock | ₹ 17,346.10 |
PIPA5121510 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 17,346.10
GST (18%): ₹ 3,122.298
Total Price: ₹ 20,468.398
Antigen
UPB1
Classification
Polyclonal
Conjugate
Unconjugated
Gene
UPB1
Gene Alias
AI195023; Beta-alanine synthase; beta-ureidopropionase; beta-ureidopropionase 1; BUP1; BUP-1; N-carbamoyl-beta-alanine amidohydrolase; UPB1; ureidopropionase, beta; wu:fb69e03; zgc:64020
Host Species
Rabbit
Purification Method
Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
51733
Content And Storage
-20°C
Form
Liquid
Applications
Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot
Concentration
500 μg/mL
Formulation
PBS with 50% glycerol and 0.05% ProClin 300
Gene Accession No.
Q9UBR1
Gene Symbols
UPB1
Immunogen
Recombinant protein Beta-ureidopropionase. The antigen corresponds to amino acid range 121-384 of the target protein.
Quantity
20 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG
Related Products
Description
- 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 activity
- 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.