Purine Nucleoside Phosphorylase Activity Assay Kit (Colorimetric) (ab204707)
Key features and details
- Assay type: Enzyme activity
- Detection method: Colorimetric
- Platform: Microplate reader
- Sample type: Cell Lysate, Purified protein, Tissue Lysate
Overview
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Product name
Purine Nucleoside Phosphorylase Activity Assay Kit (Colorimetric)
See all Nucleoside phosphorylase kits -
Detection method
Colorimetric -
Sample type
Cell Lysate, Purified protein, Tissue Lysate -
Assay type
Enzyme activity -
Species reactivity
Reacts with: Mammals, Other species -
Product overview
Purine Nucleoside Phosphorylase Activity Assay Kit (Colorimetric) (ab204707) is an assay where the hypoxanthine formed by the breakdown of inosine is further converted to uric acid using a developer. The uric acid is measured at a wavelength of OD=293 nm. Limit of quantification is 0.1 µU recombinant Purine Nucleoside Phosphorylase.
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Notes
Purine Nucleoside Phosphorylase (PNP, E.C. 2.4.2.1.) is an enzyme involved in purine metabolism and it catalyzes the cleavage of the glycosidic bond of ribo- or deoxyribonucleosides, in the presence of inorganic phosphate as a second substrate, to generate the purine base and ribose-1-phosphate or deoxyribose-1-phosphate. It is one of the enzymes of the nucleotide salvage pathways that allow the cell to produce nucleotide monophosphates when the de novo synthesis pathway has been interrupted or is non-existent (as is the case in the brain). PNP is a cytosolic enzyme. PNP deficiency disease leads to toxic buildup of deoxyguanosine in T-cells leading to T-lymphocytopenia with no apparent effects on B-lymphocyte function. Inhibition of PNP is an important target for chemotherapeutic applications and treatment of T-cell mediated autoimmune diseases. PNP deficiency is also associated with neurological problems.
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It is the responsibility of our customers to check the necessity of application of REACH Authorisation, and any other relevant authorisations, for their intended uses. -
Platform
Microplate reader
Properties
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Storage instructions
Store at -20°C. Please refer to protocols. -
Components 100 tests Developer 1 vial Hypoxanthine Standard (10 mM) 1 x 100µl Inosine Substrate 1 x 200µl PNP Assay Buffer (10x) 1 x 10ml PNP Positive Control 1 vial U.V. transparent plate (96-well) 1 unit -
Research areas
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Involvement in disease
Defects in PNP are the cause of purine nucleoside phosphorylase deficiency (PNP deficiency) [MIM:613179]. It leads to a severe T-cell immunodeficiency with neurologic disorder in children. -
Sequence similarities
Belongs to the PNP/MTAP phosphorylase family. -
Cellular localization
Cytoplasm > cytoskeleton. - Information by UniProt
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Alternative names
- FLJ94043
- FLJ97288
- FLJ97312
see all
Images
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Typical Hypoxanthine Standard Curve using Purine Nucleoside Phosphorylase Activity Assay Kit (Colorimetric) (ab204707).
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Purine Nucleoside Phosphorylase Activity in Jurkat cell (T-lymphocyte) lysate (3 µg), rat brain lysate (19 µg), and Positive Control.
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PNP specific activity in Jurkat cell lysate and rat brain lysate.