Purine Nucleoside Phosphorylase Activity Assay Kit (Fluorometric) (ab204706)
Key features and details
- Assay type: Enzyme activity
- Detection method: Fluorescent
- Platform: Microplate reader
- Sample type: Cell Lysate, Purified protein, Tissue Lysate
- Sensitivity: 0.005 µU
Overview
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Product name
Purine Nucleoside Phosphorylase Activity Assay Kit (Fluorometric)
See all Nucleoside phosphorylase kits -
Detection method
Fluorescent -
Sample type
Cell Lysate, Purified protein, Tissue Lysate -
Assay type
Enzyme activity -
Sensitivity
0.005 µU -
Species reactivity
Reacts with: Mammals, Other species -
Product overview
Purine Nucleoside Phosphorylase Activity Assay Kit (Fluorometric) (ab204706) is an assay where hypoxanthine formed from the breakdown of inosine is detected via a multi-step reaction, resulting in the generation of an intermediate that reacts with the PNP Probe. The fluorescent product is measured at Ex/Em = 535/587 nm. Limit of quantification is 0.005 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 allows 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 Enzyme Mix 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 PNP Probe (in dry DMSO) 1 x 200µl -
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