Anti-PNP Antibody (CAB19885)[KO Validated]
- SKU:
- CAB19885
- Product type:
- Antibody
- Reactivity:
- Human
- Mouse
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Cell Biology
Description
Antibody Name: | Anti-PNP Antibody [KO Validated] |
Antibody SKU: | CAB19885 |
Antibody Size: | 20uL, 50uL, 100uL |
Application: | WB IF |
Reactivity: | Human, Mouse |
Host Species: | Rabbit |
Immunogen: | Recombinant protein of human PNP. |
Application: | WB IF |
Recommended Dilution: | WB 1:500 - 1:2000 IF 1:50 - 1:200 |
Reactivity: | Human, Mouse |
Positive Samples: | 293T |
Immunogen: | Recombinant protein of human PNP. |
Purification Method: | Affinity purification |
Storage Buffer: | Store at -20°C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
Isotype: | IgG |
Sequence: | Email for sequence |
Gene ID: | 4860 |
Uniprot: | P00491 |
Cellular Location: | Cytoplasm, cytoskeleton |
Calculated MW: | 32kDa |
Observed MW: | 30KDa |
Synonyms: | PNP, NP, PRO1837, PUNP |
Background: | This gene encodes an enzyme which reversibly catalyzes the phosphorolysis of purine nucleosides. The enzyme is trimeric, containing three identical subunits. Mutations which result in nucleoside phosphorylase deficiency result in defective T-cell (cell-mediated) immunity but can also affect B-cell immunity and antibody responses. Neurologic disorders may also be apparent in patients with immune defects. A known polymorphism at aa position 51 that does not affect enzyme activity has been described. A pseudogene has been identified on chromosome 2. |
UniProt Protein Function: | NP: a metabolic enzyme with purine-nucleoside phosphorylase activity. Defects are the cause of nucleoside phosphorylase deficiency (NP deficiency), with severe T-cell immunodeficiency with neurologic disorder in children. |
UniProt Protein Details: | Protein type:Cofactor and Vitamin Metabolism - nicotinate and nicotinamide; Transferase; EC 2.4.2.1; Nucleotide Metabolism - purine; Nucleotide Metabolism - pyrimidine Chromosomal Location of Human Ortholog: 14q13.1 Cellular Component: cytoplasm; cytosol; intracellular Molecular Function:drug binding; nucleoside binding; phosphate binding; purine binding; purine-nucleoside phosphorylase activity Biological Process: immune response; inosine catabolic process; nicotinamide riboside catabolic process; nucleobase, nucleoside, nucleotide and nucleic acid metabolic process; positive regulation of alpha-beta T cell differentiation; positive regulation of T cell proliferation; purine nucleotide catabolic process; purine salvage; response to drug Disease: Purine Nucleoside Phosphorylase Deficiency |
NCBI Summary: | This gene encodes an enzyme which reversibly catalyzes the phosphorolysis of purine nucleosides. The enzyme is trimeric, containing three identical subunits. Mutations which result in nucleoside phosphorylase deficiency result in defective T-cell (cell-mediated) immunity but can also affect B-cell immunity and antibody responses. Neurologic disorders may also be apparent in patients with immune defects. A known polymorphism at aa position 51 that does not affect enzyme activity has been described. A pseudogene has been identified on chromosome 2. [provided by RefSeq, Jul 2008] |
UniProt Code: | P00491 |
NCBI GenInfo Identifier: | 108935929 |
NCBI Gene ID: | 4860 |
NCBI Accession: | P00491.2 |
UniProt Secondary Accession: | P00491,Q15160, Q5PZ03, B2R8S5, D3DS00, |
UniProt Related Accession: | P00491 |
Molecular Weight: | 32,118 Da |
NCBI Full Name: | Purine nucleoside phosphorylase |
NCBI Synonym Full Names: | purine nucleoside phosphorylase |
NCBI Official Symbol: | PNP |
NCBI Official Synonym Symbols: | NP; PUNP; PRO1837 |
NCBI Protein Information: | purine nucleoside phosphorylase |
UniProt Protein Name: | Purine nucleoside phosphorylase |
UniProt Synonym Protein Names: | Inosine phosphorylase; Inosine-guanosine phosphorylase |
Protein Family: | Polyribonucleotide nucleotidyltransferase |
UniProt Gene Name: | PNP |
UniProt Entry Name: | PNPH_HUMAN |