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PNP Knockout Cell Lines

Gene: PNP

Official Full Name: purine nucleoside phosphorylaseprovided by HGNC

Gene 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]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO06389 PNP Knockout cell line (HeLa) Human PNP 1:3~1:6 Negative Online Inquiry
KO06390 PNP Knockout cell line (HCT 116) Human PNP 1:2~1:4 Negative Online Inquiry
KO06391 PNP Knockout cell line (HEK293) Human PNP 1:3~1:6 Negative Online Inquiry
KO06392 PNP Knockout cell line (A549) Human PNP 1:3~1:4 Negative Online Inquiry

Background

PNP Gene Knockout Cell Lines are specially engineered cell lines wherein the purine nucleoside phosphorylase (PNP) gene has been inactivated or knocked out, allowing researchers to investigate the functional roles of PNP in various biological processes. PNP is an essential enzyme involved in purine metabolism, particularly in the salvage pathway that recycles purines from nucleic acids. By disrupting the PNP gene, these cell lines serve as a powerful tool for studying metabolic pathways, cellular responses to stress, and the mechanisms underlying certain genetic disorders, including immunodeficiencies.

The key function of PNP knockout cell lines lies in their ability to model the metabolic consequences associated with PNP deficiency. These cell lines enable scientists to delve deeper into purine metabolic dysfunctions that may lead to elevated levels of toxic metabolites, ultimately impacting cellular growth and function. Mechanistically, researchers can utilize these models to better understand the adaptive responses of cells to purine depletion and explore therapeutic targets for metabolic diseases.

Scientifically, PNP gene knockout cell lines are invaluable in both basic and applied research contexts. They are crucial in the study of gene therapy approaches for PNP-deficient conditions and provide insights into potential drug development strategies. Furthermore, these cell lines are instrumental in testing and validating novel therapeutic compounds aimed at manipulating purine metabolism to enhance efficacy in treating various diseases.

Compared to alternative gene knockout models, PNP knockout cell lines offer the unique advantage of relevance to specific clinical conditions associated with purine metabolism. Their relative ease of use, along with robust reproducibility, makes them an appealing choice for research labs seeking reliable models to study complex biological phenomena.

For researchers and clinicians, investing in PNP Gene Knockout Cell Lines translates to access to a top-tier resource that enables groundbreaking discoveries in metabolic biology and novel therapeutic interventions. Our company specializes in precise genetic modifications, ensuring that our cell lines maintain strict quality control and are optimized for various research applications. By choosing our PNP Gene Knockout Cell Lines, you are leveraging our expertise and commitment to advancing scientific knowledge and innovation in the life sciences.

Please note that all services are for research use only. Not intended for any clinical use.

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