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OAZ2 Knockout Cell Lines

Gene: OAZ2

Official Full Name: ornithine decarboxylase antizyme 2provided by HGNC

Gene Summary: The protein encoded by this gene belongs to the ornithine decarboxylase antizyme family, which plays a role in cell growth and proliferation by regulating intracellular polyamines. Expression of antizymes requires +1 ribosomal frameshifting, which is enhanced by high levels of polyamines. Antizymes in turn bind to and inhibit ornithine decarboxylase (ODC), the key enzyme in polyamine biosynthesis; thus, completing the auto-regulatory circuit. This gene encodes antizyme 2, the second member of the antizyme family. Like antizyme 1, antizyme 2 has broad tissue distribution, inhibits ODC activity and polyamine uptake, and stimulates ODC degradation in vivo; however, it fails to promote ODC degradation in vitro. Antizyme 2 is expressed at lower levels than antizyme 1, but is evolutionary more conserved, suggesting it likely has an important biological role. Studies also show different subcellular localization of antizymes 1 and 2, indicating specific function for each antizyme in discrete compartments of the cell. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2014]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO36279 OAZ2 Knockout cell line (HeLa) Human OAZ2 1:3~1:6 Negative Online Inquiry
KO36280 OAZ2 Knockout cell line (HCT 116) Human OAZ2 1:2~1:4 Negative Online Inquiry
KO36281 OAZ2 Knockout cell line (HEK293) Human OAZ2 1:3~1:6 Negative Online Inquiry
KO36282 OAZ2 Knockout cell line (A549) Human OAZ2 1:3~1:4 Negative Online Inquiry

Background

OAZ2 Gene Knockout Cell Lines are specialized cellular models meticulously engineered to possess a deletion of the OAZ2 gene, which is known to play a crucial role in polyamine metabolism, cell proliferation, and differentiation. By utilizing CRISPR-Cas9 technology, these cell lines provide a robust tool for investigating the biological implications of OAZ2 deficiency and its involvement in various physiological and pathological contexts.

The key mechanisms behind OAZ2 functionality revolve around its regulatory influence on ornithine decarboxylase, the first enzyme in polyamine biosynthesis. The knockout of this gene leads to altered levels of polyamines such as putrescine, spermidine, and spermine, affecting cellular signaling pathways that govern growth and apoptosis. Through these knockout models, researchers can gain deeper insights into how OAZ2 impacts cancer biology, neurodegenerative diseases, and tissue regeneration processes.

The scientific importance of OAZ2 Gene Knockout Cell Lines extends to their applications in both research and clinical settings. They serve as invaluable resources for studying gene function, examining drug responses, and unraveling the molecular mechanisms of diseases linked to polyamine dysregulation. Furthermore, they can facilitate high-throughput screening for therapeutic agents that target polyamine metabolism—offering promising avenues for novel treatment strategies.

Compared to traditional wild-type cell lines, OAZ2 Gene Knockout Cell Lines provide specific advantages, including enhanced fidelity in simulating certain disease states and enabling clearer interpretation of gene function through loss-of-function analysis. This specificity paves the way for more precise scientific inquiries, yielding potentially transformative insights in the field.

Researchers and clinicians can derive significant value from these knockout lines as they equip users with a highly relevant system to dissect complex biological questions and expedite drug discovery processes. The ability to delineate the role of OAZ2 within various biological frameworks strengthens the pursuit of innovative therapeutic interventions.

With a commitment to excellence, our company brings a wealth of expertise in the development of advanced biological products, ensuring that our OAZ2 Gene Knockout Cell Lines meet rigorous scientific standards while providing user-friendly solutions to support cutting-edge research and clinical applications.

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

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