Gene: TNFAIP3
Official Full Name: TNF alpha induced protein 3provided by HGNC
Gene Summary: This gene was identified as a gene whose expression is rapidly induced by the tumor necrosis factor (TNF). The protein encoded by this gene is a zinc finger protein and ubiqitin-editing enzyme, and has been shown to inhibit NF-kappa B activation as well as TNF-mediated apoptosis. The encoded protein, which has both ubiquitin ligase and deubiquitinase activities, is involved in the cytokine-mediated immune and inflammatory responses. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2012]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
GP00382 | TNFAIP3 gRNA1-gRNA2 KO plasmid | TNFAIP3 | $850 | |||
KO00138 | TNFAIP3 Knockout cell line (A549) | Human | TNFAIP3 | 1:3~1:4 | Negative | Online Inquiry |
KO00139 | TNFAIP3 Knockout cell line (Hep G2) | Human | TNFAIP3 | 1:2~1:4 | Negative | Online Inquiry |
KO00374 | TNFAIP3 Knockout cell line (HeLa) | Human | TNFAIP3 | 1:3~1:6 | Negative | Online Inquiry |
KO10973 | TNFAIP3 Knockout cell line (HCT 116) | Human | TNFAIP3 | 1:2~1:4 | Negative | Online Inquiry |
KO10974 | TNFAIP3 Knockout cell line (HEK293) | Human | TNFAIP3 | 1:3~1:6 | Negative | Online Inquiry |
TNFAIP3 Gene Knockout Cell Lines represent a significant advancement in cellular biology tools, specifically designed to study the role of the TNFAIP3 gene (also known as A20) in diverse biological processes. These cell lines are genetically engineered to disrupt TNFAIP3 expression, allowing researchers to investigate the consequences of A20 deficiency on cellular signaling pathways, inflammation, and immune responses. By knocking out the TNFAIP3 gene, scientists can elucidate its critical functions in maintaining cellular homeostasis and preventing hyperactivation of NF-kB signaling, which is pivotal in various pathological conditions.
The mechanism of action of these knockout cell lines revolves around their ability to mimic disease states in vitro. By providing a controlled environment where TNFAIP3 is absent, researchers can explore aberrant signaling involved in autoimmune diseases, cancer, and infection responses. The TNFAIP3 gene encodes a deubiquitinating enzyme that regulates ubiquitin-mediated signaling, thereby influencing processes like apoptosis and autoimmunity. This makes these cell lines indispensable for studying diseases where TNFAIP3 dysregulation is implicated.
In terms of scientific importance, the TNFAIP3 Gene Knockout Cell Lines offer unparalleled opportunities for investigation in both research and clinical settings. They can be utilized to screen for therapeutic compounds, investigate the interactions of other signaling pathways, and assess the efficacy of potential drug targets. Moreover, these cell lines serve as vital tools for understanding the mechanisms underlying immune responses and inflammatory disorders.
What sets our TNFAIP3 Gene Knockout Cell Lines apart from other genetic models is their high specificity and reliability. Developed from rigorous gene-editing techniques, such as CRISPR-Cas9, these cell lines show consistent knockout efficiency and reproducibility across experiments. The ease of use and ability to be cultured under standard laboratory conditions further enhance their appeal to researchers, facilitating straightforward experimental designs.
In a landscape where precision and accuracy are paramount, the TNFAIP3 Gene Knockout Cell Lines deliver unmatched value to researchers and clinicians aiming to decode complex biological interactions and develop effective therapeutic strategies. Our company brings a wealth of expertise in genetically engineered cell lines, ensuring that our products meet the highest standards of quality and reliability. By choosing our TNFAIP3 knockout products, users are equipped with state-of-the-art resources to advance their biomedical research initiatives.
Please note that all services are for research use only. Not intended for any clinical use.
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