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TRAF3 Knockout Cell Lines

Gene: TRAF3

Official Full Name: TNF receptor associated factor 3provided by HGNC

Gene Summary: The protein encoded by this gene is a member of the TNF receptor associated factor (TRAF) protein family. TRAF proteins associate with, and mediate the signal transduction from, members of the TNF receptor (TNFR) superfamily. This protein participates in the signal transduction of CD40, a TNFR family member important for the activation of the immune response. This protein is found to be a critical component of the lymphotoxin-beta receptor (LTbetaR) signaling complex, which induces NF-kappaB activation and cell death initiated by LTbeta ligation. Epstein-Barr virus encoded latent infection membrane protein-1 (LMP1) can interact with this and several other members of the TRAF family, which may be essential for the oncogenic effects of LMP1. The protein also plays a role in the regulation of antiviral response. Mutations in this are associated with Encephalopathy, acute, infection-induced, herpes-specific 5. [provided by RefSeq, Jul 2020]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO10956 TRAF3 Knockout cell line (HeLa) Human TRAF3 1:3~1:6 Negative Online Inquiry
KO10957 TRAF3 Knockout cell line (HCT 116) Human TRAF3 1:2~1:4 Negative Online Inquiry
KO10958 TRAF3 Knockout cell line (HEK293) Human TRAF3 1:3~1:6 Negative Online Inquiry
KO10959 TRAF3 Knockout cell line (A549) Human TRAF3 1:3~1:4 Negative Online Inquiry

Background

TRAF3 Gene Knockout Cell Lines are genetically engineered cellular models that have had the TRAF3 gene, which plays a critical role in immune signaling pathways, selectively deleted. By creating these knockout lines, researchers can investigate the specific functions of TRAF3 in various biological processes, particularly those related to immune response, inflammation, and cellular signaling.

The primary function of TRAF3 involves mediating downstream signaling pathways for several receptors, including members of the TNF receptor superfamily and the Toll-like receptor family. When TRAF3 is absent, it affects the activation of NF-kB and IRF pathways, ultimately influencing the production of pro-inflammatory cytokines and B cell survival. This mechanism allows the TRAF3 knockout cell lines to serve as valuable tools for understanding how TRAF3 contributes to immune system dysregulation and the development of autoimmune diseases, making them particularly relevant in preclinical drug testing and therapeutic development.

In research and clinical applications, these cell lines are indispensable for elucidating the underlying mechanisms of immune-related conditions and evaluating potential treatments that target TRAF3-associated pathways. Unlike conventional cell lines, the TRAF3 knockout variant provides a more accurate reflection of the physiological states observed in immune cell populations, enabling researchers to derive insights into the roles of this gene in health and disease.

The distinct advantage of using TRAF3 Gene Knockout Cell Lines lies in their specific focus on the manipulation of immune signaling which is often overlooked in other knockout models. This specificity allows for targeted investigations that can lead to novel therapeutic strategies and biomarker development, thereby accelerating the pace of immunological research.

Researchers and clinicians stand to gain from these knockout models, as they offer a focused means to explore TRAF3's contribution to diverse biological processes and diseases. With our extensive expertise in developing cutting-edge biological products, our commitment to high-quality, reliable cell models ensures that you have the tools necessary to advance your research agenda.

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

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