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TNFRSF11A Knockout Cell Lines

Gene: TNFRSF11A

Official Full Name: TNF receptor superfamily member 11aprovided by HGNC

Gene Summary: The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptors can interact with various TRAF family proteins, through which this receptor induces the activation of NF-kappa B and MAPK8/JNK. This receptor and its ligand are important regulators of the interaction between T cells and dendritic cells. This receptor is also an essential mediator for osteoclast and lymph node development. Mutations at this locus have been associated with familial expansile osteolysis, autosomal recessive osteopetrosis, and Paget disease of bone. Alternatively spliced transcript variants have been described for this locus. [provided by RefSeq, Aug 2012]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO02904 TNFRSF11A Knockout cell line (HeLa) Human TNFRSF11A 1:3~1:6 Negative Online Inquiry
KO02905 TNFRSF11A Knockout cell line (HCT 116) Human TNFRSF11A 1:2~1:4 Negative Online Inquiry
KO02906 TNFRSF11A Knockout cell line (HEK293) Human TNFRSF11A 1:3~1:6 Negative Online Inquiry
KO02907 TNFRSF11A Knockout cell line (A549) Human TNFRSF11A 1:3~1:4 Negative Online Inquiry

Background

TNFRSF11A Gene Knockout Cell Lines are an advanced tool in molecular biology, specifically designed to facilitate the study of the receptor activator of nuclear factor kappa-Β ligand (RANKL) signaling pathway. This product consists of genetically modified cell lines in which the TNFRSF11A gene, encoding the receptor for RANKL, has been precisely knocked out through CRISPR-Cas9 technology. By eliminating this gene, researchers can investigate the biological functions of RANKL in osteoclastogenesis, immune regulation, and bone metabolism without the confounding influence of TNFRSF11A.

The key function of these knockout cell lines lies in their ability to provide a controlled environment for studying the downstream effects of RANKL signaling on various cellular processes. The absence of TNFRSF11A allows for the examination of altered cellular responses, including changes in gene expression, apoptosis, and cell differentiation. This makes the TNFRSF11A Gene Knockout Cell Lines invaluable for dissecting complex pathways and identifying potential therapeutic targets for diseases such as osteoporosis, rheumatoid arthritis, and bone-related malignancies.

Scientifically, the implications of utilizing these cell lines extend to both research and clinical applications. For researchers studying osteoclast differentiation or immune system interactions, these cell lines facilitate innovative approaches to understanding pathophysiological conditions. In clinical settings, findings derived from experiments using these knockout lines could lead to the development of novel treatments aimed at modulating RANKL signaling in bone diseases, thus translating basic research into practical healthcare solutions.

What sets TNFRSF11A Gene Knockout Cell Lines apart from other genetic toolkits is their specificity and efficacy. Unlike traditional methods which may involve non-specific knockdowns or overexpression approaches, the precision of CRISPR-Cas9 technology ensures an accurate deletion of the target gene, thereby providing robust and reproducible results. Furthermore, these cell lines are rigorously validated to confirm loss of function, offering high reliability for experimental outcomes.

For researchers and clinicians invested in advancing our understanding of skeletal biology and related pathologies, the TNFRSF11A Gene Knockout Cell Lines represent an indispensable resource. Leveraging cutting-edge genetic modification techniques, these cell lines embody a commitment to supporting scientific inquiry in a rapidly evolving field. Our company specializes in providing high-quality biological products, backed by extensive expertise in genetic engineering and molecular biology, ensuring that our customers have access to tools that drive innovation and discovery in their research endeavors.

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

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