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TBL1XR1 Knockout Cell Lines

Gene: TBL1XR1

Official Full Name: TBL1X/Y related 1provided by HGNC

Gene Summary: This gene is a member of the WD40 repeat-containing gene family and shares sequence similarity with transducin (beta)-like 1X-linked (TBL1X). The protein encoded by this gene is thought to be a component of both nuclear receptor corepressor (N-CoR) and histone deacetylase 3 (HDAC 3) complexes, and is required for transcriptional activation by a variety of transcription factors. Mutations in these gene have been associated with some autism spectrum disorders, and one finding suggests that haploinsufficiency of this gene may be a cause of intellectual disability with dysmorphism. Mutations in this gene as well as recurrent translocations involving this gene have also been observed in some tumors. [provided by RefSeq, Mar 2016]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO11664 TBL1XR1 Knockout cell line (HeLa) Human TBL1XR1 1:3~1:6 Negative Online Inquiry
KO11665 TBL1XR1 Knockout cell line (HCT 116) Human TBL1XR1 1:2~1:4 Negative Online Inquiry
KO11666 TBL1XR1 Knockout cell line (HEK293) Human TBL1XR1 1:3~1:6 Negative Online Inquiry
KO11667 TBL1XR1 Knockout cell line (A549) Human TBL1XR1 1:3~1:4 Negative Online Inquiry

Background

TBL1XR1 Gene Knockout Cell Lines are advanced cellular models specifically engineered to lack the TBL1XR1 gene, which plays a critical role in the regulation of multiple signaling pathways, including Wnt and Notch. These knockout cell lines serve as powerful tools for investigating the biological roles of TBL1XR1, especially in contexts such as cancer research, developmental biology, and cellular differentiation. By disrupting the expression of this gene, researchers can elucidate its contributions to cellular processes such as proliferation, apoptosis, and gene expression modulation.

The keystone mechanisms by which TBL1XR1 exerts its influence on cellular behavior involve its interaction with various transcription factors and components of the signaling pathways mentioned earlier. In particular, its role as a co-activator enables the transcriptional activation of target genes involved in cell fate determination and oncogenesis. Utilizing TBL1XR1 knockout cell lines allows researchers to observe phenotypic alterations that occur when this regulatory mechanism is disrupted, thus providing insights into potential therapeutic targets.

Scientific importance lies in the versatile applications of these knockout lines in research and clinical settings. By using TBL1XR1 knockout cells, investigators can better understand the underlying mechanisms of diseases in which this gene is implicated, such as specific cancer types or developmental disorders. These insights can lead to innovative therapeutic strategies and improved clinical outcomes.

Compared to traditional cell lines, TBL1XR1 knockout cell lines offer unique advantages, including the specificity of gene targeting and the ability to pair with CRISPR-Cas9 technology for efficient experiments. Their use simplifies the study of gene function in a controlled environment, enabling more precise investigations of cellular behavior without the confounding effects of the TBL1XR1 protein.

The value of TBL1XR1 Gene Knockout Cell Lines extends to researchers, clinicians, and pharmaceutical developers who are striving to advance medical knowledge and treatment options. By providing a deeper understanding of the TBL1XR1 pathway, these cell lines contribute significantly to the development of targeted therapies and the advancement of precision medicine.

Our company has a strong commitment to providing high-quality biological products that enable groundbreaking research. With expertise in gene editing technologies and cellular biology, we ensure that our products meet the highest standards of reliability and performance, empowering scientists to achieve their research objectives effectively.

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

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