Gene: THRB
Official Full Name: thyroid hormone receptor betaprovided by HGNC
Gene Summary: The protein encoded by this gene is a nuclear hormone receptor for triiodothyronine. It is one of the several receptors for thyroid hormone, and has been shown to mediate the biological activities of thyroid hormone. Knockout studies in mice suggest that the different receptors, while having certain extent of redundancy, may mediate different functions of thyroid hormone. Mutations in this gene are known to be a cause of generalized thyroid hormone resistance (GTHR), a syndrome characterized by goiter and high levels of circulating thyroid hormone (T3-T4), with normal or slightly elevated thyroid stimulating hormone (TSH). Several alternatively spliced transcript variants encoding the same protein have been observed for this gene. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO05434 | THRB Knockout cell line (HCT 116) | Human | THRB | 1:2~1:4 | Negative | Online Inquiry |
KO05435 | THRB Knockout cell line (HEK293) | Human | THRB | 1:3~1:6 | Negative | Online Inquiry |
KO05436 | THRB Knockout cell line (A549) | Human | THRB | 1:3~1:4 | Negative | Online Inquiry |
THRB Gene Knockout Cell Lines are genetically engineered cellular models that facilitate the study of the thyroid hormone receptor beta (THRB) gene's function. These cell lines are created using advanced CRISPR/Cas9 technology to selectively disrupt THRB, allowing researchers to investigate the physiological and molecular effects of its loss. By generating a specific knockout of the THRB gene, these cell lines provide a versatile and robust platform for elucidating the role of thyroid hormones in various biological processes.
The primary function of these knockout cell lines lies in their ability to mimic pathological conditions where THRB signaling is altered, enabling researchers to explore the downstream effects on metabolic pathways, cell proliferation, differentiation, and gene expression. This is critical for understanding the complexities of diseases associated with thyroid dysfunction, including obesity, cardiovascular diseases, and metabolic syndromes. The knockout model allows for detailed analyses of THRB's role within the endocrine system, potentially revealing therapeutic targets for intervention.
The scientific importance of THRB Gene Knockout Cell Lines extends to both basic and applied research. In clinical settings, these models can help in the development of novel treatments by providing insights into the mechanisms of thyroid hormone action, which can be pivotal in drug discovery and development. Furthermore, these cell lines can support studies aimed at understanding resistance to thyroid hormone therapies, benefiting patient management strategies.
What sets THRB Gene Knockout Cell Lines apart from alternative models is the precision and specificity of the CRISPR/Cas9 technology employed in their creation. Unlike traditional gene editing methods, this approach minimizes off-target effects while enabling a clean and effective knockout. This high level of precision ensures that experiments yield reproducible and reliable results, enhancing the validity of research findings.
For researchers and clinicians, the value of THRB Gene Knockout Cell Lines lies in their ability to accelerate the discovery process and to enable breakthroughs in understanding thyroid-related disorders. By utilizing these cell lines, laboratories can perform high-throughput screening for therapeutic compounds and better characterize the molecular underpinnings of disease states.
Our company is dedicated to providing cutting-edge biological products designed to advance scientific research. With expertise in genetic engineering and a commitment to quality, we ensure that our THRB Gene Knockout Cell Lines meet the highest standards, empowering researchers to achieve new levels of discovery and innovation in their studies.
Please note that all services are for research use only. Not intended for any clinical use.
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