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NKX2-1 Knockout Cell Lines

Gene: NKX2-1

Official Full Name: NK2 homeobox 1provided by HGNC

Gene Summary: This gene encodes a protein initially identified as a thyroid-specific transcription factor. The encoded protein binds to the thyroglobulin promoter and regulates the expression of thyroid-specific genes but has also been shown to regulate the expression of genes involved in morphogenesis. Mutations and deletions in this gene are associated with benign hereditary chorea, choreoathetosis, congenital hypothyroidism, and neonatal respiratory distress, and may be associated with thyroid cancer. Multiple transcript variants encoding different isoforms have been found for this gene. This gene shares the symbol/alias 'TTF1' with another gene, transcription termination factor 1, which plays a role in ribosomal gene transcription. [provided by RefSeq, Feb 2014]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO06408 NKX2-1 Knockout cell line (HEK293) Human NKX2-1 1:3~1:6 Negative Online Inquiry

Background

NKX2-1 Gene Knockout Cell Lines represent a cutting-edge tool in molecular biology that allows researchers to study the functions and regulatory mechanisms of the NKX2-1 gene, a critical transcription factor involved in various developmental processes and lung maturation. These cell lines are engineered to specifically disrupt the NKX2-1 gene, facilitating the examination of its role in physiological and pathological conditions, including lung diseases, thyroid function, and neurogenesis.

The mechanism of action behind these knockout cell lines involves CRISPR-Cas9 technology, enabling precise genomic editing that effectively silences NKX2-1 expression. This targeted approach provides a highly reproducible model system for elucidating the gene's contributions to cellular functions and signaling pathways. By utilizing these cell lines, researchers can dissect the impact of NKX2-1 loss-of-function on cellular behavior, aiding in the understanding of complex diseases linked to its dysregulation.

The scientific importance of NKX2-1 Gene Knockout Cell Lines lies in their wide-ranging applications in both basic research and clinical investigations. These models are invaluable for studying the pathophysiology of respiratory and thyroid disorders, as well as potential therapeutic approaches targeting NKX2-1-related pathways. The ability to generate consistent, reproducible results positions these cell lines as a preferred choice for researchers focusing on gene function and cancer biology.

Compared to conventional knockout models, NKX2-1 Gene Knockout Cell Lines offer several advantages. They reduce the time and cost associated with generating and validating transgenic mice models, provide more straightforward experimental setups, and enable high-throughput screening capabilities. These unique selling points make them highly desirable for researchers and clinicians looking to advance their understanding of gene function in a user-friendly format.

Furthermore, the value of NKX2-1 Gene Knockout Cell Lines extends beyond mere experimentation. By offering insights into crucial biological processes, these cell lines can pave the way for new diagnostic, prognostic, and therapeutic strategies within the biomedical field.

At [Your Company Name], we pride ourselves on our expertise in genetic editing technologies and our commitment to supporting the research community. Our extensive portfolio of biological products is designed to facilitate innovative research while upholding the highest standards of quality and reliability.

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

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