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PAX9 Knockout Cell Lines

Gene: PAX9

Official Full Name: paired box 9provided by HGNC

Gene Summary: This gene is a member of the paired box (PAX) family of transcription factors. Members of this gene family typically contain a paired box domain, an octapeptide, and a paired-type homeodomain. These genes play critical roles during fetal development and cancer growth. Mice lacking this gene exhibit impaired development of organs, musculature and the skeleton, including absent and abnormally developed teeth, and neonatal lethality. Mutations in the human gene are associated with selective tooth agenesis-3. [provided by RefSeq, Sep 2015]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO36216 PAX9 Knockout cell line (HeLa) Human PAX9 1:3~1:6 Negative Online Inquiry
KO36217 PAX9 Knockout cell line (HCT 116) Human PAX9 1:2~1:4 Negative Online Inquiry
KO36218 PAX9 Knockout cell line (HEK293) Human PAX9 1:3~1:6 Negative Online Inquiry
KO36219 PAX9 Knockout cell line (A549) Human PAX9 1:3~1:4 Negative Online Inquiry

Background

PAX9 Gene Knockout Cell Lines are specialized cellular models developed to facilitate the study of the PAX9 gene's role in development and disease. The PAX9 gene encodes a transcription factor that is crucial for the proper formation of teeth, bones, and other structures during embryonic development. These knockout cell lines have been meticulously engineered using CRISPR/Cas9 technology to disrupt the PAX9 gene, allowing researchers to investigate the functional consequences of its absence at both cellular and molecular levels.

The primary function of these cell lines is to examine the downstream effects of PAX9 disruption on cellular pathways that govern differentiation, proliferation, and apoptosis. The lack of PAX9 in these cells replicates in vivo conditions, enabling the elucidation of signaling mechanisms impacted by this transcription factor. Researchers can utilize these models to understand pathological conditions like congenital disorders and various cancers associated with PAX9 mutations.

In research and clinical applications, the PAX9 Gene Knockout Cell Lines are a valuable tool for drug discovery and biomarker identification, paving the way for developing novel therapeutic strategies. Given the specificity of the knockout model, scientists can conduct high-throughput screening for pharmacologically active compounds that could restore normal cellular function, offering a significant advantage over traditional models that may mask targeted effects.

What sets our PAX9 Gene Knockout Cell Lines apart from alternatives is their precision and reliability. Each cell line is validated for consistent genetic modification and phenotypic characterization, ensuring reproducibility in experimental conditions. Additionally, they are provided with comprehensive technical support and user-friendly manuals, streamlining their integration into existing workflows.

For researchers and clinicians seeking to unravel the complexities of gene function and its implications in health, the PAX9 Gene Knockout Cell Lines represent an indispensable asset. With our commitment to excellence in biological product development and thorough understanding of genetic engineering techniques, our company stands ready to support your research endeavors with high-quality, innovative solutions.

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

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