Gene: TBX19
Official Full Name: T-box transcription factor 19provided by HGNC
Gene Summary: This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. Mutations in this gene were found in patients with isolated deficiency of pituitary POMC-derived ACTH, suggesting an essential role for this gene in differentiation of the pituitary POMC lineage. ACTH deficiency is characterized by adrenal insufficiency symptoms such as weight loss, lack of appetite (anorexia), weakness, nausea, vomiting, and low blood pressure. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO33583 | TBX19 Knockout cell line (HeLa) | Human | TBX19 | 1:3~1:6 | Negative | Online Inquiry |
KO33584 | TBX19 Knockout cell line (HCT 116) | Human | TBX19 | 1:2~1:4 | Negative | Online Inquiry |
KO33585 | TBX19 Knockout cell line (HEK293) | Human | TBX19 | 1:3~1:6 | Negative | Online Inquiry |
TBX19 Gene Knockout Cell Lines are genetically modified cell lines specifically designed to study the function of the TBX19 gene, which encodes T-box transcription factor 19. This transcription factor plays a critical role in endocrine development, particularly in the regulation of pituitary function and the pathophysiology of conditions such as congenital adrenal hyperplasia. By employing CRISPR/Cas9 genome editing technology, these cell lines enable researchers to create a loss-of-function model, allowing for the examination of the downstream effects of TBX19 depletion on other genes and cellular pathways.
The primary functionality of TBX19 Gene Knockout Cell Lines lies in their ability to mimic the physiological conditions present in specific diseases or developmental stages. Researchers can utilize these cell lines to elucidate the molecular mechanisms underlying endocrine disorders, evaluate potential drug targets, and assess cellular responses to therapeutic interventions. Furthermore, these models aid in the identification of gene regulatory networks involving TBX19, thereby advancing our understanding of endocrine signaling pathways.
Scientifically, the application of TBX19 knockout models is pivotal in both research and clinical settings. Researchers can leverage these models to conduct high-throughput screening of compounds that modulate TBX19 activity, potentially leading to novel therapeutic strategies. Clinical relevance is particularly significant as altered TBX19 expression is implicated in various disorders, necessitating effective models for investigating their etiology.
Compared to other gene knockout systems, TBX19 Gene Knockout Cell Lines offer a unique, streamlined approach that boasts enhanced specificity and efficiency. The use of CRISPR technology ensures precise modifications with minimal off-target effects. Additionally, these cell lines are available with extensive characterizations, providing researchers with reliable data on gene expression and functional analyses that serve to expedite experimental timelines.
For researchers and clinicians aiming to delve deeper into the complexities of endocrine regulation and related disorders, TBX19 Gene Knockout Cell Lines present an invaluable resource. Their robust functionality coupled with a clear focus on TBX19-related pathways makes them critical assets for any laboratory committed to advancing knowledge and treatment modalities in endocrinology. Our company specializes in high-quality biological products, and we are dedicated to supporting the scientific community with innovative solutions that enhance research outcomes.
Please note that all services are for research use only. Not intended for any clinical use.
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