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PITX2 Knockout Cell Lines

Gene: PITX2

Official Full Name: paired like homeodomain 2provided by HGNC

Gene Summary: This gene encodes a member of the RIEG/PITX homeobox family, which is in the bicoid class of homeodomain proteins. The encoded protein acts as a transcription factor and regulates procollagen lysyl hydroxylase gene expression. This protein plays a role in the terminal differentiation of somatotroph and lactotroph cell phenotypes, is involved in the development of the eye, tooth and abdominal organs, and acts as a transcriptional regulator involved in basal and hormone-regulated activity of prolactin. Mutations in this gene are associated with Axenfeld-Rieger syndrome, iridogoniodysgenesis syndrome, and sporadic cases of Peters anomaly. A similar protein in other vertebrates is involved in the determination of left-right asymmetry during development. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO11514 PITX2 Knockout cell line (HeLa) Human PITX2 1:3~1:6 Negative Online Inquiry
KO11515 PITX2 Knockout cell line (HCT 116) Human PITX2 1:2~1:4 Negative Online Inquiry
KO11516 PITX2 Knockout cell line (HEK293) Human PITX2 1:3~1:6 Negative Online Inquiry
KO11517 PITX2 Knockout cell line (A549) Human PITX2 1:3~1:4 Negative Online Inquiry

Background

PITX2 Gene Knockout Cell Lines are genetically engineered cellular models designed to study the functional implications of the PITX2 gene, which plays a critical role in various biological processes, including embryonic development and organogenesis. These cell lines have been created through precise gene editing techniques, such as CRISPR-Cas9, facilitating the complete ablation of PITX2 expression. By eliminating the PITX2 gene, researchers can closely examine its impact on cellular behavior, signaling pathways, and developmental anomalies, providing invaluable insights into its role in health and disease.

The key mechanism behind the functionality of PITX2 Gene Knockout Cell Lines lies in their ability to mimic conditions of PITX2 deficiency. This allows for detailed investigations into disease models, particularly in relation to congenital heart diseases and other disorders associated with dysregulated PITX2 activity. The lack of PITX2 expression in these cell lines makes them an indispensable tool for understanding the gene's role in specific molecular pathways and for screening potential therapeutic interventions.

Scientifically, these cell lines are of paramount importance in both basic research and clinical settings, as they facilitate a deeper understanding of gene function and contribute to the discovery of novel targets for drug development. Considering the growing interest in personalized medicine and gene therapy, PITX2 knockout models are particularly relevant for elucidating the underlying mechanisms of various pathologies.

Compared to alternative models, the PITX2 Gene Knockout Cell Lines offer superior specificity and controlled genetic background, enabling researchers to generate reliable and reproducible results. Their ability to bridge basic research with translational applications makes them an attractive option for laboratories focused on genetics, developmental biology, and regenerative medicine.

For researchers and clinicians seeking to unravel the complexities of gene function and its implications in disease, these cell lines represent a significant investment. They not only enhance experimental precision but also pave the way for innovative therapeutic approaches.

Our company prides itself on a strong foundation in genetic engineering and cell line development, offering high-quality biological products that empower scientific exploration and the advancement of healthcare solutions.

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

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