Gene: FOXD1
Official Full Name: forkhead box D1provided by HGNC
Gene Summary: This gene belongs to the forkhead family of transcription factors which are characterized by a distinct forkhead domain. Studies of the orthologous mouse protein indicate that it functions in kidney development by promoting nephron progenitor differentiation, and it also functions in the development of the retina and optic chiasm. It may also regulate inflammatory reactions and prevent autoimmunity. [provided by RefSeq, Apr 2014]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO37864 | FOXD1 Knockout cell line (HeLa) | Human | FOXD1 | 1:3~1:6 | Negative | Online Inquiry |
KO37865 | FOXD1 Knockout cell line (HCT 116) | Human | FOXD1 | 1:2~1:4 | Negative | Online Inquiry |
KO37866 | FOXD1 Knockout cell line (HEK293) | Human | FOXD1 | 1:3~1:6 | Negative | Online Inquiry |
KO37867 | FOXD1 Knockout cell line (A549) | Human | FOXD1 | 1:3~1:4 | Negative | Online Inquiry |
FOXD1 Gene Knockout Cell Lines are genetically modified cell lines designed to specifically eliminate the expression of the FOXD1 gene. This gene encodes a forkhead box transcription factor that plays a critical role in various developmental processes and cellular functions. By utilizing advanced CRISPR-Cas9 gene editing technology, these knockout cell lines allow researchers to study the biological implications of FOXD1 depletion in a controlled environment, providing essential insights into the gene’s role in development, disease mechanisms, and cellular behavior.
The primary function of these cell lines lies in their ability to facilitate the investigation of FOXD1's regulatory pathways and its impact on gene expression. Researchers can observe phenotypic changes, assess cell proliferation, and examine alterations in signaling pathways associated with FOXD1 knockdown. This tool is invaluable for elucidating the role of FOXD1 in cancer biology, stem cell differentiation, and other pathophysiological conditions.
The scientific importance of FOXD1 Gene Knockout Cell Lines extends to numerous applications in both research and clinical settings. They are crucial for conducting functional studies that inform drug development, gene therapy research, and therapeutic interventions aimed at targeting FOXD1-related disorders. Their application can lead to a better understanding of oncogenesis and therapeutic resistance in malignancies, making them an essential resource for preclinical research.
One of the unique selling points of our FOXD1 Gene Knockout Cell Lines is their high efficiency in producing stable and reproducible knockouts when compared to traditional methods. This results in less variability and greater reliability in experimental outcomes, enhancing the accuracy of research findings. Additionally, our cell lines come with comprehensive support and characterization data, enabling researchers to focus on their studies rather than troubleshooting.
By integrating precision gene editing with robust cell culture systems, FOXD1 Gene Knockout Cell Lines represent a significant advancement in genetic research tools. Their value lies in facilitating deep investigations into FOXD1's biological role and therapeutic potential, thereby empowering researchers and clinicians to uncover novel insights and develop innovative treatments. Our company is dedicated to providing cutting-edge biological products and resources, ensuring that our clients are equipped with the tools necessary for groundbreaking research and discovery.
Please note that all services are for research use only. Not intended for any clinical use.
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