Gene: FOXS1
Official Full Name: forkhead box S1provided by HGNC
Gene Summary: The forkhead family of transcription factors belongs to the winged helix class of DNA-binding proteins. The protein encoded by this intronless gene contains a forkhead domain and is found predominantly in aorta and kidney. The function of the encoded protein is unknown. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO37855 | FOXS1 Knockout cell line (HeLa) | Human | FOXS1 | 1:3~1:6 | Negative | Online Inquiry |
KO37856 | FOXS1 Knockout cell line (A549) | Human | FOXS1 | 1:3~1:4 | Negative | Online Inquiry |
FOXS1 Gene Knockout Cell Lines are highly specialized cellular models designed to investigate the role of the FOXS1 gene in various biological processes, particularly in relation to cell development and differentiation. These knockout cell lines are generated through state-of-the-art gene editing technologies, specifically CRISPR-Cas9, ensuring precise disruption of the FOXS1 gene across different cell types. By knocking out this gene, researchers can identify the phenotype changes and molecular pathways influenced by the loss of FOXS1 expression, thereby elucidating its function in cellular biology and disease mechanisms.
The key mechanism of these cell lines involves the deletion of FOXS1, which typically encodes a forkhead transcription factor playing a critical role in regulating gene expression involved in key developmental processes. Disruption of FOXS1 has been linked to various conditions, including certain cancers and developmental disorders, making these knockout models invaluable in advancing scientific understanding and therapeutic strategies.
Scientifically, the FOXS1 Gene Knockout Cell Lines have significant applications in both research and clinical settings. In laboratories, these models enable researchers to explore FOXS1's contributions to signaling pathways, drug response, and genetic interactions in vitro. Clinically, insights gained can drive the development of targeted therapies aimed at conditions related to FOXS1 dysfunction, thereby aiming to provide more effective treatment options for patients.
What sets these knockout cell lines apart from traditional models is the precision and reliability associated with CRISPR technology, coupled with thoroughly validated performance in functional assays. Additionally, they offer an unparalleled opportunity to replicate human cellular behaviors, thus enhancing the translatability of research findings into clinical applications.
For researchers and clinicians, investing in FOXS1 Gene Knockout Cell Lines opens new avenues for exploration, promising a deeper understanding of genetic influence on disease pathology. Our company is committed to providing top-tier biological research products, backed by extensive expertise in gene editing technologies, ensuring that researchers have access to the tools necessary for advancing their work in genetics and cell biology.
Please note that all services are for research use only. Not intended for any clinical use.
If your question is not addressed through these resources, you can fill out the online form below and we will answer your question as soon as possible.
There is no product in your cart. |
CD Biosynsis is a leading customer-focused biotechnology company dedicated to providing high-quality products, comprehensive service packages, and tailored solutions to support and facilitate the applications of synthetic biology in a wide range of areas.