Gene: FSD1
Official Full Name: fibronectin type III and SPRY domain containing 1provided by HGNC
Gene Summary: This gene encodes a centrosome associated protein that is characterized by an N-terminal coiled-coil region downstream of B-box (BBC) domain, a central fibronectin type III domain, and a C-terminal repeats in splA and RyR (SPRY) domain. The encoded protein associates with a subset of microtubules and may be involved in the stability and organization of microtubules during cytokinesis. [provided by RefSeq, Apr 2009]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO17535 | FSD1 Knockout cell line (HeLa) | Human | FSD1 | 1:3~1:6 | Negative | Online Inquiry |
KO17536 | FSD1 Knockout cell line (HCT 116) | Human | FSD1 | 1:2~1:4 | Negative | Online Inquiry |
KO17537 | FSD1 Knockout cell line (HEK293) | Human | FSD1 | 1:3~1:6 | Negative | Online Inquiry |
KO17538 | FSD1 Knockout cell line (A549) | Human | FSD1 | 1:3~1:4 | Negative | Online Inquiry |
FSD1 Gene Knockout Cell Lines are genetically engineered cellular models that have undergone targeted disruption of the FSD1 gene, facilitating the investigation of its role in various biological processes and disease mechanisms. The knockout of FSD1 allows researchers to study the functional contributions of this gene by observing phenotypic changes, cellular behaviors, and biochemical pathways in vitro, providing a powerful tool for elucidating gene function.
The primary mechanism of action involves the CRISPR/Cas9 technology, which enables precise editing of DNA sequences to create the knockout. This technique not only ensures high specificity in gene targeting but also facilitates the assessment of downstream effects on cellular metabolism, signaling pathways, and gene expression profiles. Upon knockout, alterations in cellular responses can be monitored through various assays, effectively linking gene function to phenotypic outcomes.
From a scientific standpoint, FSD1 Gene Knockout Cell Lines hold immense importance in both research and clinical settings. They are pivotal for studying diseases such as cancer, metabolic disorders, and neurodegenerative conditions where FSD1 may play a role. Furthermore, these models are invaluable for drug development processes, as they allow for the assessment of therapeutic interventions in genetically relevant contexts.
Compared to alternative cellular models that rely on overexpression or transient knockdown approaches, FSD1 Gene Knockout Cell Lines offer a stable and reproducible system to provide insights into gene function with far greater accuracy. Their long-term viability ensures consistent results across experiments, reducing variability and enhancing the reliability of findings.
For researchers and clinicians keen on advancing their understanding and treatments of diseases linked to the FSD1 gene, these knockout cell lines are indispensable. They significantly streamline experimental workflows and enrich the data quality, thereby accelerating discoveries in gene function and potential therapeutic avenues.
Our company prides itself on its expertise in the development and production of high-quality biological products. By leveraging cutting-edge gene-editing technologies and extensive scientific knowledge, we ensure that our offerings, such as FSD1 Gene Knockout Cell Lines, meet the rigorous standards required for groundbreaking research and clinical applications.
Please note that all services are for research use only. Not intended for any clinical use.
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