Gene: FOLR1
Official Full Name: folate receptor alphaprovided by HGNC
Gene Summary: The protein encoded by this gene is a member of the folate receptor family. Members of this gene family bind folic acid and its reduced derivatives, and transport 5-methyltetrahydrofolate into cells. This gene product is a secreted protein that either anchors to membranes via a glycosyl-phosphatidylinositol linkage or exists in a soluble form. Mutations in this gene have been associated with neurodegeneration due to cerebral folate transport deficiency. Due to the presence of two promoters, multiple transcription start sites, and alternative splicing, multiple transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Oct 2009]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO01394 | FOLR1 Knockout cell line (HeLa) | Human | FOLR1 | 1:3~1:6 | Negative | Online Inquiry |
KO09993 | FOLR1 Knockout cell line (HCT 116) | Human | FOLR1 | 1:2~1:4 | Negative | Online Inquiry |
KO09994 | FOLR1 Knockout cell line (HEK293) | Human | FOLR1 | 1:3~1:6 | Negative | Online Inquiry |
FOLR1 Gene Knockout Cell Lines represent a significant advancement in molecular biology research, specifically designed to facilitate the investigation of the folate receptor 1 (FOLR1) gene's role in cellular processes. These genetically engineered cell lines have been developed by utilizing CRISPR-Cas9 technologies, resulting in precise and efficient knockout of the FOLR1 gene. This loss-of-function model allows researchers to explore the biological consequences of FOLR1 deficiency, including its impact on folate metabolism, cell proliferation, and tumor progression, thereby enhancing our understanding of diseases associated with altered folate receptor activity.
The key mechanism of these knockout cell lines revolves around the targeted disruption of the FOLR1 gene, which encodes a receptor critical for folate uptake. By eliminating FOLR1 expression, the cell lines serve as a vital tool for elucidating the receptor's involvement in various pathways, including those associated with cancer biology and developmental processes. Researchers can monitor changes in cell behavior, metabolism, and gene expression, providing comprehensive insight into the functional pathways affected by the absence of FOLR1.
From a scientific perspective, FOLR1 Gene Knockout Cell Lines are invaluable in both research and clinical applications. They offer a unique platform for the study of folate metabolism-related disorders, potentially paving the way for novel therapeutic targets in cancer treatment and pharmacogenomics. Furthermore, these cell lines facilitate the development of targeted therapies that exploit the differential expression of folate receptors in tumor cells, presenting an opportunity to enhance treatment efficacy and reduce systemic toxicity.
One of the unique selling points of FOLR1 Gene Knockout Cell Lines is their high specificity and reproducibility compared to other common gene-editing tools. Unlike traditional knockout models, which can often exhibit variable phenotypic outcomes, these cell lines provide consistent performance across experiments. Additionally, their compatibility with various molecular assays allows for seamless integration into existing research workflows, making them a practical choice for both novice and experienced researchers.
In conclusion, FOLR1 Gene Knockout Cell Lines are a pivotal resource for those delving into the complexities of folate-mediated pathways in health and disease. By providing a robust model for studying the biological implications of FOLR1 loss, these cell lines hold promise for advancing knowledge in the field of cellular biology and oncology. Our company takes pride in its commitment to excellence in genetic engineering, equipping researchers with state-of-the-art tools to drive innovation and discovery in biological research.
Please note that all services are for research use only. Not intended for any clinical use.
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