Gene: Fgfr3
Official Full Name: fibroblast growth factor receptor 3provided by MGI
Gene Summary: This gene encodes a member of the fibroblast growth factor receptor family. Members of this family are highly conserved proteins that differ from one another in their ligand affinities and tissue distribution. A representative protein consists of an extracellular region composed of three immunoglobulin-like domains, a single hydrophobic membrane-spanning segment, and a cytoplasmic tyrosine kinase domain. The extracellular portion of the protein interacts with fibroblast growth factors, setting in motion a cascade of downstream signals, ultimately influencing mitogenesis and differentiation. This family member binds acidic and basic fibroblast growth hormone and plays a role in bone development and maintenance. Mutations in this gene may be associated with craniosynostosis and multiple types of skeletal dysplasia. A pseudogene of this gene is located on chromosome 1. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Apr 2011]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO10784 | FGFR3 Knockout cell line (HeLa) | Human | FGFR3 | 1:3~1:6 | Negative | Online Inquiry |
KO10785 | FGFR3 Knockout cell line (HCT 116) | Human | FGFR3 | 1:2~1:4 | Negative | Online Inquiry |
KO10786 | FGFR3 Knockout cell line (HEK293) | Human | FGFR3 | 1:3~1:6 | Negative | Online Inquiry |
KO10787 | FGFR3 Knockout cell line (A549) | Human | FGFR3 | 1:3~1:4 | Negative | Online Inquiry |
Fgfr3 Gene Knockout Cell Lines are genetically engineered cell lines in which the Fibroblast Growth Factor Receptor 3 (FGFR3) gene has been disrupted or deleted. FGFR3 is a key player in various signaling pathways involved in skeletal development, cell proliferation, and differentiation. These knockout cell lines allow researchers to explore the functional role of FGFR3 in vitro, providing a powerful tool for studying associated pathological conditions such as achondroplasia, bladder cancer, and other types of malignancies influenced by aberrant FGFR signaling.
At the molecular level, the Fgfr3 gene plays a crucial role in regulating chondrocyte proliferation and differentiation, impacting overall bone growth and maturation. By utilizing these knockout cell lines, scientists can dissect the intracellular signaling cascades that are disturbed in various diseases, paving the way for novel therapeutic interventions. In particular, they can assess how FGFR3 absence affects cellular behavior, gene expression profiles, and downstream signaling pathways, thereby providing critical insights into the disease mechanisms.
In research and clinical applications, Fgfr3 Gene Knockout Cell Lines enable in-depth studies that can lead to targeted drug development and personalized medicine approaches. By providing a robust system for understanding the implications of FGFR3 loss-of-function mutations, these cell lines hold significant potential in advancing preclinical studies and facilitating translational research.
Compared to traditional models, such as wild-type cell lines or animal models, our Fgfr3 Gene Knockout Cell Lines offer increased specificity and control, allowing researchers to fine-tune experimental conditions and achieve reproducible results. This specificity translates into more accurate assessments of gene function and pathway interactions, enhancing the reliability of research findings.
For researchers and clinicians focused on understanding the complexities of cell signaling and its implications in diseases, our Fgfr3 Gene Knockout Cell Lines represent a vital resource. With the backing of our extensive expertise in genetic engineering and commitment to quality, we deliver products that meet rigorous scientific standards, empowering the scientific community to make significant strides in understanding and treating fibrotic diseases and related disorders.
Please note that all services are for research use only. Not intended for any clinical use.
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