Gene: FBN3
Official Full Name: fibrillin 3provided by HGNC
Gene Summary: This gene encodes a memebr of the fibrillin protein family. Fibrillins are extracellular matrix molecules that assemble into microfibrils in many connective tissues. This gene is most highly expressed in fetal tissues and its protein product is localized to extracellular microfibrils of developing skeletal elements, skin, lung, kidney, and skeletal muscle. This gene is potentially involved in Weill-Marchesani syndrome. [provided by RefSeq, Mar 2016]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO24850 | FBN3 Knockout cell line (HCT 116) | Human | FBN3 | 1:2~1:4 | Negative | Online Inquiry |
FBN3 Gene Knockout Cell Lines represent a cutting-edge biological tool designed for in-depth research on the functional implications of the FBN3 gene, which encodes for fibrillin-3—a critical component of the extracellular matrix and essential for proper skeletal development and elastic fiber formation. By using targeted gene editing technologies such as CRISPR/Cas9, these cell lines exhibit a complete loss of FBN3 expression, providing researchers with a valuable model to investigate the downstream effects of FBN3 deficiency on cellular behavior, signaling pathways, and tissue architecture.
The primary mechanism by which these knockout cell lines operate is through the disruption of the FBN3 gene, leading to altered protein expression patterns. This is instrumental in elucidating the role of FBN3 in various biological processes, including growth regulation, cell differentiation, and the overall structural integrity of connective tissues. By employing these cell lines, researchers can simulate pathological conditions associated with FBN3 mutations, such as skeletal dysplasias, and can explore new therapeutic interventions or drug discoveries aimed at correcting or compensating for these deficiencies.
From a scientific standpoint, FBN3 Gene Knockout Cell Lines hold significant importance in both basic and applied research contexts. They can be utilized for studies in developmental biology, regenerative medicine, and genetic disorders. In clinical settings, these lines can serve as platforms for testing the efficacy of pharmacological agents or gene therapies aimed at restoring functionality in FBN3-related conditions.
Compared to traditional models, such as wild-type cell lines or animal models, FBN3 Gene Knockout Cell Lines offer superior specificity and reproducibility in experimentation, enabling more precise insights into gene function. Their ready availability allows for a rapid turnaround in research timelines, supporting high-throughput screening efforts.
In summary, FBN3 Gene Knockout Cell Lines provide researchers and clinicians with a robust tool to further understand the complexities surrounding fibrillin-related biology. Backed by our commitment to quality and innovation, our company specializes in creating biologically relevant models that accelerate discoveries and enhance the capabilities of researchers worldwide.
Please note that all services are for research use only. Not intended for any clinical use.
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