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FLNB Knockout Cell Lines

Gene: FLNB

Official Full Name: filamin Bprovided by HGNC

Gene Summary: This gene encodes a member of the filamin family. The encoded protein interacts with glycoprotein Ib alpha as part of the process to repair vascular injuries. The platelet glycoprotein Ib complex includes glycoprotein Ib alpha, and it binds the actin cytoskeleton. Mutations in this gene have been found in several conditions: atelosteogenesis type 1 and type 3; boomerang dysplasia; autosomal dominant Larsen syndrome; and spondylocarpotarsal synostosis syndrome. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Nov 2009]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO10772 FLNB Knockout cell line (HeLa) Human FLNB 1:3~1:6 Negative Online Inquiry
KO10773 FLNB Knockout cell line (HCT 116) Human FLNB 1:2~1:4 Negative Online Inquiry
KO10774 FLNB Knockout cell line (HEK293) Human FLNB 1:3~1:6 Negative Online Inquiry
KO10775 FLNB Knockout cell line (A549) Human FLNB 1:3~1:4 Negative Online Inquiry

Background

FLNB Gene Knockout Cell Lines are specifically engineered cellular models that have had the filamin B (FLNB) gene disrupted or eliminated. Filamin B is a crucial actin-binding protein that plays a key role in maintaining cellular structure and signaling pathways. The creation of FLNB knockout cell lines allows researchers to study the highly complex pathways in which filamin B is involved, facilitating insights into both normal physiological processes and various pathologies, including developmental disorders and certain cancers.

These cell lines function by enabling the analysis of gene function and protein interactions in a controlled environment. Researchers can utilize these knockout models to assess the downstream effects of the absence of FLNB, scrutinize how cellular architecture is impacted, and examine alterations in cell signaling and migration. Such mechanistic studies are pivotal in understanding diseases linked to aberrant cellular behavior.

The scientific importance of FLNB Gene Knockout Cell Lines is underscored by their applications in both fundamental research and translational medicine. They serve as invaluable tools for drug screening, gene therapy exploration, and understandings of developmental biology. Furthermore, they provide a platform for investigating the role of filamin B in mechanotransduction and its contribution to diseases such as osteogenesis imperfecta and cardiovascular disorders.

Uniquely, FLNB Gene Knockout Cell Lines offer researchers a validated and ongoing resource that is often more reliable than transient knockdown methods. Because gene knockout yields stable genetic modifications, researchers can produce reproducible results over extended experiments. Compared to traditional methods like RNA interference, FLNB knockout lines support a clearer interpretation of data with less variability, enhancing experimental rigor.

These characteristics make FLNB Gene Knockout Cell Lines an essential asset for researchers and clinicians aiming to deepen their understanding of cellular mechanics and associated disease pathways. At our company, we pride ourselves on delivering high-quality, rigorously validated biological products that empower the scientific community, ensuring researchers have access to the tools they need to advance their work effectively.

Please note that all services are for research use only. Not intended for any clinical use.

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