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FKRP Knockout Cell Lines

Gene: FKRP

Official Full Name: fukutin related proteinprovided by HGNC

Gene Summary: This gene encodes a protein which is targeted to the medial Golgi apparatus and is necessary for posttranslational modification of dystroglycan. Mutations in this gene have been associated with congenital muscular dystrophy, cognitive disability, and cerebellar cysts. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Oct 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO20488 FKRP Knockout cell line (HeLa) Human FKRP 1:3~1:6 Negative Online Inquiry
KO20489 FKRP Knockout cell line (HCT 116) Human FKRP 1:2~1:4 Negative Online Inquiry
KO20490 FKRP Knockout cell line (HEK293) Human FKRP 1:3~1:6 Negative Online Inquiry
KO20491 FKRP Knockout cell line (A549) Human FKRP 1:3~1:4 Negative Online Inquiry

Background

FKRP Gene Knockout Cell Lines represent a crucial advancement in the study of muscular dystrophies and associated genetic disorders. These engineered cell lines feature the targeted disruption of the FKRP gene, which encodes a protein vital for the proper glycosylation of dystroglycan, a key component of the muscle cell membrane. The knockout of this gene allows researchers to investigate its specific role in cellular processes and disease mechanisms, particularly in relation to congenital muscular dystrophy and other dystroglycanopathies.

The primary function of FKRP Gene Knockout Cell Lines revolves around their ability to facilitate the in-depth study of FKRP-dependent biological pathways. By illustrating how the absence of this gene affects muscle cell integrity, signaling cascades, and overall cellular function, these cell lines serve as powerful tools in elucidating the molecular underpinnings of muscle degeneration and repair processes. Furthermore, the cell lines can be utilized for high-throughput screening of potential therapeutics, providing a platform for drug discovery targeted at restoring glycosylation pathways impaired in disease states.

The scientific importance of these cell lines is underscored by their utility in both basic and translational research. They offer invaluable insights not just into FKRP's role in muscular conditions but also into broader applications in gene therapy development and precision medicine strategies. Unlike traditional models, FKRP Gene Knockout Cell Lines provide a more accurate representation of human disease mechanisms, empowering researchers to develop targeted interventions that address specific pathways affected by FKRP deficiency.

Comparatively, FKRP Gene Knockout Cell Lines outshine standard cell lines and animal models due to their precise genetic modification and human-derived origin. This specificity allows for higher relevance in translating findings from the lab to potential clinical applications, which is often a challenge in less targeted models. Additionally, these specialized lines save time and resources in the research process, enabling quicker and more reliable results.

The value of FKRP Gene Knockout Cell Lines to researchers, clinicians, and pharmaceutical developers is immense; they not only enhance our understanding of fundamental biological processes but also pave the way for innovative treatments for genetic disorders that have long been deemed challenging targets.

Our company prides itself on its expertise in developing high-quality biological products, with a commitment to advancing research tools that empower scientists in the quest for novel therapies. Our FKRP Gene Knockout Cell Lines embody this mission, offering state-of-the-art resources for the scientific community.

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

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