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PRNP Knockout Cell Lines

Gene: PRNP

Official Full Name: prion protein (Kanno blood group)provided by HGNC

Gene Summary: The protein encoded by this gene is a membrane glycosylphosphatidylinositol-anchored glycoprotein that tends to aggregate into rod-like structures. The encoded protein contains a highly unstable region of five tandem octapeptide repeats. This gene is found on chromosome 20, approximately 20 kbp upstream of a gene which encodes a biochemically and structurally similar protein to the one encoded by this gene. Mutations in the repeat region as well as elsewhere in this gene have been associated with Creutzfeldt-Jakob disease, fatal familial insomnia, Gerstmann-Straussler disease, Huntington disease-like 1, and kuru. An overlapping open reading frame has been found for this gene that encodes a smaller, structurally unrelated protein, AltPrp. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO00885 PRNP Knockout cell line(A549) Human PRNP 1:3~1:4 Negative Online Inquiry
KO14879 PRNP Knockout cell line (HeLa) Human PRNP 1:3~1:6 Negative Online Inquiry
KO14880 PRNP Knockout cell line (HCT 116) Human PRNP 1:2~1:4 Negative Online Inquiry
KO14881 PRNP Knockout cell line (HEK293) Human PRNP 1:3~1:6 Negative Online Inquiry

Background

PRNP Gene Knockout Cell Lines are specially engineered cellular models where the prion protein gene (PRNP) has been completely inactivated. This precise genetic alteration enables scientists to study the function of the prion protein and its involvement in neurodegenerative diseases, particularly prion diseases such as Creutzfeldt-Jakob Disease. By removing the PRNP gene, these knockout cell lines provide an essential platform to investigate the molecular pathways affected by the absence of the prion protein, allowing for more targeted research into disease mechanisms.

The key function of PRNP Gene Knockout Cell Lines lies in their ability to serve as controlled environments to explore prion biology and pathology. They facilitate the examination of cellular responses to external prion protein exposure and help delineate the roles of prions in neurodegeneration. Furthermore, researchers can assess the interaction of other proteins with cellular processes when prion functions are disrupted, offering insights into synaptic maintenance and neurotoxic pathways.

In addition to their fundamental research applications, these knockout cell lines hold significant clinical relevance. They can be employed in drug discovery, allowing researchers to screen potential therapeutic compounds that could mitigate the effects of aberrant prion proteins. This innovation is particularly compelling given the lack of effective treatments for prion diseases, underscoring the critical need for novel therapeutic strategies.

One of the standout advantages of using our PRNP Gene Knockout Cell Lines is the rigor and reproducibility they offer compared to traditional models. Unlike non-specific cell lines or animal models, which often exhibit variability, our knockout lines provide consistent results, greatly enhancing data reliability. This precision aids in refining experimental designs and accelerates the pace of scientific discovery.

For researchers and clinicians specializing in neurodegenerative diseases, the value of PRNP Gene Knockout Cell Lines is immeasurable. They not only enable a deeper understanding of prion biology but also pave the way for innovative research that could lead to meaningful advancements in treatment.

At our company, we pride ourselves on being at the forefront of biotechnological advancements, offering expertly validated products designed to meet the rigorous demands of modern scientific inquiry. Our commitment to quality and innovation ensures that researchers have access to the best tools available for exploring the complexities of prion-related diseases.

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

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