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PFKM Knockout Cell Lines

Gene: PFKM

Official Full Name: phosphofructokinase, muscleprovided by HGNC

Gene Summary: Three phosphofructokinase isozymes exist in humans: muscle, liver and platelet. These isozymes function as subunits of the mammalian tetramer phosphofructokinase, which catalyzes the phosphorylation of fructose-6-phosphate to fructose-1,6-bisphosphate. Tetramer composition varies depending on tissue type. This gene encodes the muscle-type isozyme. Mutations in this gene have been associated with glycogen storage disease type VII, also known as Tarui disease. Alternatively spliced transcript variants have been described.[provided by RefSeq, Nov 2009]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO01048 PFKM Knockout cell line (HeLa) Human PFKM 1:3~1:6 Negative Online Inquiry
KO08257 PFKM Knockout cell line (HCT 116) Human PFKM 1:2~1:4 Negative Online Inquiry
KO08258 PFKM Knockout cell line (HEK293) Human PFKM 1:3~1:6 Negative Online Inquiry
KO08259 PFKM Knockout cell line (A549) Human PFKM 1:3~1:4 Negative Online Inquiry

Background

PFKM Gene Knockout Cell Lines are specialized cell lines developed through the targeted disruption of the phosphofructokinase, muscle (PFKM) gene, which plays a crucial role in glycolysis and energy metabolism. This innovative cellular tool allows researchers to investigate the metabolic pathways and physiological mechanisms influenced by PFKM. By implementing techniques such as CRISPR-Cas9 gene editing, these cell lines efficiently facilitate the study of PFKM function and its implications in various physiological and pathological contexts.

The primary function of PFKM Gene Knockout Cell Lines revolves around their ability to provide insights into the glycolytic pathway's regulation and its contribution to energy homeostasis. With PFKM being a key regulatory enzyme in converting fructose-6-phosphate to fructose-1,6-bisphosphate, the knockout models serve as critical resources to elucidate its functions in muscle metabolism and its potential roles in conditions like diabetes and certain muscle disorders. Researchers can leverage these models to explore the cellular adaptations that occur in the absence of PFKM, leading to the identification of novel therapeutic targets.

The scientific importance of PFKM Gene Knockout Cell Lines extends beyond metabolic research to impact areas such as cancer biology, where altered glycolysis plays a significant role in tumorigenesis. The ability to analyze the metabolic reprogramming in these cell lines provides valuable data for understanding disease mechanisms and developing targeted treatments.

What sets our PFKM Gene Knockout Cell Lines apart from alternatives is their validated functionality and consistency in experimental outcomes, which enhances reproducibility and reliability in research. Compared to other models, our cell lines are tailored specifically for studies involving glycolysis and metabolic dysfunctions, making them an indispensable resource for both academic and clinical researchers.

Incorporating PFKM Gene Knockout Cell Lines into your research toolkit furthers the understanding of critical biological processes, enabling significant advancements in the fight against metabolic diseases. As a leader in the development of innovative biological products, our company is committed to providing high-quality cell lines and resources that empower researchers and clinicians to achieve breakthroughs in their fields.

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

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