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PYGB Knockout Cell Lines

Gene: PYGB

Official Full Name: glycogen phosphorylase Bprovided by HGNC

Gene Summary: The protein encoded by this gene is a glycogen phosphorylase found predominantly in the brain. The encoded protein forms homodimers which can associate into homotetramers, the enzymatically active form of glycogen phosphorylase. The activity of this enzyme is positively regulated by AMP and negatively regulated by ATP, ADP, and glucose-6-phosphate. This enzyme catalyzes the rate-determining step in glycogen degradation. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO35741 PYGB Knockout cell line (HeLa) Human PYGB 1:3~1:6 Negative Online Inquiry
KO35742 PYGB Knockout cell line (HCT 116) Human PYGB 1:2~1:4 Negative Online Inquiry
KO35743 PYGB Knockout cell line (HEK293) Human PYGB 1:3~1:6 Negative Online Inquiry
KO35744 PYGB Knockout cell line (A549) Human PYGB 1:3~1:4 Negative Online Inquiry

Background

PYGB Gene Knockout Cell Lines are advanced cellular models designed specifically for the functional study of the PYGB gene, which encodes the muscle-specific glycogen phosphorylase enzyme. These engineered cell lines have been generated by utilizing CRISPR/Cas9 technology to achieve precise gene editing, ensuring the complete disruption of PYGB expression. By depleting the cellular machinery responsible for glycogen metabolism, these cell lines provide a unique opportunity to investigate the metabolic pathways and biological processes directly influenced by this gene.

The primary function of PYGB Gene Knockout Cell Lines is to serve as a robust tool for studying the effects of PYGB deficiency on glycogen metabolism and cellular energy homeostasis. By creating a knockout model, researchers can explore how the absence of this enzyme impacts muscle physiology, energy retrieval, and even links to metabolic disorders such as diabetes and glycogen storage diseases. Through experiments utilizing these cell lines, scientists can elucidate the signaling pathways involved in muscle energy metabolism, paving the way for novel therapeutic strategies.

The scientific importance of these cell lines extends to both basic research and clinical applications. In basic research, they facilitate a deeper understanding of metabolic diseases, while in the clinical landscape, they offer insights into potential gene therapies or pharmaceutical interventions aimed at restoring normal metabolic function in patients with PYGB-related disorders.

What sets PYGB Gene Knockout Cell Lines apart from conventional cellular models is their precision and the reliability of gene editing. Unlike previous methods that may yield incomplete knockouts, CRISPR/Cas9 technology ensures virtually complete gene ablation, significantly reducing variability in experimental results. This enhancement translates to more confident and reproducible data, empowering researchers to draw meaningful conclusions from their studies.

For researchers and clinicians focusing on metabolic diseases and muscle disorders, these cell lines represent an invaluable resource. By leveraging the advanced understanding provided by our PYGB Gene Knockout Cell Lines, users can accelerate their research and develop innovative solutions for metabolic health challenges.

Our company, committed to excellence in biological research tools, provides a suite of specialized models like the PYGB Gene Knockout Cell Lines, reflecting our deep expertise in gene editing technologies and their applications in cutting-edge scientific inquiry.

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

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