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PCK2 Knockout Cell Lines

Gene: PCK2

Official Full Name: phosphoenolpyruvate carboxykinase 2, mitochondrialprovided by HGNC

Gene Summary: This gene encodes a mitochondrial enzyme that catalyzes the conversion of oxaloacetate to phosphoenolpyruvate in the presence of guanosine triphosphate (GTP). A cytosolic form of this protein is encoded by a different gene and is the key enzyme of gluconeogenesis in the liver. Alternatively spliced transcript variants have been described. [provided by RefSeq, Apr 2014]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO08150 PCK2 Knockout cell line (HeLa) Human PCK2 1:3~1:6 Negative Online Inquiry
KO08151 PCK2 Knockout cell line (HCT 116) Human PCK2 1:2~1:4 Negative Online Inquiry
KO08152 PCK2 Knockout cell line (HEK293) Human PCK2 1:3~1:6 Negative Online Inquiry
KO08153 PCK2 Knockout cell line (A549) Human PCK2 1:3~1:4 Negative Online Inquiry

Background

PCK2 Gene Knockout Cell Lines are genetically engineered cell lines in which the PCK2 gene has been selectively disrupted, resulting in a model that enables researchers to investigate the physiological and metabolic roles of this gene. PCK2, or phosphoenolpyruvate carboxykinase 2, is a vital enzyme involved in gluconeogenesis and plays a significant role in energy metabolism, particularly in the context of metabolic disorders. By utilizing these knockout cell lines, researchers can elucidate the molecular mechanisms of PCK2's involvement in cellular processes such as glucose production, lipid metabolism, and cellular signaling pathways.

The primary mechanism of action for these knockout cell lines lies in their ability to mimic pathological conditions, effectively allowing researchers to dissect the contribution of PCK2 to various metabolic diseases, including obesity, diabetes, and cancer. By analyzing the altered metabolic profiles and gene expressions in the absence of PCK2, scientists can ascertain its potential as a therapeutic target, opening avenues for novel treatment strategies.

In terms of scientific importance, PCK2 Gene Knockout Cell Lines have wide-ranging applications in both research and clinical settings. They facilitate the understanding of metabolic syndromes and provide a platform for drug discovery processes that target enzymatic pathways associated with glucose and lipid metabolism. Moreover, the ability to study the ramifications of PCK2 deficiency can yield insights into potential biomarkers for disease states, advancing precision medicine.

The distinct advantage of PCK2 Gene Knockout Cell Lines over alternative models is their specificity and reproducibility, ensuring that results are consistent and reliable. Conventional cell lines may not accurately reflect the metabolic disruptions that occur in vivo; however, these knockout models provide a more authentic representation of the effects of PCK2 gene depletion, making them invaluable for targeted research applications.

For researchers, clinicians, and pharmaceutical companies focused on proprietary approaches to metabolic disorders, PCK2 Gene Knockout Cell Lines represent a critical resource for advancing understanding and therapy. Our company, a leader in the field of genetic engineering and cell line development, is committed to equipping scientists with high-quality tools that translate into meaningful breakthroughs in metabolic research and therapy design.

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

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