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PPARG Knockout Cell Lines

Gene: PPARG

Official Full Name: peroxisome proliferator activated receptor gammaprovided by HGNC

Gene Summary: This gene encodes a member of the peroxisome proliferator-activated receptor (PPAR) subfamily of nuclear receptors. PPARs form heterodimers with retinoid X receptors (RXRs) and these heterodimers regulate transcription of various genes. Three subtypes of PPARs are known: PPAR-alpha, PPAR-delta, and PPAR-gamma. The protein encoded by this gene is PPAR-gamma and is a regulator of adipocyte differentiation. Additionally, PPAR-gamma has been implicated in the pathology of numerous diseases including obesity, diabetes, atherosclerosis and cancer. Alternatively spliced transcript variants that encode different isoforms have been described. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO09328 PPARG Knockout cell line (HeLa) Human PPARG 1:3~1:6 Negative Online Inquiry
KO09329 PPARG Knockout cell line (HCT 116) Human PPARG 1:2~1:4 Negative Online Inquiry
KO09330 PPARG Knockout cell line (HEK293) Human PPARG 1:3~1:6 Negative Online Inquiry
KO09331 PPARG Knockout cell line (A549) Human PPARG 1:3~1:4 Negative Online Inquiry

Background

PPARG Gene Knockout Cell Lines are genetically engineered cell lines in which the peroxisome proliferator-activated receptor gamma (PPARG) gene has been specifically disrupted or "knocked out." These cell lines serve as essential tools for researchers studying metabolic syndromes, obesity, and various types of cancer, particularly because PPARG plays a crucial role in adipocyte differentiation and insulin sensitivity. By utilizing these knockout cell lines, scientists are able to investigate the downstream effects of PPARG loss, examining alterations in cellular pathways that contribute to metabolic dysfunction and other pathologies.

The primary function of PPARG consists of acting as a transcription factor that regulates the expression of genes involved in glucose and lipid metabolism. In a typical setting, the activation of PPARG influences adipocyte formation and insulin signaling pathways. When these cell lines are employed, researchers can focus on studying the impact of PPARG deactivation on metabolic rate, fat accumulation, and responses to therapeutic agents, thereby elucidating its role in disease mechanisms.

The scientific importance of these knockout cell lines is reflected in their wide-ranging applications in both research and clinical settings. They enable detailed exploration of the PPARG protein's involvement in metabolic diseases and could support the identification of novel therapeutic targets for conditions like type 2 diabetes and cardiovascular disorders. These tools are invaluable for drug discovery and understanding disease pathways, offering insights critical for developing new pharmacological interventions.

Compared to traditional research models, PPARG Gene Knockout Cell Lines offer several advantages, including heightened specificity and the ability to control experimental conditions more precisely. Unlike whole organisms or non-specific cellular models, these knockout lines provide a clearer picture of the PPARG-dependent pathways, leading to more reliable and reproducible results.

For researchers, clinicians, and pharmaceutical developers focused on metabolic health, these cell lines represent a significant step toward advancing our understanding of complex biological interactions. Their value lies not only in enabling groundbreaking research but also in the capacity to aid in the development of targeted therapies that can mitigate the impact of metabolic disorders.

Our company specializes in providing high-quality, genetically modified biological products, and we are committed to supporting the scientific community with tools that push the boundaries of current research. With a focus on precision and reproducibility, our PPARG Gene Knockout Cell Lines are designed to meet the rigorous demands of modern laboratory needs.

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

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