Gene: NR1D2
Official Full Name: nuclear receptor subfamily 1 group D member 2provided by HGNC
Gene Summary: This gene encodes a member of the nuclear hormone receptor family, specifically the NR1 subfamily of receptors. The encoded protein functions as a transcriptional repressor and may play a role in circadian rhythms and carbohydrate and lipid metabolism. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2009]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO32430 | NR1D2 Knockout cell line (HeLa) | Human | NR1D2 | 1:3~1:6 | Negative | Online Inquiry |
KO32431 | NR1D2 Knockout cell line (HCT 116) | Human | NR1D2 | 1:2~1:4 | Negative | Online Inquiry |
KO32432 | NR1D2 Knockout cell line (HEK293) | Human | NR1D2 | 1:3~1:6 | Negative | Online Inquiry |
KO32433 | NR1D2 Knockout cell line (A549) | Human | NR1D2 | 1:3~1:4 | Negative | Online Inquiry |
NR1D2 Gene Knockout Cell Lines are genetically engineered cell lines designed to eliminate the expression of the NR1D2 gene (Nuclear Receptor Subfamily 1 Group D Member 2), a crucial regulator of circadian rhythms and metabolic processes. By precisely disrupting the NR1D2 gene, these cell lines allow researchers to study the gene's functional roles and the resultant physiological impacts, particularly in relation to circadian biology, metabolism, and cell cycle regulation.
The key function of NR1D2 is its involvement in the modulation of transcriptional networks governing circadian rhythms, thus influencing metabolic homeostasis. By utilizing these knockout cell lines, scientists can investigate the downstream effects of NR1D2 depletion on gene expression, cellular metabolism, and overall cellular behavior. Through techniques such as RNA sequencing and metabolomic profiling, researchers gain insights into how disruptions in circadian regulation can contribute to various disorders, including obesity, diabetes, and cardiovascular diseases.
The scientific importance of NR1D2 Gene Knockout Cell Lines extends into both research and clinical applications. In research settings, these cell lines provide a robust model for studying clock-controlled genes and their contributions to chronic conditions tied to metabolic dysregulation. Clinically, understanding NR1D2’s role may open new avenues for therapeutic interventions aimed at restoring circadian balance and tackling metabolic disorders.
What sets NR1D2 Gene Knockout Cell Lines apart from traditional experimental models is their precise gene targeting and customized control over genetic expression. Unlike conventional models that may present background variability, these cell lines offer a homogenous population for reproducible results, thereby enhancing experimental rigor and reliability.
The value of these cell lines is significant for researchers and clinicians seeking to unravel the complexities of circadian biology and its implications on health. By leveraging NR1D2 Gene Knockout Cell Lines, users can deepen their understanding of chronobiology and metabolic diseases, facilitating the discovery of novel therapeutic strategies.
Our company is committed to providing high-quality biological products that empower researchers to advance scientific understanding. With a focus on precision gene editing technologies and a dedication to innovation, we are positioned as leaders in the field, ensuring that our products meet the highest standards of scientific integrity and utility.
Please note that all services are for research use only. Not intended for any clinical use.
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