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INSIG1 Knockout Cell Lines

Gene: INSIG1

Official Full Name: insulin induced gene 1provided by HGNC

Gene Summary: This gene encodes an endoplasmic reticulum membrane protein that regulates cholesterol metabolism, lipogenesis, and glucose homeostasis. The encoded protein has six transmembrane helices which contain an effector protein binding site. It binds the sterol-sensing domains of sterol regulatory element-binding protein (SREBP) cleavage-activating protein (SCAP) and 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMG-CoA reductase), and is essential for the sterol-mediated trafficking of these two proteins. It promotes the endoplasmic reticulum retention of SCAP and the ubiquitin-mediated degradation of HMG-CoA reductase. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2016]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO37044 INSIG1 Knockout cell line (HeLa) Human INSIG1 1:3~1:6 Negative Online Inquiry
KO37045 INSIG1 Knockout cell line (HCT 116) Human INSIG1 1:2~1:4 Negative Online Inquiry
KO37046 INSIG1 Knockout cell line (HEK293) Human INSIG1 1:3~1:6 Negative Online Inquiry
KO37047 INSIG1 Knockout cell line (A549) Human INSIG1 1:3~1:4 Negative Online Inquiry

Background

INSIG1 Gene Knockout Cell Lines are specialized human cell lines that have been genetically engineered to lack the expression of the insulin-induced gene 1 (INSIG1), a vital regulatory gene involved in cholesterol metabolism and lipid homeostasis. These cell lines serve as crucial tools for studying the biological role of INSIG1 in cellular processes such as lipid synthesis, endoplasmic reticulum stress, and membrane trafficking. By utilizing CRISPR/Cas9 technology, researchers can achieve precise gene disruptions, allowing for in-depth analysis of the downstream effects of INSIG1 depletion in various physiological and pathological contexts.

The key functions of INSIG1 involve its interaction with membrane proteins such as SREBP (Sterol Regulatory Element-Binding Proteins) that regulate cholesterol and fatty acid synthesis. In the absence of INSIG1, cells undergo significant alterations in lipid metabolism, providing a unique opportunity to investigate lipid-related disease mechanisms, such as obesity, diabetes, and cardiovascular diseases. The use of these knockout cell lines in research has been pivotal, facilitating the exploration of novel therapeutic targets and drug screening approaches.

Compared to alternative models, INSIG1 Gene Knockout Cell Lines offer distinct advantages including increased specificity and relevance to human physiology. The precise gene editing enables a more controlled experimental environment, reducing variability and enhancing the reliability of experimental outcomes. Additionally, these cell lines are compatible with high-throughput screening techniques, allowing researchers to quickly assess the impact of different compounds on lipid metabolic pathways.

For researchers and clinicians focusing on metabolic diseases, the INSIG1 Gene Knockout Cell Lines provide an invaluable resource for understanding disease mechanisms and testing potential therapeutic strategies. Their deployment in clinical studies or drug discovery processes can accelerate the advancement of treatment options for conditions related to dysregulated lipid metabolism.

As a company at the forefront of genetic engineering and cell line development, we pride ourselves on our commitment to providing high-quality, precisely crafted biological models that empower researchers to make significant advancements in their fields. Our expertise ensures that our products meet the highest scientific standards, allowing our users to push the boundaries of biological research.

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

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