Gene: IDE
Official Full Name: insulin degrading enzymeprovided by HGNC
Gene Summary: This gene encodes a zinc metallopeptidase that degrades intracellular insulin, and thereby terminates insulins activity, as well as participating in intercellular peptide signalling by degrading diverse peptides such as glucagon, amylin, bradykinin, and kallidin. The preferential affinity of this enzyme for insulin results in insulin-mediated inhibition of the degradation of other peptides such as beta-amyloid. Deficiencies in this protein's function are associated with Alzheimer's disease and type 2 diabetes mellitus but mutations in this gene have not been shown to be causitive for these diseases. This protein localizes primarily to the cytoplasm but in some cell types localizes to the extracellular space, cell membrane, peroxisome, and mitochondrion. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional transcript variants have been described but have not been experimentally verified.[provided by RefSeq, Sep 2009]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO37128 | IDE Knockout cell line (HeLa) | Human | IDE | 1:3~1:6 | Negative | Online Inquiry |
KO37129 | IDE Knockout cell line (HCT 116) | Human | IDE | 1:2~1:4 | Negative | Online Inquiry |
KO37130 | IDE Knockout cell line (HEK293) | Human | IDE | 1:3~1:6 | Negative | Online Inquiry |
KO37131 | IDE Knockout cell line (A549) | Human | IDE | 1:3~1:4 | Negative | Online Inquiry |
IDE Gene Knockout Cell Lines are genetically engineered cell lines specifically designed to lack the expression of the insulin-degrading enzyme (IDE). IDE plays a pivotal role in the regulation of insulin levels by degrading excess insulin and amyloid-beta peptides, which are implicated in metabolic disorders and neurodegenerative diseases, such as Alzheimer's disease. By using CRISPR/Cas9 or similar gene-editing technologies, these cell lines are created to enable researchers to investigate the biochemical pathways associated with IDE function and its impact on various physiological conditions.
The primary function of IDE Gene Knockout Cell Lines lies in their ability to elucidate the biological effects resulting from the absence of IDE, offering insights into its role in insulin sensitivity and amyloid pathology. Researchers can use these knockout cell lines to study the consequences of altered IDE activity on glucose metabolism, amyloid aggregation, and overall cellular health. This mechanistic understanding can springboard further investigation into targeted therapies for conditions such as diabetes and Alzheimer's disease.
The scientific importance of IDE Gene Knockout Cell Lines is profound, as they serve as a critical tool for both basic and applied research. In clinical settings, these cell lines can facilitate the development of new drugs aimed at modulating insulin levels or reducing amyloid accumulation, potentially leading to innovative treatments for metabolic syndromes and neurodegenerative conditions.
What sets IDE Gene Knockout Cell Lines apart from traditional cell models is their specificity and precision. Unlike general cell lines that may express IDE variably, these knockout lines provide a consistent and reliable model to study the direct effects of IDE knockout, enhancing reproducibility in experimental designs. This specificity minimizes confounding variables, allowing for clearer conclusions and more robust data.
For researchers and clinicians, the availability of IDE Gene Knockout Cell Lines provides an invaluable resource to accelerate the understanding of insulin regulation and amyloid pathogenesis, ultimately contributing to the advancement of personalized medicine and therapeutic interventions.
Our company prides itself on its dedication to producing high-quality, precision-engineered biological products, ensuring that our IDE Gene Knockout Cell Lines meet the rigorous standards required in cutting-edge scientific research.
Please note that all services are for research use only. Not intended for any clinical use.
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