Gene: APP
Official Full Name: amyloid beta precursor proteinprovided by HGNC
Gene Summary: This gene encodes a cell surface receptor and transmembrane precursor protein that is cleaved by secretases to form a number of peptides. Some of these peptides are secreted and can bind to the acetyltransferase complex APBB1/TIP60 to promote transcriptional activation, while others form the protein basis of the amyloid plaques found in the brains of patients with Alzheimer disease. In addition, two of the peptides are antimicrobial peptides, having been shown to have bacteriocidal and antifungal activities. Mutations in this gene have been implicated in autosomal dominant Alzheimer disease and cerebroarterial amyloidosis (cerebral amyloid angiopathy). Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Aug 2014]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO02727 | APP Knockout cell line (HeLa) | Human | APP | 1:3~1:6 | Negative | Online Inquiry |
KO02728 | APP Knockout cell line (HCT 116) | Human | APP | 1:2~1:4 | Negative | Online Inquiry |
KO02729 | APP Knockout cell line (HEK293) | Human | APP | 1:3~1:6 | Negative | Online Inquiry |
KO02730 | APP Knockout cell line (A549) | Human | APP | 1:3~1:4 | Negative | Online Inquiry |
APP Gene Knockout Cell Lines are specifically engineered cell lines in which the amyloid precursor protein (APP) gene has been inactivated through precise gene-editing techniques. This innovative biological product serves as a vital tool for researchers studying Alzheimer's disease and other neurodegenerative disorders tied to APP metabolism. By eliminating the expression of APP, these cell lines provide a controlled environment for investigating the biological consequences of APP deficiency, including alterations in cellular signaling, neurotransmission, and amyloid beta peptide production.
The key function of APP Gene Knockout Cell Lines lies in their ability to facilitate in-depth analyses of neurobiological pathways. Researchers can utilize these models to explore the implications of APP loss on synaptic function and neuronal health, allowing for the identification of potential therapeutic targets. The mechanism involves gene silencing through CRISPR/Cas9 or similar genome-editing technologies, ensuring specificity and efficiency in the knockout process.
The scientific importance of APP Gene Knockout Cell Lines is underscored by their application in both basic and translational research settings. They play a crucial role in the development of Alzheimer's therapeutics, providing insights into disease mechanisms and aiding in the evaluation of drug candidates. Furthermore, these cell lines can serve as platforms for high-throughput screening of compounds that could mitigate APP-related pathologies.
Compared to alternative models, such as wild-type cell lines or non-human systems, APP Gene Knockout Cell Lines offer enhanced specificity for studying APP-related phenomena. Their defined genetic background minimizes variability and allows for more reproducible results, which is critical in establishing robust scientific findings. Additionally, the availability of various knockout variants enhances their utility in dissecting the multifaceted roles of APP in cellular biology.
For researchers and clinicians dedicated to unraveling the complexities of neurodegenerative diseases, APP Gene Knockout Cell Lines represent a valuable resource. Their ability to provide mechanistic insights into APP-related pathways makes them indispensable for both hypothesis-driven research and drug discovery efforts.
At [Your Company Name], we pride ourselves on our expertise in creating high-quality biological research products. Our APP Gene Knockout Cell Lines are developed using state-of-the-art technology, backed by comprehensive validation to guarantee performance and reliability in your experimental designs.
Please note that all services are for research use only. Not intended for any clinical use.
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