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RTN3 Knockout Cell Lines

Gene: RTN3

Official Full Name: reticulon 3provided by HGNC

Gene Summary: This gene belongs to the reticulon family of highly conserved genes that are preferentially expressed in neuroendocrine tissues. This family of proteins interact with, and modulate the activity of beta-amyloid converting enzyme 1 (BACE1), and the production of amyloid-beta. An increase in the expression of any reticulon protein substantially reduces the production of amyloid-beta, suggesting that reticulon proteins are negative modulators of BACE1 in cells. Alternatively spliced transcript variants encoding different isoforms have been found for this gene, and pseudogenes of this gene are located on chromosomes 4 and 12. [provided by RefSeq, May 2012]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO06289 RTN3 Knockout cell line (HeLa) Human RTN3 1:3~1:6 Negative Online Inquiry
KO06290 RTN3 Knockout cell line (HCT 116) Human RTN3 1:2~1:4 Negative Online Inquiry
KO06291 RTN3 Knockout cell line (HEK293) Human RTN3 1:3~1:6 Negative Online Inquiry
KO06292 RTN3 Knockout cell line (A549) Human RTN3 1:3~1:4 Negative Online Inquiry

Background

RTN3 Gene Knockout Cell Lines represent a groundbreaking advancement in cellular biology, enabling researchers to investigate the functional roles of the Reticulon 3 (RTN3) protein in various biological processes. These cell lines are genetically engineered to lack the RTN3 gene, allowing for in-depth studies of its implications in neurodegenerative diseases, cellular stress responses, and autophagy pathways. By providing a controlled environment devoid of RTN3, researchers can dissect the protein's role in the endoplasmic reticulum's structure and function, thereby contributing to a greater understanding of cellular homeostasis.

The mechanism of action for RTN3 Gene Knockout Cell Lines involves the deletion of the RTN3 gene through precise CRISPR-Cas9 technology, leading to observable phenotypic changes that can be quantified. This strategy not only allows for targeted analyses of RTN3’s loss-of-function effects but also facilitates the exploration of compensatory mechanisms that might be activated in its absence. As a result, these cell lines serve as robust systems for studying gene function, drug responses, and potential therapeutic targets, particularly in neurobiology and cancer research.

The scientific importance of RTN3 Gene Knockout Cell Lines lies in their ability to illuminate pathways that may contribute to pathology in the central nervous system and other tissues. In a clinical context, understanding RTN3's role could pave the way for novel treatment strategies aimed at neurodegenerative disorders or cellular stress-related conditions. Furthermore, these cell lines are essential for drug discovery and the evaluation of therapeutic interventions.

Compared to alternative approaches, such as traditional siRNA knockdown methods or overexpression systems, the RTN3 Gene Knockout Cell Lines provide a stable and permanent alteration of the gene. This stability allows for long-term studies and reduces variability, thus offering more reliable data for experimental reproducibility.

For researchers, clinicians, and pharmaceutical developers alike, the value of RTN3 Gene Knockout Cell Lines is clear: they enable advanced biological insights and foster the development of precise therapeutic strategies. Our company, recognized for its commitment to providing high-quality genetic products, ensures that these cell lines are validated for performance and consistency, empowering your research endeavors with confidence.

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

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