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CUL3 Knockout Cell Lines

Gene: CUL3

Official Full Name: cullin 3provided by HGNC

Gene Summary: This gene encodes a member of the cullin protein family. The encoded protein plays a critical role in the polyubiquitination and subsequent degradation of specific protein substrates as the core component and scaffold protein of an E3 ubiquitin ligase complex. Complexes including the encoded protein may also play a role in late endosome maturation. Mutations in this gene are a cause of type 2E pseudohypoaldosteronism. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Mar 2012]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO00162 CUL3 Knockout cell line (HCT 116) Human CUL3 1:2~1:4 Negative Online Inquiry
KO10081 CUL3 Knockout cell line (HeLa) Human CUL3 1:3~1:6 Negative Online Inquiry
KO10082 CUL3 Knockout cell line (HEK293) Human CUL3 1:3~1:6 Negative Online Inquiry
KO10083 CUL3 Knockout cell line (A549) Human CUL3 1:3~1:4 Negative Online Inquiry

Background

CUL3 Gene Knockout Cell Lines represent a groundbreaking tool in molecular and cellular biology, designed to facilitate the detailed study of the CUL3 gene's functions and its pivotal roles in various biological processes. CUL3, or Cullin 3, is a vital component of the ubiquitin-proteasome system that regulates protein degradation, thereby influencing cellular growth, apoptosis, and metabolism. Our cultured cell lines have been meticulously engineered to permanently knock out the CUL3 gene, allowing researchers to evaluate its impact on cellular pathways and to observe phenotypic changes that arise from this modification.

The primary function of the CUL3 Gene Knockout Cell Lines is to provide a robust experimental platform for examining the mechanisms by which CUL3 regulates substrate recognition and ubiquitination. By utilizing CRISPR/Cas9 technology, these cell lines possess a high specificity and efficiency for gene editing, which greatly enhances the reproducibility of the experiments. This gene knockout model is essential for investigating diseases linked to dysregulation in the ubiquitin-proteasome system, such as cancer, neurodegenerative disorders, and developmental abnormalities.

The scientific importance of these cell lines extends to both research and clinical applications, serving as a valuable resource for drug discovery, biomarker identification, and elucidating disease mechanisms. Moreover, they can be utilized in high-throughput screening assays to identify compounds that may restore normal CUL3 function or inhibit its deleterious effects.

What sets our CUL3 Gene Knockout Cell Lines apart from alternatives is their comprehensive characterizations and validation, ensuring that researchers can rely on them for highly specific experimental outcomes. Unlike other generic knockout models, our cell lines are rigorously developed and backed by extensive validation to confirm effective gene disruption and targeted loss of function.

Researchers, clinicians, and pharmaceutical companies will find immense value in these cell lines as they accelerate the understanding of CUL3-related pathways and offer insights into potential therapeutic targets. Our unwavering commitment to quality and innovation in biological products positions us as a leader in molecular biology advancements, enabling our customers to explore new frontiers in their research endeavors.

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

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