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RING1 Knockout Cell Lines

Gene: RING1

Official Full Name: ring finger protein 1provided by HGNC

Gene Summary: This gene belongs to the RING finger family, members of which encode proteins characterized by a RING domain, a zinc-binding motif related to the zinc finger domain. The gene product can bind DNA and can act as a transcriptional repressor. It is associated with the multimeric polycomb group protein complex. The gene product interacts with the polycomb group proteins BMI1, EDR1, and CBX4, and colocalizes with these proteins in large nuclear domains. It interacts with the CBX4 protein via its glycine-rich C-terminal domain. The gene maps to the HLA class II region, where it is contiguous with the RING finger genes FABGL and HKE4. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO35618 RING1 Knockout cell line (HeLa) Human RING1 1:3~1:6 Negative Online Inquiry
KO35619 RING1 Knockout cell line (HCT 116) Human RING1 1:2~1:4 Negative Online Inquiry
KO35620 RING1 Knockout cell line (HEK293) Human RING1 1:3~1:6 Negative Online Inquiry
KO35621 RING1 Knockout cell line (A549) Human RING1 1:3~1:4 Negative Online Inquiry

Background

RING1 Gene Knockout Cell Lines are genetically engineered cell lines designed to exhibit a complete loss of function of the RING1 gene, which plays a pivotal role in epigenetic regulation through the Polycomb Repressive Complex 1 (PRC1). The RING1 protein is crucial for maintaining stem cell characteristics and regulating gene expression during development. By utilizing advanced CRISPR/Cas9 technology, these knockout cell lines provide researchers with a robust platform for studying the downstream effects of RING1 absence at the cellular and molecular levels.

The primary function of RING1 gene knockout is to facilitate the examination of mechanistic pathways affected by its deletion, particularly in relation to chromatin remodeling and transcriptional repression. This opens avenues for exploring RING1's influence on cell fate decisions, differentiation processes, and oncogenesis. Furthermore, the depletion of RING1 allows researchers to probe its interactions with various epigenetic modifiers and to understand how these interactions impact cellular behavior in both normal and pathological contexts.

The scientific significance of RING1 Gene Knockout Cell Lines is underscored by their applications in genetic, developmental, and cancer research. They can serve as models for investigating diseases where epigenetic regulation is disrupted, such as various cancers and developmental disorders. Additionally, these cell lines offer a valuable asset for drug discovery efforts, permitting researchers to assess the efficacy of therapeutic compounds targeting epigenetic pathways.

What sets RING1 Gene Knockout Cell Lines apart is their precision in gene editing and the stability of the knockout phenotype across multiple passages. Compared to traditional knockdown approaches using RNA interference, these cell lines provide a more permanent solution, ensuring reproducibility and reliability in experimental design. This guarantees that researchers can draw meaningful conclusions without the confounding effects associated with transient gene silencing.

For researchers and clinicians focused on unraveling the complexities of gene regulation and cellular dynamics, RING1 Gene Knockout Cell Lines are an invaluable tool. They offer clarity in experiments aimed at elucidating fundamental biological processes and generating insights that could lead to therapeutic advancements.

At our company, we are dedicated to providing high-quality, validated biological products that empower the scientific community. With our expertise in genetic engineering and cellular biology, we are committed to advancing research that shapes the future of medicine and biotechnology.

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

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