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SPEN Knockout Cell Lines

Gene: SPEN

Official Full Name: spen family transcriptional repressorprovided by HGNC

Gene Summary: This gene encodes a hormone inducible transcriptional repressor. Repression of transcription by this gene product can occur through interactions with other repressors, by the recruitment of proteins involved in histone deacetylation, or through sequestration of transcriptional activators. The product of this gene contains a carboxy-terminal domain that permits binding to other corepressor proteins. This domain also permits interaction with members of the NuRD complex, a nucleosome remodeling protein complex that contains deacetylase activity. In addition, this repressor contains several RNA recognition motifs that confer binding to a steroid receptor RNA coactivator; this binding can modulate the activity of both liganded and nonliganded steroid receptors. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO30026 SPEN Knockout cell line (HeLa) Human SPEN 1:3~1:6 Negative Online Inquiry
KO30027 SPEN Knockout cell line (HCT 116) Human SPEN 1:2~1:4 Negative Online Inquiry
KO30028 SPEN Knockout cell line (HEK293) Human SPEN 1:3~1:6 Negative Online Inquiry
KO30029 SPEN Knockout cell line (A549) Human SPEN 1:3~1:4 Negative Online Inquiry

Background

SPEN Gene Knockout Cell Lines are engineered cellular models designed to facilitate in-depth research into the function of the SPEN gene, a transcriptional regulator implicated in various biological processes and disease mechanisms, including those related to cellular differentiation and oncogenesis. These cell lines utilize advanced CRISPR/Cas9 genome-editing technology to achieve precise knockout of the SPEN gene, thereby providing a powerful tool for researchers aiming to unravel the gene's role in different cellular contexts.

The key functionality of SPEN Gene Knockout Cell Lines lies in their ability to enable scientists to examine the resulting phenotypic and molecular changes following the loss of SPEN expression. By employing these knockout models, researchers can investigate changes in gene expression profiles, signaling pathways, and cellular behavior, which are crucial for understanding the underlying mechanisms of various diseases such as cancer, neurodevelopmental disorders, and metabolic conditions. The precision of this gene editing not only allows for high reproducibility in experiments but also minimizes off-target effects, enhancing the reliability of research outcomes.

The scientific importance of SPEN Gene Knockout Cell Lines extends into both basic research and clinical application. In basic research, these cell lines serve as invaluable resources to explore gene function and regulatory networks. In clinical settings, understanding the implications of SPEN knockout may lead to novel therapeutic strategies, particularly in cancers where SPEN misregulation is observed.

Unlike traditional methods of gene disruption, such as RNA interference, SPEN Gene Knockout Cell Lines offer a permanent modification of the genome, providing sustainable and long-term insights into gene function. Furthermore, they are compatible with high-throughput screening methods, which accelerates the discovery process significantly. Researchers benefit from a more streamlined approach to experimental design with these robust cellular models, enhancing both efficiency and reproducibility in studies.

Designed for researchers and clinicians in the fields of molecular biology, oncology, and genetics, SPEN Gene Knockout Cell Lines represent a pivotal advancement in cellular research tools. Our company prides itself on providing high-quality, reliable biological products, backed by years of expertise in gene editing technologies, ensuring that our customers have access to the best resources available for their scientific endeavors.

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

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