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SMARCD2 Knockout Cell Lines

Gene: SMARCD2

Official Full Name: SWI/SNF related BAF chromatin remodeling complex subunit D2provided by HGNC

Gene Summary: The protein encoded by this gene is a member of the SWI/SNF family of proteins, whose members display helicase and ATPase activities and which are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI and has sequence similarity to the yeast Swp73 protein. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO00931 SMARCD2 Knockout cell line(A549) Human SMARCD2 1:3~1:4 Negative Online Inquiry
KO13954 SMARCD2 Knockout cell line (HeLa) Human SMARCD2 1:3~1:6 Negative Online Inquiry
KO13955 SMARCD2 Knockout cell line (HCT 116) Human SMARCD2 1:2~1:4 Negative Online Inquiry
KO13956 SMARCD2 Knockout cell line (HEK293) Human SMARCD2 1:3~1:6 Negative Online Inquiry

Background

SMARCD2 Gene Knockout Cell Lines are engineered cellular models featuring targeted deletions of the SMARCD2 gene, a critical component of the SWI/SNF chromatin remodeling complex. These cell lines allow for the exploration of the intricate roles of SMARCD2 in gene expression regulation, cellular differentiation, and various pathophysiological processes, particularly in cancer biology. By employing CRISPR-Cas9 technology, the knockout of the SMARCD2 gene provides researchers with a robust tool to dissect the molecular pathways influenced by chromatin remodeling and to elucidate the gene's contributions to cellular homeostasis.

The primary mechanism of action for these cell lines involves the disruption of the SMARCD2 gene, thereby impairing the function of the SWI/SNF complex. This impairment results in altered chromatin structure and accessibility, leading to modifications in transcriptional activity and gene expression profiles. Consequently, researchers can investigate the roles of SMARCD2 in cellular processes such as proliferation, apoptosis, and response to external stimuli, which are pivotal in understanding diseases, particularly those characterized by aberrant gene regulation.

In research and clinical settings, these SMARCD2 Gene Knockout Cell Lines hold significant scientific importance. They serve as valuable models for studying cancer mechanisms and potential therapeutic targets, providing insights into tumorigenesis and metastasis. Moreover, they are instrumental in the evaluation of novel drug candidates aimed at chromatin remodeling pathways, thereby facilitating the development of precision medicine strategies.

Compared to alternative models, our SMARCD2 Gene Knockout Cell Lines are distinguished by their reliable performance and high-quality genetic validation, ensuring reproducibility and reliability in experimental results. Additionally, they are compatible with a variety of cellular assays, including proliferation, migration, and invasion studies, making them versatile tools for diverse research applications.

For researchers and clinicians focused on cancer biology and chromatin dynamics, these knockout cell lines represent an invaluable resource that can unlock new avenues for discovery. By providing detailed insights into SMARCD2's functions, they empower scientists to drive forward innovative therapeutic strategies.

Our company boasts extensive expertise in developing and producing advanced biological tools, affirming our commitment to enhancing research capabilities and supporting the scientific community with high-quality products that foster groundbreaking discoveries.

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

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