Gene: SMARCC1
Official Full Name: SWI/SNF related BAF chromatin remodeling complex subunit C1provided 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 contains a predicted leucine zipper motif typical of many transcription factors. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO35349 | SMARCC1 Knockout cell line (HeLa) | Human | SMARCC1 | 1:3~1:6 | Negative | Online Inquiry |
KO35350 | SMARCC1 Knockout cell line (HCT 116) | Human | SMARCC1 | 1:2~1:4 | Negative | Online Inquiry |
KO35351 | SMARCC1 Knockout cell line (HEK293) | Human | SMARCC1 | 1:3~1:6 | Negative | Online Inquiry |
KO35352 | SMARCC1 Knockout cell line (A549) | Human | SMARCC1 | 1:3~1:4 | Negative | Online Inquiry |
SMARCC1 Gene Knockout Cell Lines are genetically modified cell cultures specifically designed to lack the SMARCC1 gene, which is a vital component of the SWI/SNF chromatin-remodeling complex. This product serves as an invaluable tool for researchers investigating gene function, chromatin dynamics, and epigenetic regulation. By providing a cellular model devoid of SMARCC1 activity, these knockout cell lines enable the in-depth study of chromatin accessibility, transcriptional regulation, and the downstream effects on cellular pathways involved in development, differentiation, and disease.
The knockout mechanism is facilitated through advanced CRISPR/Cas9 genome-editing technology, which precisely targets the SMARCC1 gene for disruption. The resulting cell lines exhibit altered gene expression patterns and distinct phenotypic changes, making them critical for elucidating the role of SMARCC1 in various biological processes. These cell lines are particularly relevant in cancer research, as dysregulation of chromatin remodeling is a hallmark of many malignancies.
The scientific importance of SMARCC1 Gene Knockout Cell Lines extends into both basic research and clinical applications, providing insight into therapeutic targeting and personalized medicine. Their unique advantages include reproducibility, ease of use in high-throughput screening, and compatibility with various assays, from molecular biology techniques to drug efficacy testing, setting them apart from traditional wild-type cell lines.
Furthermore, these cell lines allow researchers to model diseases associated with chromatin remodeling more accurately, facilitating the exploration of novel therapeutic interventions. The integration of advanced gene-editing techniques ensures high fidelity and specificity in knockout efficiency, making them a superior choice compared to outdated methods.
Our company prides itself on its unparalleled expertise in genetic engineering and cell line development, ensuring that we provide cutting-edge biological products that drive research advancements and clinical breakthroughs. With our SMARCC1 Gene Knockout Cell Lines, both researchers and clinicians can gain a deeper understanding of chromatin dynamics and its implications in health and disease.
Please note that all services are for research use only. Not intended for any clinical use.
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