Gene: ARID1A
Official Full Name: AT-rich interaction domain 1Aprovided by HGNC
Gene Summary: This gene encodes a member of the SWI/SNF family, whose members have helicase and ATPase activities and 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, which is required for transcriptional activation of genes normally repressed by chromatin. It possesses at least two conserved domains that could be important for its function. First, it has a DNA-binding domain that can specifically bind an AT-rich DNA sequence known to be recognized by a SNF/SWI complex at the beta-globin locus. Second, the C-terminus of the protein can stimulate glucocorticoid receptor-dependent transcriptional activation. It is thought that the protein encoded by this gene confers specificity to the SNF/SWI complex and may recruit the complex to its targets through either protein-DNA or protein-protein interactions. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
GP00483 | ARID1A gRNA3-gRNA4 KO plasmid | ARID1A | $850 | |||
KO00640 | ARID1A Knockout cell line(NCI-H1299) | Human | ARID1A | 1:2~1:3 | Negative | Online Inquiry |
KO00665 | ARID1A Knockout cell line(A549) | Human | ARID1A | 1:3~1:4 | Negative | Online Inquiry |
KO09395 | ARID1A Knockout cell line (HeLa) | Human | ARID1A | 1:3~1:6 | Negative | Online Inquiry |
KO09396 | ARID1A Knockout cell line (HCT 116) | Human | ARID1A | 1:2~1:4 | Negative | Online Inquiry |
KO09397 | ARID1A Knockout cell line (HEK293) | Human | ARID1A | 1:3~1:6 | Negative | Online Inquiry |
ARID1A Gene Knockout Cell Lines are specifically engineered cellular models that facilitate the study of the ARID1A gene's function by effectively inactivating its expression. The ARID1A (AT-rich interaction domain 1A) gene is crucial for chromatin remodeling and plays a significant role in various cellular processes, including transcription regulation and DNA repair. By utilizing CRISPR-Cas9 technology, these cell lines offer a robust methodology to analyze the functional consequences of ARID1A loss on cellular physiology, gene expression patterns, and metabolic pathways.
The key mechanism behind these knockout cell lines lies in the precise introduction of targeted mutations within the ARID1A gene, resulting in the disruption of its protein coding sequence. This results in a loss of ARID1A function, thereby allowing researchers to investigate phenotype alterations that occur as a result of this genetic modification. Such investigations are invaluable for understanding the role of ARID1A in cancer biology, particularly as mutations in ARID1A have been implicated in various tumor types, including ovarian and endometrial cancers.
The scientific importance of ARID1A Gene Knockout Cell Lines is evident in both research and clinical settings. These cell lines provide a vital tool for drug discovery, enabling researchers to test the efficacy of novel therapeutic agents targeting ARID1A-deficient tumors. Additionally, they serve as a platform for investigating the molecular mechanisms driving tumorigenesis and resistance to therapies, allowing for the development of customized treatment strategies.
Compared to alternative products, such as traditional RNA interference methods, the CRISPR-based ARID1A knockout models offer greater precision, efficiency, and permanence in gene disruption. This specificity not only enhances the reliability of experimental outcomes but also provides researchers with a clearer understanding of ARID1A's functional role without the variability associated with knockdown strategies.
For researchers and clinicians aiming to deepen their understanding of the implications of ARID1A loss, these knockout cell lines represent a powerful resource. By harnessing state-of-the-art engineering techniques, our company is committed to supplying high-quality biological products that meet the demands of cutting-edge research, supporting scientific innovation and advancing the fields of genetics and oncology. Our expertise in gene editing and cell line development ensures that users receive a product that is not only reliable but also instrumental in driving their research forward.
Please note that all services are for research use only. Not intended for any clinical use.
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