Gene: SMARCA2
Official Full Name: SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2provided by HGNC
Gene Summary: The protein encoded by this gene is a member of the SWI/SNF family of proteins and is highly similar to the brahma protein of Drosophila. Members of this family 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. Alternatively spliced transcript variants encoding different isoforms have been found for this gene, which contains a trinucleotide repeat (CAG) length polymorphism. [provided by RefSeq, Jan 2014]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO00930 | SMARCA2 Knockout cell line(A549) | Human | SMARCA2 | 1:3~1:4 | Negative | Online Inquiry |
KO13964 | SMARCA2 Knockout cell line (HeLa) | Human | SMARCA2 | 1:3~1:6 | Negative | Online Inquiry |
KO13965 | SMARCA2 Knockout cell line (HCT 116) | Human | SMARCA2 | 1:2~1:4 | Negative | Online Inquiry |
KO13966 | SMARCA2 Knockout cell line (HEK293) | Human | SMARCA2 | 1:3~1:6 | Negative | Online Inquiry |
SMARCA2 Gene Knockout Cell Lines are specialized cellular models that have been engineered to lack the expression of the SMARCA2 gene, which encodes a critical member of the SWI/SNF chromatin remodeling complex. By targeting and excising the SMARCA2 gene through advanced CRISPR/Cas9 gene-editing technology, these knockout cell lines serve as an invaluable tool for studying the functional roles of this gene in various biological processes, including chromatin dynamics, gene expression regulation, and cellular differentiation.
The key mechanism by which SMARCA2 knockout cell lines operate involves the disruption of chromatin remodeling activities, which are essential for proper transcriptional regulation. These cell lines allow researchers to investigate how the absence of SMARCA2 influences cellular behavior, responses to stimuli, and the progression of diseases, particularly certain cancers and developmental disorders. In clinical research, they can be employed to identify potential therapeutic targets and unravel molecular pathways associated with SMARCA2-related conditions.
One of the founding advantages of SMARCA2 Gene Knockout Cell Lines is their robust and reproducible nature, providing researchers with a consistent platform for experimentation. Compared to other gene deletion strategies, the CRISPR/Cas9 approach not only offers precise gene editing but also minimizes off-target effects, thereby enhancing the reliability of experimental outcomes. Furthermore, these cell lines can be cultured under standard laboratory conditions, making them accessible for a broad range of studies.
For researchers and clinicians, utilizing SMARCA2 knockout models facilitates cutting-edge investigations into gene function and disease mechanisms, leading to innovative treatment strategies. The insights gained from these studies can lead to advancements in targeted therapies and personalized medicine.
Our company brings extensive expertise in genetic engineering and cellular biology, ensuring that our SMARCA2 Gene Knockout Cell Lines are produced under the highest quality standards. We are committed to supporting the scientific community with reliable and innovative biological products that propel research forward.
Please note that all services are for research use only. Not intended for any clinical use.
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