Gene: SMARCAL1
Official Full Name: SNF2 related chromatin remodeling annealing helicase 1provided by HGNC
Gene Summary: The protein encoded by this gene is a member of the SWI/SNF family of proteins. 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 shows sequence similarity to the E. coli RNA polymerase-binding protein HepA. Mutations in this gene are a cause of Schimke immunoosseous dysplasia (SIOD), an autosomal recessive disorder with the diagnostic features of spondyloepiphyseal dysplasia, renal dysfunction, and T-cell immunodeficiency. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO06883 | SMARCAL1 Knockout cell line (HeLa) | Human | SMARCAL1 | 1:3~1:6 | Negative | Online Inquiry |
KO06884 | SMARCAL1 Knockout cell line (HCT 116) | Human | SMARCAL1 | 1:2~1:4 | Negative | Online Inquiry |
KO06885 | SMARCAL1 Knockout cell line (HEK293) | Human | SMARCAL1 | 1:3~1:6 | Negative | Online Inquiry |
KO06886 | SMARCAL1 Knockout cell line (A549) | Human | SMARCAL1 | 1:3~1:4 | Negative | Online Inquiry |
SMARCAL1 Gene Knockout Cell Lines are specialized cellular models engineered to disrupt the SMARCAL1 gene, which encodes a key protein involved in the maintenance of genome integrity. The disruption of this gene enables the study of DNA repair mechanisms and the cellular stress responses elicited by DNA damage, offering insights into various biological processes and disease states.
These cell lines function by employing CRISPR-Cas9 gene editing technology to create precise deletions or mutations within the SMARCAL1 gene, effectively abolishing its protein expression. This knockout model mimics the genetic conditions found in certain pathologies, providing a robust in vitro platform for investigating the roles of SMARCAL1 in DNA damage response and repair signaling pathways. Researchers can utilize these cell lines to assess cellular proliferation, apoptosis, and mutation frequencies, yielding critical data relevant to cancer biology, neurodegenerative diseases, and developmental disorders.
The scientific importance of SMARCAL1 Gene Knockout Cell Lines extends to both fundamental research and clinical applications. They are indispensable in drug discovery and molecular biology studies, offering a controlled environment to test hypothesized interactions with therapeutic agents. Furthermore, the functional characterization of SMARCAL1 through these knockout models helps elucidate its role in tumorigenesis, making them valuable assets in oncology research.
Compared to other genetic manipulation tools, these knockout cell lines stand out due to their high efficiency, specificity, and reproducibility. Researchers benefit from the clear phenotypic outcomes associated with SMARCAL1 disruption, allowing for straightforward interpretation of experimental results. This clarity provides a significant advantage when validating findings or exploring novel therapeutic strategies.
In summary, SMARCAL1 Gene Knockout Cell Lines offer unparalleled value to researchers and clinicians alike, facilitating advanced studies of genetic regulation and cellular responses to DNA damage. Our company is committed to empowering scientific excellence, providing high-quality biological products designed to support your research initiatives and drive innovation in the life sciences.
Please note that all services are for research use only. Not intended for any clinical use.
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