Gene: CAST
Official Full Name: calpastatinprovided by HGNC
Gene Summary: The protein encoded by this gene is an endogenous calpain (calcium-dependent cysteine protease) inhibitor. It consists of an N-terminal domain L and four repetitive calpain-inhibition domains (domains 1-4), and it is involved in the proteolysis of amyloid precursor protein. The calpain/calpastatin system is involved in numerous membrane fusion events, such as neural vesicle exocytosis and platelet and red-cell aggregation. The encoded protein is also thought to affect the expression levels of genes encoding structural or regulatory proteins. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jun 2010]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO06310 | CAST Knockout cell line (HeLa) | Human | CAST | 1:3~1:6 | Negative | Online Inquiry |
KO06311 | CAST Knockout cell line (HCT 116) | Human | CAST | 1:2~1:4 | Negative | Online Inquiry |
KO06312 | CAST Knockout cell line (HEK293) | Human | CAST | 1:3~1:6 | Negative | Online Inquiry |
KO06313 | CAST Knockout cell line (A549) | Human | CAST | 1:3~1:4 | Negative | Online Inquiry |
CAST Gene Knockout Cell Lines are precision-engineered cellular models designed to facilitate the study of gene function through targeted gene disruption. These cell lines are developed using advanced CRISPR/Cas9 technology, enabling researchers to create specific knockout mutations in the gene of interest. By eliminating the expression of proteins produced by these targeted genes, CAST Gene Knockout Cell Lines allow for the direct examination of the resultant phenotypic changes, biochemical pathways, and cellular behaviors associated with gene loss.
The key mechanisms behind these cell lines involve the use of guide RNAs (gRNAs) that direct the CRISPR-associated protein, Cas9, to a specific DNA sequence. This leads to double-strand breaks in the genomic DNA, which, when repaired through non-homologous end joining, result in insertion or deletion mutations that effectively disrupt gene function. This targeted approach not only enhances precision but also reduces off-target effects commonly associated with less specific gene editing methods.
Scientifically, CAST Gene Knockout Cell Lines hold immense importance in various research and clinical applications, ranging from basic biological research to therapeutic development. They provide unparalleled insights into gene function, disease mechanisms, and therapeutic targets, making them invaluable for studies focused on cancer biology, genetic disorders, and drug discovery. In clinical settings, these cell lines can be utilized for preclinical testing of therapeutic interventions, aiding in the rapid identification of potential treatment strategies.
Compared to alternative models, CAST Gene Knockout Cell Lines offer distinct advantages, including high efficiency, reproducibility, and the ability to utilize a wide array of cell types. Their contributions to the advancement of gene editing technologies and the elucidation of genetic roles in health and disease underscore their unique selling points, making them the preferred choice for discerning researchers and clinicians.
For those engaged in cutting-edge biomedical research or clinical investigations, CAST Gene Knockout Cell Lines represent a transformative tool that can significantly enhance experimental outcomes. With a commitment to scientific excellence and innovation, our company stands at the forefront of supplying advanced biological products tailored to meet the evolving needs of researchers and healthcare professionals.
Please note that all services are for research use only. Not intended for any clinical use.
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