Gene: RASA1
Official Full Name: RAS p21 protein activator 1provided by HGNC
Gene Summary: The protein encoded by this gene is located in the cytoplasm and is part of the GAP1 family of GTPase-activating proteins. The gene product stimulates the GTPase activity of normal RAS p21 but not its oncogenic counterpart. Acting as a suppressor of RAS function, the protein enhances the weak intrinsic GTPase activity of RAS proteins resulting in the inactive GDP-bound form of RAS, thereby allowing control of cellular proliferation and differentiation. Mutations leading to changes in the binding sites of either protein are associated with basal cell carcinomas. Mutations also have been associated with hereditary capillary malformations (CM) with or without arteriovenous malformations (AVM) and Parkes Weber syndrome. Alternative splicing results in two isoforms where the shorter isoform, lacking the N-terminal hydrophobic region but retaining the same activity, appears to be abundantly expressed in placental but not adult tissues. [provided by RefSeq, May 2012]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO10521 | RASA1 Knockout cell line (HeLa) | Human | RASA1 | 1:3~1:6 | Negative | Online Inquiry |
KO10522 | RASA1 Knockout cell line (HCT 116) | Human | RASA1 | 1:2~1:4 | Negative | Online Inquiry |
KO10523 | RASA1 Knockout cell line (HEK293) | Human | RASA1 | 1:3~1:6 | Negative | Online Inquiry |
KO10524 | RASA1 Knockout cell line (A549) | Human | RASA1 | 1:3~1:4 | Negative | Online Inquiry |
RASA1 Gene Knockout Cell Lines are genetically modified cell lines in which the RASA1 gene has been disrupted or deleted, providing invaluable tools for the study of cellular signaling pathways and their associated functions. RASA1 encodes a critical regulator of RAS signaling, acting as a negative regulator of the RAS-RAF-MAPK pathway that is often aberrantly activated in various cancers. The knockout of this gene allows researchers to investigate the role of RASA1 in cellular differentiation, proliferation, and apoptosis, adding significant insight into tumorigenesis and potential therapeutic targets.
The primary mechanism of action for these cell lines relies on the loss of RASA1’s regulatory effects on RAS signaling. By studying the resultant phenotypic changes, scientists can elucidate how the dysregulation of this signaling pathway influences cancer progression and response to treatment. These cell lines are especially useful in screening for drug resistance and in assessing the efficacy of novel therapeutics aimed at targeting RAS-driven cancers.
The scientific significance of RASA1 Gene Knockout Cell Lines extends beyond oncology; they also serve as models for neurodevelopmental disorders and other pathologies where RAS signaling plays a crucial role. In clinical and research settings, these cell lines provide a consistent and reproducible platform for experimentation, offering an advantage over primary cell cultures that may present variability and complexity.
One of the unique selling points of our RASA1 Gene Knockout Cell Lines is their validated background involving state-of-the-art CRISPR/Cas9 gene editing technology, ensuring precise gene disruption. This precision translates into reliable experimental outcomes and a minimized risk of off-target effects compared to traditional knockout techniques. Furthermore, the ability to obtain these cell lines in various backgrounds or with additional markers facilitates tailored experimental designs.
For researchers and clinicians looking to deepen their understanding of RAS-related signal transduction, these cell lines are an essential asset due to their ability to mimic in vivo conditions while providing clear and interpretable data. Our company is committed to advancing biological research by offering high-quality, well-characterized genetic models that enable innovative discoveries and enhance therapeutic development.
Please note that all services are for research use only. Not intended for any clinical use.
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