Gene: SIPA1L2
Official Full Name: signal induced proliferation associated 1 like 2provided by HGNC
Gene Summary: This gene encodes a member of the signal-induced proliferation-associated 1 like family. Members of this family contain a GTPase activating domain, a PDZ domain and a C-terminal coiled-coil domain with a leucine zipper. A similar protein in rat acts as a GTPases for the small GTPase Rap. [provided by RefSeq, Sep 2015]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO08728 | SIPA1L2 Knockout cell line (HeLa) | Human | SIPA1L2 | 1:3~1:6 | Negative | Online Inquiry |
KO08729 | SIPA1L2 Knockout cell line (HCT 116) | Human | SIPA1L2 | 1:2~1:4 | Negative | Online Inquiry |
KO08730 | SIPA1L2 Knockout cell line (HEK293) | Human | SIPA1L2 | 1:3~1:6 | Negative | Online Inquiry |
KO08731 | SIPA1L2 Knockout cell line (A549) | Human | SIPA1L2 | 1:3~1:4 | Negative | Online Inquiry |
SIPA1L2 Gene Knockout Cell Lines are genetically modified cellular models designed to investigate the function and implications of the SIPA1L2 gene in various biological processes. SIPA1L2 (Signal-Induced Proliferation Associated 1 Like 2) encodes a protein involved in regulating cellular signaling pathways, particularly those related to cell proliferation, migration, and survival. Using CRISPR-Cas9 technology, these cell lines have been created to disable the SIPA1L2 gene, allowing researchers to explore its role in oncogenesis, signal transduction, and cellular response mechanisms in both normal and pathological states.
The primary function of the SIPA1L2 Gene Knockout Cell Lines is to provide a powerful tool for elucidating the functional aspects of the SIPA1L2 protein. Researchers can utilize these cell lines to conduct loss-of-function studies, which can reveal how the absence of SIPA1L2 affects cellular behaviors such as growth patterns, apoptotic responses, and molecular signaling pathways. The manipulation of gene expression in these cell lines facilitates the assessment of SIPA1L2's contribution to diseases, especially in the realms of cancer research and neurobiology.
The scientific importance of these cell lines lies in their potential applications across diverse research domains. They can significantly advance our understanding of cancer biology by revealing the role of SIPA1L2 in tumor progression and metastasis, opening avenues for targeted therapies. Furthermore, these knockout models can be pivotal for drug discovery and screening, enabling the evaluation of therapeutic compounds that may interact with the pathways influenced by SIPA1L2.
Compared to traditional cell lines that express the SIPA1L2 gene, these knockout cell lines offer unique advantages such as precision in investigating gene-specific roles and reduced variability associated with genetic background. Researchers can confidently explore the output of SIPA1L2 disruption, leading to more robust and reproducible data than what may be achievable with other methods such as pharmacological inhibition or RNA interference.
For researchers and clinicians seeking to deepen their understanding of various diseases and explore novel therapeutic approaches, the SIPA1L2 Gene Knockout Cell Lines represent an invaluable resource. They embody a significant step forward in precision research, offering insights that can inform both basic and translational science.
Our company is committed to advancing scientific research by providing high-quality, innovative tools such as the SIPA1L2 Gene Knockout Cell Lines, backed by a team of experts in genetic engineering and molecular biology dedicated to supporting the scientific community's needs.
Please note that all services are for research use only. Not intended for any clinical use.
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