Gene: PLCG2
Official Full Name: phospholipase C gamma 2provided by HGNC
Gene Summary: The protein encoded by this gene is a transmembrane signaling enzyme that catalyzes the conversion of 1-phosphatidyl-1D-myo-inositol 4,5-bisphosphate to 1D-myo-inositol 1,4,5-trisphosphate (IP3) and diacylglycerol (DAG) using calcium as a cofactor. IP3 and DAG are second messenger molecules important for transmitting signals from growth factor receptors and immune system receptors across the cell membrane. Mutations in this gene have been found in autoinflammation, antibody deficiency, and immune dysregulation syndrome and familial cold autoinflammatory syndrome 3. [provided by RefSeq, Mar 2014]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO11013 | PLCG2 Knockout cell line (HCT 116) | Human | PLCG2 | 1:2~1:4 | Negative | Online Inquiry |
KO11014 | PLCG2 Knockout cell line (HEK293) | Human | PLCG2 | 1:3~1:6 | Negative | Online Inquiry |
KO11015 | PLCG2 Knockout cell line (A549) | Human | PLCG2 | 1:3~1:4 | Negative | Online Inquiry |
PLCG2 Gene Knockout Cell Lines are genetically engineered cells that have had the phospholipase C gamma 2 (PLCG2) gene inactivated to elucidate its biological functions and associated signaling pathways. PLCG2 plays a pivotal role in various cellular processes, including immune cell activation and signaling cascades, primarily in B-lymphocytes and platelets. By producing these knockout cell lines, researchers can investigate the impacts of PLCG2 deficiency on cell proliferation, differentiation, and response to stimuli, which could further our understanding of various immunological diseases and disorders.
The primary mechanism of PLCG2 involves the hydrolysis of phosphatidylinositol 4,5-bisphosphate, leading to the generation of inositol trisphosphate and diacylglycerol, essential second messengers in numerous signaling pathways. The deletion of PLCG2 in these engineered cell lines allows for the observation of altered signaling dynamics and their phenotypic consequences. In a clinical research context, such insights could facilitate the development of targeted therapies for conditions like hyper-IgE syndrome and autoimmune disorders.
Compared to traditional gene editing tools such as CRISPR/Cas9 or shRNA techniques, our PLCG2 Gene Knockout Cell Lines offer a ready-to-use model that saves valuable time and resources, ensuring reproducibility in studies. The knockout cell lines enable researchers to bypass potential complications that arise from incomplete gene editing, providing a clean and defined genetic background to analyze the specific effects of PLCG2 deficiency.
The value of PLCG2 Gene Knockout Cell Lines is further underscored by their applications in drug discovery and the potential to identify novel therapeutic targets for immunological diseases. Researchers and clinicians can rely on this innovative tool to conduct advanced studies with confidence in the reproducibility and validity of their data.
Our company specializes in developing and offering a variety of genetically engineered cell lines and complementary tools for molecular biology research, backed by a deep commitment to advancing scientific progress. The PLCG2 Gene Knockout Cell Lines are part of our extensive product portfolio aimed at enhancing the understanding of critical signaling pathways in health and disease.
Please note that all services are for research use only. Not intended for any clinical use.
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