Gene: ESYT2
Official Full Name: extended synaptotagmin 2provided by HGNC
Gene Summary: Enables calcium ion binding activity; identical protein binding activity; and phospholipid binding activity. Predicted to be involved in endocytosis; endoplasmic reticulum-plasma membrane tethering; and lipid transport. Located in several cellular components, including cytoplasmic side of plasma membrane; endoplasmic reticulum membrane; and endoplasmic reticulum-plasma membrane contact site. [provided by Alliance of Genome Resources, Apr 2025]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO17879 | ESYT2 Knockout cell line (HeLa) | Human | ESYT2 | 1:3~1:6 | Negative | Online Inquiry |
KO17880 | ESYT2 Knockout cell line (HCT 116) | Human | ESYT2 | 1:2~1:4 | Negative | Online Inquiry |
KO17881 | ESYT2 Knockout cell line (HEK293) | Human | ESYT2 | 1:3~1:6 | Negative | Online Inquiry |
KO17882 | ESYT2 Knockout cell line (A549) | Human | ESYT2 | 1:3~1:4 | Negative | Online Inquiry |
The ESYT2 Gene Knockout Cell Lines are specialized cellular models generated through the precise deletion of the ESYT2 gene, which encodes for extended synaptotagmin-2, a protein critical in the regulation of membrane dynamics and lipid transport within cellular systems. These knockout (KO) cell lines serve as invaluable tools for researchers investigating the physiological and pathological roles of ESYT2 in a variety of biological processes, particularly those related to neuronal function and membrane trafficking.
The key function of the ESYT2 KO cell lines lies in their ability to mimic conditions of ESYT2 deficiency, allowing for the elucidation of the gene's contribution to cellular pathways. The deletion of ESYT2 significantly impacts lipid biogenesis and synaptic transmission, offering insights into how its dysregulation may contribute to neurodegenerative diseases or synaptic disorders. These cell lines provide a robust platform for functional studies, high-throughput screening, and drug discovery efforts.
Scientifically, the ESYT2 Gene Knockout Cell Lines are crucial for advancing our understanding of cellular mechanisms underpinning neurological function and disease. They can be employed in academic research focusing on synaptic plasticity, lipid metabolism, and cellular communication. Additionally, these models can play a role in translational research, potentially guiding the development of therapeutic strategies targeting ESYT2-related disorders.
What sets these knockout cell lines apart from conventional models is their precision and specificity, which allow researchers to study the absence of ESYT2 in controlled environments. This level of specificity enhances data integrity and reproducibility compared to heterogeneous systems or pharmacological inhibitors. Moreover, with growing recognition of lipid-protein interactions in various cellular functions, the ESYT2 KO cell lines represent a timely addition to the researcher’s toolkit.
For scientists and clinicians alike, these cell lines offer substantial value in dissecting the molecular mechanisms of diseases linked to ESYT2, paving the way for innovative approaches to treatment and intervention. Our company’s commitment to providing high-quality biological models is reaffirmed through our expertise in gene-editing technologies and our extensive portfolio of cell line products, ensuring that researchers can conduct their work with confidence and efficacy.
Please note that all services are for research use only. Not intended for any clinical use.
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