Gene: SERINC3
Official Full Name: serine incorporator 3provided by HGNC
Gene Summary: Predicted to enable L-serine transmembrane transporter activity. Involved in defense response to virus; detection of virus; and innate immune response. Predicted to be located in plasma membrane. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Apr 2025]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO31378 | SERINC3 Knockout cell line (HeLa) | Human | SERINC3 | 1:3~1:6 | Negative | Online Inquiry |
KO31379 | SERINC3 Knockout cell line (HCT 116) | Human | SERINC3 | 1:2~1:4 | Negative | Online Inquiry |
KO31380 | SERINC3 Knockout cell line (HEK293) | Human | SERINC3 | 1:3~1:6 | Negative | Online Inquiry |
KO31381 | SERINC3 Knockout cell line (A549) | Human | SERINC3 | 1:3~1:4 | Negative | Online Inquiry |
SERINC3 Gene Knockout Cell Lines are specially engineered cellular systems designed to study the function and role of the SERINC3 gene, which encodes a protein involved in the modulation of viral entry into host cells. These knockout cell lines are created through CRISPR/Cas9 technology, which allows for precise genome editing, resulting in a significant deletion of the SERINC3 gene. This precise modification enables researchers to investigate how the absence of SERINC3 affects various biological pathways, particularly those related to viral pathogenesis, immune responses, and cellular signaling.
The key function of SERINC3 is its involvement in hindering the entry of several enveloped viruses, including HIV-1 and other retroviruses, into host cells. By utilizing the SERINC3 knockout model, researchers can elucidate the molecular mechanisms of viral evasion strategies and assess the impact of SERINC3 absence on viral infectivity and replication. This resultant understanding is crucial for the development of novel antiviral therapies and vaccines, highlighting its importance in both basic and applied research settings.
What sets SERINC3 Gene Knockout Cell Lines apart from competing products is their high specificity and reliability. Unlike traditional RNA interference methods that provide transient knockdown, the CRISPR/Cas9 gene knockout offers a permanent alteration in the cell line, ensuring consistent study conditions over time. This permanence facilitates reproducibility in experimental outcomes and allows for long-term studies of cellular responses without the variability introduced by transient methods.
The SERINC3 Gene Knockout Cell Lines represent a valuable resource for researchers and clinicians focusing on virology, immunology, and gene function. They empower scientists to uncover critical insights into viral-host interactions and bolster the quest for innovative treatments against viral infections.
Our company, known for its commitment to advancing scientific research, specializes in providing high-quality biological products tailored for the needs of the scientific community. With extensive experience in cell line engineering and a robust quality control framework, we ensure that our products meet rigorous standards for reliability and performance, making us a trusted partner in cutting-edge research initiatives.
Please note that all services are for research use only. Not intended for any clinical use.
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