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SNX4 Knockout Cell Lines

Gene: SNX4

Official Full Name: sorting nexin 4provided by HGNC

Gene Summary: This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein associated with the long isoform of the leptin receptor and with receptor tyrosine kinases for platelet-derived growth factor, insulin, and epidermal growth factor in cell cultures, but its function is unknown. This protein may form oligomeric complexes with family members. Two transcript variants, one protein coding and the other non-protein coding, have been found for this gene. [provided by RefSeq, Nov 2012]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO33920 SNX4 Knockout cell line (HeLa) Human SNX4 1:3~1:6 Negative Online Inquiry
KO33921 SNX4 Knockout cell line (HCT 116) Human SNX4 1:2~1:4 Negative Online Inquiry
KO33922 SNX4 Knockout cell line (HEK293) Human SNX4 1:3~1:6 Negative Online Inquiry
KO33923 SNX4 Knockout cell line (A549) Human SNX4 1:3~1:4 Negative Online Inquiry

Background

SNX4 Gene Knockout Cell Lines are precisely engineered cellular models that facilitate the study of the sorting nexin 4 (SNX4) gene's role in cellular processes. These cell lines are generated through the application of CRISPR-Cas9 gene-editing technology, which introduces targeted mutations into the SNX4 gene, effectively disrupting its function. By providing a loss-of-function model, these knockout cell lines enable researchers to elucidate the biological significance of SNX4 in various cellular pathways, including endocytosis and autophagy.

The primary function of SNX4 involves its interaction with phosphoinositides and its role in vesicle trafficking within the cell. The absence of SNX4 as seen in these knockout lines can significantly alter intracellular signaling and protein sorting mechanisms, making them an invaluable tool for understanding diseases associated with aberrant trafficking and organelle dysfunction.

Scientifically, these cell lines are of paramount importance in drug discovery, disease modeling, and molecular biology research. Their application spans various domains, including cancer research, neurobiology, and metabolic disorders, allowing researchers to investigate the pathophysiological implications of SNX4 dysregulation in specific conditions and explore potential therapeutic strategies.

One of the key advantages of our SNX4 Gene Knockout Cell Lines is the precise and reliable nature of gene editing, ensuring reproducibility and consistency across experiments. Unlike other methods such as RNA interference, which can only reduce gene function, complete knockout allows for definitive conclusions regarding gene function. Furthermore, our cell lines are rigorously validated for their genetic edits and characterized to ensure they maintain normal cellular physiology.

For researchers and clinicians focused on the mechanistic understanding of cellular processes or the development of targeted interventions, the SNX4 Gene Knockout Cell Lines offer a powerful resource to accelerate discovery and innovation. Our company prides itself on its expertise in developing advanced genetic models and is committed to equipping scientific communities with high-quality products tailored for meaningful research outcomes.

Please note that all services are for research use only. Not intended for any clinical use.

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