Gene: SLC39A4
Official Full Name: solute carrier family 39 member 4provided by HGNC
Gene Summary: This gene encodes a member of the zinc/iron-regulated transporter-like protein (ZIP) family. The encoded protein localizes to cell membranes and is required for zinc uptake in the intestine. Mutations in this gene result in acrodermatitis enteropathica. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2013]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO14003 | SLC39A4 Knockout cell line (HeLa) | Human | SLC39A4 | 1:3~1:6 | Negative | Online Inquiry |
KO14004 | SLC39A4 Knockout cell line (HCT 116) | Human | SLC39A4 | 1:2~1:4 | Negative | Online Inquiry |
KO14005 | SLC39A4 Knockout cell line (HEK293) | Human | SLC39A4 | 1:3~1:6 | Negative | Online Inquiry |
KO14006 | SLC39A4 Knockout cell line (A549) | Human | SLC39A4 | 1:3~1:4 | Negative | Online Inquiry |
SLC39A4 Gene Knockout Cell Lines are specialized cellular models engineered for the targeted disruption of the SLC39A4 gene, which encodes the zinc transporter ZIP4. This gene is critically involved in zinc homeostasis and plays a vital role in various physiological processes, including cellular metabolism, immune response, and growth regulation. By utilizing CRISPR-Cas9 technology, these knockout cell lines facilitate the precise modification of the gene, allowing researchers to explore the consequences of zinc deficiency and the cellular mechanisms underpinning zinc-related disorders.
The primary function of SLC39A4 Gene Knockout Cell Lines lies in their ability to mimic pathological conditions associated with disrupted zinc transport, enabling a more profound understanding of diseases such as acrodermatitis enteropathica and certain cancers. These cell lines serve as invaluable tools for investigating the functional role of ZIP4 in cellular signaling pathways, including those related to apoptosis, oxidative stress, and inflammation. Moreover, they allow for the elucidation of therapeutic targets for diseases stemming from zinc deficiencies or dysregulation.
In the scientific community, these cell lines hold significant importance for both basic and applied research. Their application ranges from studying gene function and metabolic pathways to testing new pharmacological agents that may target zinc transport mechanisms. By comparing SLC39A4 knockout cells to wild-type counterparts, researchers can measure variations in cellular behavior and examine the potential for therapeutic intervention.
One of the key advantages of SLC39A4 Gene Knockout Cell Lines is their specificity; they provide a clean genetic background for studying the direct impacts of gene disruption without confounding effects from normal gene expression. Unlike other models that may exhibit variable expression of target genes, these knockout lines offer a more consistent and reliable platform for experimentation, facilitating reproducibility across studies.
For researchers and clinicians focused on metabolic diseases, cancer biology, or nutrition, the SLC39A4 Gene Knockout Cell Lines present an unparalleled opportunity to advance the underlying knowledge of zinc transport and its implications for health. By incorporating this innovative tool into their research arsenal, they can unlock new insights and contribute significantly to the field of molecular biology.
Our company specializes in developing high-quality, genetically engineered cell lines, and we are committed to supporting cutting-edge research with precision tools that empower scientists in their quest to understand complex biological systems.
Please note that all services are for research use only. Not intended for any clinical use.
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