Gene: SLC5A11
Official Full Name: solute carrier family 5 member 11provided by HGNC
Gene Summary: Cotransporters, such as SLC5A11, represent a major class of proteins that make use of ion gradients to drive active transport for the cellular accumulation of nutrients, neurotransmitters, osmolytes, and ions Roll et al. (2002) [PubMed 12039040].[supplied by OMIM, Mar 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO30605 | SLC5A11 Knockout cell line (A549) | Human | SLC5A11 | 1:3~1:4 | Negative | Online Inquiry |
SLC5A11 Gene Knockout Cell Lines are meticulously engineered cellular models that have been developed to lack the SLC5A11 gene, which encodes a sodium-dependent glucose transporter (SGLT) involved in glucose uptake and regulation. By utilizing CRISPR-Cas9 gene editing technology, these cell lines provide a precise tool for studying the physiological roles of SLC5A11 and its implications in metabolic disorders. The knockout of this gene disrupts normal glucose transport mechanisms, allowing researchers to investigate how its absence influences cellular metabolism and function under controlled experimental conditions.
The primary function of SLC5A11 is to facilitate the transport of glucose across cell membranes by sodium co-transport. In research settings, these knockout cell lines enable scientists to dissect the pathways affected by SLC5A11, explore its interaction with various metabolic signals, and assess its potential roles in diseases such as diabetes, obesity, and cancer. The loss of this gene aids in elucidating the compensatory mechanisms cells may employ in glucose regulation, thereby advancing our understanding of metabolic homeostasis.
One of the distinct advantages of SLC5A11 Gene Knockout Cell Lines is their specificity and reproducibility, surpassing traditional experimental models that may exhibit variable expression of the target gene. This uniformity allows for more reliable data and conclusions, making them an invaluable resource in both academic and clinical research environments. Additionally, the precision of CRISPR-Cas9 technology enables researchers to confidently attribute observed phenotypic changes specifically to SLC5A11's absence, minimizing confounding factors.
These cell lines are particularly advantageous for researchers and clinicians focusing on metabolic disorders, as they provide a robust platform for drug testing and therapeutic interventions targeting glucose transport mechanisms. By leveraging SLC5A11 Gene Knockout Cell Lines, users can accelerate the discovery of novel treatments and gain insights into glucose-related pathologies.
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Please note that all services are for research use only. Not intended for any clinical use.
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