Home / SLC12A8 Knockout Cell Lines

SLC12A8 Knockout Cell Lines

Gene: SLC12A8

Official Full Name: solute carrier family 12 member 8provided by HGNC

Gene Summary: This gene is thought to be a candidate for psoriasis susceptibility. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Sep 2010]

Get A Quote
Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO24797 SLC12A8 Knockout cell line (HeLa) Human SLC12A8 1:3~1:6 Negative Online Inquiry
KO24798 SLC12A8 Knockout cell line (HCT 116) Human SLC12A8 1:2~1:4 Negative Online Inquiry
KO24799 SLC12A8 Knockout cell line (A549) Human SLC12A8 1:3~1:4 Negative Online Inquiry

Background

SLC12A8 Gene Knockout Cell Lines are specialized genetically modified cell lines created to lack the SLC12A8 gene, which encodes a sodium-dependent chloride-bicarbonate transporter involved in various physiological processes. These knockout cell lines are pivotal for studying the implications of SLC12A8 in electrolyte balance, neuronal signaling, and muscle function, enabling researchers to dissect the gene's role in both normal and pathological states.

The core function of SLC12A8 is to facilitate the transport of ions across cellular membranes, influencing cellular homeostasis and neurotransmitter release. By employing CRISPR-Cas9 technology or other gene editing methods, our SLC12A8 knockout cell lines provide a unique opportunity to analyze the functional consequences of the absence of this transporter. Researchers can investigate alterations in ion transport, changes in intracellular signaling pathways, and potential compensatory mechanisms that may arise due to SLC12A8 deficiency.

The scientific importance of these cell lines extends to various research applications, including neurobiology, where they can be used to model disorders related to ion transport dysfunction, such as epilepsy or other neurological disorders. In pharmaceutical research, these models can be instrumental for drug screening and understanding drug interactions affecting ionotransport mechanisms.

Unique to our SLC12A8 Gene Knockout Cell Lines is the comprehensive validation and characterization of the knockout status, ensuring researchers have confidence in their experimental results. Furthermore, these cell lines feature robust adaptability for high-throughput screening and can be cultured under standard laboratory conditions, making them user-friendly for both foundational and translational research roles.

For researchers and clinicians seeking reliable models for studying ion transport and its implications in health and disease, our SLC12A8 Gene Knockout Cell Lines present an invaluable resource. With our commitment to quality and innovation in biological products, we empower researchers to accelerate discovery and translate findings into clinical applications effectively.

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

Get a free quote

If your question is not addressed through these resources, you can fill out the online form below and we will answer your question as soon as possible.

0

There is no product in your cart.