Home / SLC35F6 Knockout Cell Lines

SLC35F6 Knockout Cell Lines

Gene: SLC35F6

Official Full Name: solute carrier family 35 member F6provided by HGNC

Gene Summary: Predicted to enable transmembrane transporter activity. Involved in negative regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway and positive regulation of cell population proliferation. Located in several cellular components, including lysosomal membrane; mitochondrion; and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2025]

Get A Quote
Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO14014 SLC35F6 Knockout cell line (HeLa) Human SLC35F6 1:3~1:6 Negative Online Inquiry
KO14015 SLC35F6 Knockout cell line (HCT 116) Human SLC35F6 1:2~1:4 Negative Online Inquiry
KO14016 SLC35F6 Knockout cell line (HEK293) Human SLC35F6 1:3~1:6 Negative Online Inquiry
KO14017 SLC35F6 Knockout cell line (A549) Human SLC35F6 1:3~1:4 Negative Online Inquiry

Background

SLC35F6 Gene Knockout Cell Lines are genetically modified cell lines specifically designed to study the functional implications of SLC35F6 gene deletion. These models allow researchers to investigate the role of SLC35F6, which encodes a nucleotide sugar transporter implicated in various cellular processes, including glycosylation pathways and endosomal transport dynamics. By knocking out this gene, scientists can observe alterations in cellular behavior, protein modifications, and overall metabolic functions.

The mechanism of action rests on CRISPR-Cas9 genome editing technology, which precisely introduces breaks in the SLC35F6 gene sequence, resulting in frameshift mutations that effectively disrupt normal gene expression. This precise editing is crucial for elucidating the biological functions of SLC35F6 in health and disease, particularly in contexts such as cancer biology, neurodegenerative disorders, and infectious diseases where glycosylation changes are known to play a significant role.

In research and clinical settings, SLC35F6 Gene Knockout Cell Lines are essential for unraveling the cellular mechanisms by which SLC35F6 influences disease states. Their application in drug discovery and validation processes allows for the identification of novel therapeutic targets and the assessment of potential pharmacological interventions.

The unique selling points of these cell lines include their high specificity, reproducibility, and the ability to provide insights that other less targeted models may not afford. Compared to traditional knockout methods, CRISPR-Cas9 offers a more efficient, cost-effective, and streamlined approach to gene disruption, drastically reducing the time required for generating knockout models.

For researchers and clinicians, the value of SLC35F6 Gene Knockout Cell Lines lies in their ability to accelerate discovery and innovation in understanding disease mechanisms and exploring potential therapeutic avenues. With a robust scientific background and a commitment to quality, our company stands at the forefront of offering cutting-edge biological products, ensuring that researchers have access to the tools necessary for groundbreaking discoveries.

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.