Home / SLC16A1 Knockout Cell Lines

SLC16A1 Knockout Cell Lines

Gene: SLC16A1

Official Full Name: solute carrier family 16 member 1provided by HGNC

Gene Summary: The protein encoded by this gene is a proton-linked monocarboxylate transporter that catalyzes the movement of many monocarboxylates, such as lactate and pyruvate, across the plasma membrane. Mutations in this gene are associated with erythrocyte lactate transporter defect. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Oct 2009]

Get A Quote
Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO04410 SLC16A1 Knockout cell line (HeLa) Human SLC16A1 1:3~1:6 Negative Online Inquiry
KO04411 SLC16A1 Knockout cell line (HCT 116) Human SLC16A1 1:2~1:4 Negative Online Inquiry
KO04412 SLC16A1 Knockout cell line (HEK293) Human SLC16A1 1:3~1:6 Negative Online Inquiry
KO04413 SLC16A1 Knockout cell line (A549) Human SLC16A1 1:3~1:4 Negative Online Inquiry

Background

SLC16A1 gene knockout cell lines are specialized cellular models designed to facilitate in-depth studies of the SLC16A1 gene, which encodes a member of the monocarboxylate transporter family responsible for the transport of lactate and other small metabolites across cellular membranes. In these knockout models, the SLC16A1 gene has been precisely disrupted, enabling researchers to explore its specific functions, interactions, and implications in metabolic processes more comprehensively.

The primary function of these cell lines lies in their ability to mimic altered metabolic states that have significant implications in various biological contexts, including cancer metabolism and metabolic syndromes. By utilizing these knockout cell lines, researchers can delineate how the absence of SLC16A1 influences lactate transport, cellular energy metabolism, and the overall cellular response under various physiological and pathological conditions. Mechanistically, the disrupted uptake of lactate can affect processes such as the Warburg effect, which is critical in understanding tumorigenesis and cancer progression.

The scientific importance of SLC16A1 knockout cell lines extends into both research and clinical applications. In research, these models serve as invaluable tools for drug discovery, metabolic pathway analysis, and therapeutic target validation, particularly in fields exploring glucose metabolism and hypoxic tumor environments. Clinically, these models may also contribute to the identification of biomarkers for metabolic diseases and offer insights into novel therapeutic strategies.

What sets our SLC16A1 gene knockout cell lines apart from alternatives is our commitment to high-quality genetic editing techniques, ensuring precise and reproducible knockout efficiency. Additionally, our cell lines come with extensive documentation and support, empowering researchers with the necessary data for both preliminary studies and advanced experimental designs.

The value of these cell lines is evident: they provide a foundational tool for unraveling the complexities of cellular metabolism, enabling groundbreaking discoveries in both basic research and clinical translation. Our company is dedicated to advancing scientific knowledge by offering high-quality biological products, underpinned by rigorous research methodologies and expert guidance.

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.