Home / SLC16A3 Knockout Cell Lines

SLC16A3 Knockout Cell Lines

Gene: SLC16A3

Official Full Name: solute carrier family 16 member 3provided by HGNC

Gene Summary: Lactic acid and pyruvate transport across plasma membranes is catalyzed by members of the proton-linked monocarboxylate transporter (MCT) family, which has been designated solute carrier family-16. Each MCT appears to have slightly different substrate and inhibitor specificities and transport kinetics, which are related to the metabolic requirements of the tissues in which it is found. The MCTs, which include MCT1 (SLC16A1; MIM 600682) and MCT2 (SLC16A7; MIM 603654), are characterized by 12 predicted transmembrane domains (Price et al., 1998 [PubMed 9425115]).[supplied by OMIM, Mar 2008]

Get A Quote
Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO06821 SLC16A3 Knockout cell line (HeLa) Human SLC16A3 1:3~1:6 Negative Online Inquiry
KO06822 SLC16A3 Knockout cell line (HCT 116) Human SLC16A3 1:2~1:4 Negative Online Inquiry
KO06823 SLC16A3 Knockout cell line (HEK293) Human SLC16A3 1:3~1:6 Negative Online Inquiry
KO06824 SLC16A3 Knockout cell line (A549) Human SLC16A3 1:3~1:4 Negative Online Inquiry

Background

SLC16A3 Gene Knockout Cell Lines comprise engineered cellular models in which the SLC16A3 gene, encoding the monocarboxylate transporter 1 (MCT1), has been selectively disrupted. These cell lines serve as invaluable tools for studying the physiological role of MCT1 in various biological processes, such as metabolic pathways, cellular respiration, and acid-base homeostasis. By ablating the SLC16A3 gene, researchers can observe the resultant phenotypic changes, allowing for a clearer understanding of the transport mechanisms that influence lactate and pyruvate dynamics in both normal and pathological states.

The primary function of SLC16A3 gene knockout cell lines lies in their ability to enable detailed investigation into the functional implications of MCT1 deficiency. This includes exploring alterations in cellular metabolism and examining how different cancer cell lines utilize the lactate shuttle for energy production. The mechanistic insights gleaned from these models are instrumental in elucidating MCT1's role in tumor biology, neurodegenerative diseases, and sports medicine, where lactate metabolism is critical.

Scientifically, these cell lines hold significant importance in both research and clinical applications. They are particularly relevant in therapeutic research targeting metabolic diseases and cancer, where the modulation of monocarboxylate transport can impact tumor growth and survival. These models facilitate the screening of novel compounds aimed at modulating MCT1 activity, potentially leading to breakthrough treatments.

Compared to traditional cell lines, SLC16A3 gene knockout cell lines provide a unique advantage by enabling specific study of MCT1's functions without the confounding factors of its normal expression. This specificity not only enhances the reliability of experimental outcomes but also provides a more accurate representation of pathophysiological conditions in vivo.

For researchers and clinicians focused on metabolic regulation and cancer research, employing SLC16A3 gene knockout cell lines presents an opportunity to unlock new avenues for discovery. At our company, we specialize in developing next-generation cellular models tailored for cutting-edge research, ensuring that our products are of the highest quality and rigorously characterized to meet the needs of the scientific community.

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.