Home / SLC16A2 Knockout Cell Lines

SLC16A2 Knockout Cell Lines

Gene: SLC16A2

Official Full Name: solute carrier family 16 member 2provided by HGNC

Gene Summary: This gene encodes an integral membrane protein that functions as a transporter of thyroid hormone. The encoded protein facilitates the cellular importation of thyroxine (T4), triiodothyronine (T3), reverse triiodothyronine (rT3) and diidothyronine (T2). This gene is expressed in many tissues and likely plays an important role in the development of the central nervous system. Loss of function mutations in this gene are associated with psychomotor retardation in males while females exhibit no neurological defects and more moderate thyroid-deficient phenotypes. This gene is subject to X-chromosome inactivation. Mutations in this gene are the cause of Allan-Herndon-Dudley syndrome. [provided by RefSeq, Mar 2012]

Get A Quote
Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO35369 SLC16A2 Knockout cell line (HEK293) Human SLC16A2 1:3~1:6 Negative Online Inquiry
KO35370 SLC16A2 Knockout cell line (A549) Human SLC16A2 1:3~1:4 Negative Online Inquiry

Background

SLC16A2 Gene Knockout Cell Lines are a specialized biological product that facilitates the study of the SLC16A2 gene, which encodes the thyroid hormone transporter protein MCT8. These cell lines have been genetically engineered to lack the expression of the SLC16A2 gene, allowing researchers to investigate the physiological and molecular repercussions of its absence. By providing a model in which the regulatory and transport roles of MCT8 can be directly assessed, these knockout cell lines are invaluable for elucidating the underlying mechanisms of thyroid hormone transport and its impact on cellular metabolism.

The specific mechanism of action centers on the disruption of MCT8 expression, which inhibits the uptake of thyroid hormones such as triiodothyronine (T3) and thyroxine (T4). This knockdown can lead to altered metabolic processes, impacting cellular signaling pathways, transcriptional activities, and overall cell functionality. Consequently, these cell lines are essential tools for studying hyperthyroid and hypothyroid conditions, as well as related disorders linked to thyroid hormone metabolism.

In research settings, SLC16A2 Gene Knockout Cell Lines play a crucial role in investigations into thyroid hormone-linked diseases such as Allan-Herndon-Dudley syndrome, providing insights that can lead to potential therapeutic strategies. Clinically, understanding the transport mechanisms mediated by MCT8 can inform the development of drugs that target thyroid hormone signaling pathways, making these cell lines relevant for both basic and translational research.

Compared to conventional models, these knockout cell lines offer distinct advantages by providing a “clean” system devoid of confounding factors, enabling precise experimentation with defined variables. Researchers benefit from high reproducibility of results, as well as enhanced accuracy and control in experimental design.

For researchers and clinicians focused on thyroid-related studies, the SLC16A2 Gene Knockout Cell Lines represent a critical asset for advancing scientific knowledge and potential clinical applications. Our company, specialized in the development of high-quality biological products, is committed to supporting your research endeavors with precision-engineered tools that facilitate groundbreaking discoveries in gene expression and protein function.

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.