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SLC16A2/MCT8 Proteins

(Solute Carrier Family 16 Member 2 (SLC16A2))

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].

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SLC16A2/MCT8 Protein (ABIN1330488)

SLC16A2 Origin: Human Host: Wheat germ Recombinant AP

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SLC16A2/MCT8 Proteins by Origin

Find SLC16A2/MCT8 Proteins for a variety of species such as anti-Human SLC16A2/MCT8. The species listed below are among those available. Click on a link to go to the corresponding products.

SLC16A2/MCT8 Proteins by Source

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SLC16A2/MCT8 Proteins by Protein Type

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SLC16A2/MCT8 Proteins by Application

Find SLC16A2/MCT8 Proteins validated for a specific application such as AP. Some of the available applications are listed below. Click on a link to go to the corresponding products.

Popular SLC16A2/MCT8 Proteins

Product

Reactivity

Source

Validations

Cat. No.

Quantity

Datasheet

SLC16A2/MCT8 Protein

Reactivity Human

Source Wheat germ

Validations

Cat. No. ABIN1330488

Quantity 10 μg

Datasheet Datasheet

Aliases for SLC16A2/MCT8 Proteins

solute carrier family 16 member 2 (SLC16A2) Proteins
solute carrier family 16 (monocarboxylic acid transporters), member 2 (Slc16a2) Proteins
solute carrier family 16 member 2 (Slc16a2) Proteins
AHDS Proteins
AW105741 Proteins
DXS128 Proteins
DXS128E Proteins
MCT 7 Proteins
MCT7 Proteins
MCT8 Proteins
Mct8 Proteins
MCT 8 Proteins
MRX22 Proteins
Xpct Proteins
XPCT Proteins

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