SLC16A2 / MCT8

solute carrier family 16, member 2 (thyroid hormone transporter)

SLC16A2 / MCT8 is 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.

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Proteins (2)

Type

Over-Expression Lysate (2)

Target

SLC16A2 / MCT8 (2)

Publications

No (2)

Tag

Myc-DDK (Flag) (2)

Species

Human (1)

Source

293T Cells (1)

HEK 293 Cells (1)

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SLC16A2 / MCT8 Protein (Over-Expression Lysate Myc-DDK (Flag)) (Full Length) - LS-G115257

Source:

HEK 293 Cells

Tag:

Myc-DDK (Flag)

Molecular Weight:

66.2 kDa

Price:

100 µg/$710

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Human SLC16A2 / MCT8 Protein (Over-Expression Lysate Myc-DDK (Flag)) (Full Length) - LS-G79608

Source:

293T Cells

Tag:

Myc-DDK (Flag)

Molecular Weight:

66.2 kDa

Price:

20 µg/$215

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