Tissue expression
Cell line expression
Protein structure

SLC16A2

Solute carrier family 16 member 2
AHDS, DXS128, MCT7, MCT8, MRX22, XPCT 
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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199 antibodies from 30 providers.

Antibody properties

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AntibodyRefsTypeWBELICCIPIHCFC
Atlas Antibodies
2 antibodies
Proteintech Group
1 antibody
Novus Biologicals
4 antibodies
OriGene
2 antibodies
Invitrogen Antibodies
12 antibodies
antibodies-online
66 antibodies
Biorbyt
24 antibodies
NovoPro Bioscience Inc.
2 antibodies
Acris Antibodies GmbH
1 antibody
Affinity Biosciences
1 antibody
Cusabio Biotech Co., Ltd
3 antibodies
Bethyl Laboratories
1 antibody
FineTest Biotech
1 antibody
St John's Laboratory
2 antibodies
Aviva Systems Biology
1 antibody
GeneTex
2 antibodies
Bioworld Technology, Inc
1 antibody
MilliporeSigma / Merck KGaA
3 antibodies
Abnova Corporation
2 antibodies
Boster Biological Technology
1 antibody
Abbexa
4 antibodies
Abbkine Scientific Co.Ltd.
1 antibody
Abgent
1 antibody
EMD Millipore
1 antibody
Leading Biology
1 antibody
United States Biological
24 antibodies
MyBioSource
3 antibodies
Creative Diagnostics
1 antibody