Further Information
AHDS, DXS128, DXS128E, MCT 7, MCT 8, MCT7, MCT8, MRX22, XPCT, monocarboxylate transporter 8, X-linked PEST-containing transporter, monocarboxylate transporter 7, solute carrier family 16, member 2 (thyroid hormone transporter)
WB: 1:500 - 1:2000
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.
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
batch dependent
Unconjugated
Optimal dilutions/concentrations should be determined by the end user. The information provided is a guideline for product use. This product is for research use only.
Recombinant fusion protein containing a sequence corresponding to amino acids 1-100 of human SLC16A2 (NP_006508.2).
6567
solute carrier family 16 member 2
SLC16A2
Homo sapiens
Liquid
PREDICTED MOLECULAR WEIGHT:
Observed: 70kDa
Affinity purification
Cell Cycle, Growth Factors, Neuroscience, Signal Transduction
P36021
Optimal dilutions for each application to be determined by the researcher.