Solute Carrier Family 16 Member 2 (SLC16A2) Antibody

SLC16A2 Antibody is a Rabbit Polyclonal antibody against 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.

Target	Solute Carrier Family 16 Member 2 (SLC16A2)
Clonality	Polyclonal
Reactivity	Human, Mouse, Rat
Tested Applications	WB
Host	Rabbit
Recommended dilutions	WB: 1/500 - 1/2000. Optimal dilutions/concentrations should be determined by the end user.
Conjugation	Unconjugated
Immunogen	Recombinant fusion protein containing a sequence corresponding to amino acids 1-100 of human SLC16A2.
Isotype	IgG
Form	Liquid
Purification	Purified by affinity chromatography.
Storage	Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
UniProt Primary AC	P36021 (UniProt, ExPASy)
UniProt Secondary AC	Q7Z797
UniProt Entry Name	MOT8_HUMAN
Gene Symbol	SLC16A2
GeneID	6567
NCBI Accession	NP_006508.2
KEGG	hsa:6567
String	9606.ENSP00000465734
Molecular Weight	Calculated MW: 60 kDa Observed MW: 70 kDa
Buffer	PBS, pH 7.3, containing 0.01% thimerosal, 50% glycerol.
Concentration	> 0.2 mg/ml
Availability	Shipped within 5-10 working days.
Note	This product is for research use only.

Research Articles on Solute Carrier Family 16 Member 2 (SLC16A2)

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