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SLC16A2 Antibodies

AND SLC16A2 ELISA kits, SLC16A2 Proteins

Many biological assays use antibodies to detect SLC16A2, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with SLC16A2 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop SLC16A2 antibodies...

We validate the specificity of these antibodies to SLC16A2 by testing them on tissues known to express SLC16A2 positively and negatively. Browse below to find the SLC16A2 antibody that suites your experiment. We have 2 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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SLC16A2 Infographic by Boster Bio

SLC16A2 protein infographic

All SLC16A2 Products

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Specificity

Applications

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SLC16A2 (NM_006517) Human Over-expression Lysate

SLC16A2 Human Over-expression Lysates NM_006517

SLC16A2 Human Over-expression Lysates NM_006517

Human

$960
Cat # LS006567
20 µg, 100 µg

Anti-SLC16A2 Antibody Picoband®

Western blot analysis of SLC16A2 using anti-SLC16A2 antibody (A02662-2)

Western blot analysis of SLC16A2 using anti-SLC16A2 antibody (A02662-2)

Flow Cytometry analysis of U251 cells using anti-SLC16A2 antibody (A02662-2)

Human, Mouse, Rat

Flow Cytometry, WB

$370
Cat # A02662-2
100 μg/vial

SLC16A2 Overview

Facts about Monocarboxylate transporter 8.

SLC16A2 3D structure

SLC16A2 3D structure. Source: alphafold

Monocarboxylate transporter 8 (SLC16A2)

Very active and specific thyroid hormone transporter. Stimulates cellular uptake of thyroxine (T4), triiodothyronine (T3), reverse triiodothyronine (rT3) and diidothyronine.

Does not transportation Leu, Phe, Trp or Tyr. .

Gene Information

Human
Gene Name:	SLC16A2
Uniprot:	P36021
Entrez:	6567

Gene Information

Family

Belongs to:

major facilitator superfamily

Family

Alternative Names

AHDS; DXS128; DXS128E; MCT 7; MCT 8; MCT8; MRX22; SLC16A2; solute carrier family 16, member 2 (monocarboxylic acid transporter 8); XPCT

Molecular Weight

Mass (kDA):
59.511 kDA

Molecular Weight

Genomic Context


Human

Location:	Xq13.2
Sequence:	X; NC_000023.11 (74421493..74533916)

Tissue Specificity

Highly expressed in liver and heart.

Subcellular Localizations

Cell membrane; Multi-pass membrane protein.

Subcellular Localization

Diseases

Hypothyroidism
Allan-herndon-dudley Syndrome (ahds)
Muscle Hypotonia
Nervousness
Thyroid Hormone Resistance Syndrome
Severe Mental Retardation
Pituitary Diseases
Psychomotor Disorders
Malnutrition
Genetic Diseases, X-linked
Muscle Spasticity

Thyroid Diseases
Hypoplasia
Weakness
Dyskinetic Syndrome
Dyskinesia, Paroxysmal
Paraplegia

Disease

Pathways

Transport
Brain Development
Hormone Transport
Thyroid Hormone Transport
Secretion
Myelination
Hormone Secretion
Transmembrane Transport
Dosage Compensation
Localization
Pathogenesis
Sex Determination
Gene Silencing

Osteoblast Differentiation
Fertilization
Organic Anion Transport
Regulation Of Gene Expression
Riboflavin Transport
Translation
System Development

Pathways

PTMs

Carboxylation
Deiodination

Biotinylation
Decarboxylation

Oxidation

Bosterbio | ELISA Kits, Antibodies, Antibody Company

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/SLC16A2

References

PMID: 7981683 by Lafreniere R.G., et al. A novel transmembrane transporter encoded by the XPCT gene in Xq13.2.

PMID: 19797118 by Visser W.E., et al. Evidence for a homodimeric structure of human monocarboxylate transporter 8.