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anti-Monocarboxylate Transporter 8 (MCT8) Antibodies

MCT8 encodes an integral membrane protein that functions as a transporter of thyroid hormone. Additionally we are shipping Monocarboxylate Transporter 8 Proteins (4) and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
MCT8 20502 O70324
MCT8 6567 P36021
MCT8 259248 Q8K1P8
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Top anti-Monocarboxylate Transporter 8 Antibodies at antibodies-online.com

Showing 10 out of 29 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Human Rabbit Un-conjugated ELISA, WB   100 μg Log in to see 2 to 3 Days
$302.50
Details
Human Rabbit Un-conjugated WB Western blot analysis of MCT8 expression in HeLa (A), Raw264.7 (B), rat kidney (C) whole cell lysates. 200 μL Log in to see 9 Days
$487.50
Details
Human Rabbit Un-conjugated ELISA   50 μL Log in to see 8 to 10 Days
$566.50
Details
Human Rabbit Un-conjugated ELISA, WB   100 μL Log in to see 14 Days
$201.19
Details
Human Rabbit Un-conjugated WB   100 μL Log in to see 8 to 10 Days
$522.50
Details
Human Rabbit Un-conjugated WB   100 μL Log in to see 8 to 10 Days
$375.83
Details
Human Rabbit Un-conjugated IHC (p), ELISA, WB   50 μL Log in to see 8 to 10 Days
$451.00
Details
Human Rabbit Un-conjugated WB   50 μL Log in to see 8 to 10 Days
$463.83
Details
Human Rabbit Un-conjugated ELISA, WB   50 μL Log in to see 9 to 11 Days
$313.50
Details
Human Rabbit Un-conjugated ELISA, WB   100 μg Log in to see 11 to 16 Days
$412.86
Details

MCT8 Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality
Mouse (Murine) ,


Human ,


Rat (Rattus)


Top referenced anti-Monocarboxylate Transporter 8 Antibodies

  1. Human Polyclonal MCT8 Primary Antibody for ELISA, WB - ABIN1451355 : Ross, Grafham, Coffey, Scherer, McLay, Muzny, Platzer, Howell, Burrows, Bird, Frankish, Lovell, Howe, Ashurst, Fulton, Sudbrak, Wen, Jones, Hurles, Andrews, Scott, Searle, Ramser, Whittaker, Deadman et al.: The DNA sequence of the human X chromosome. ... in Nature 2005 (PubMed)

More Antibodies against Monocarboxylate Transporter 8 Interaction Partners

Cow (Bovine) Monocarboxylate Transporter 8 (MCT8) interaction partners

  1. immunohistochemical studies localized MCT2 (show SLC16A7 Antibodies), MCT7, and MCT8 proteins in the cattle rumen, abomasum, jejunum, and caecum.

Mouse (Murine) Monocarboxylate Transporter 8 (MCT8) interaction partners

  1. Data indicate silymarin, an extract of the milk thistle, to be a potent inhibitor of T3 thyroid hormone (show PTH Antibodies) uptake by solute carrier (show SERTAD2 Antibodies) family 16 (monocarboxylic acid transporters), member 2 protein (MCT8).

  2. Data show that diiodothyropropionic acid (DITPA) mainly ameliorated the hypermetabolism of monocarboxylate transporter 8 (MCT8) knockout mice.

  3. The data demonstrate that OATP1c1 (show SLCO1C1 Antibodies) and MCT8 expression are regulated in a parallel manner during inflammation at the blood-brain barrier of rodents.

  4. This study showed that mouse MCT1 (show MCTS1 Antibodies), MCT2 (show SLC16A7 Antibodies), and MCT4 (show SLC16A3 Antibodies) are expressed in the PNS. While DRG neurons express MCT1 (show MCTS1 Antibodies), myelinating Schwann cells.

  5. Cerebral cortex hyperthyroidism of newborn mct8-deficient mice transiently suppressed by lat2 (show SLC7A8 Antibodies) inactivation.

  6. Mct8 deficiency has important metabolic consequences in the brain

  7. Transporters MCT8 and OATP1C1 (show SLCO1C1 Antibodies) maintain murine brain thyroid hormone (show PTH Antibodies) homeostasis.

  8. in Parkinson's disease, the levels of MCT1 (show MCTS1 Antibodies), MCT2 (show SLC16A7 Antibodies) and GLUT1 (show SLC2A1 Antibodies) is not changed following dopaminergic neurodegeneration

  9. Mct10 (show SLC16A10 Antibodies) participates in tissue-specific TH transport and also contributes to the generation of the unusual serum TH profile characteristic for Mct8 deficiency

  10. These studies indicate that the high serum T3 in MCT8 deficiency increases the total energy expenditure and fails to maintain weight despite adequate calorie intake.

Human Monocarboxylate Transporter 8 (MCT8) interaction partners

  1. MCT8 Mutation is associated with Allan-Herndon-Dudley Syndrome.

  2. brain damage in MCT8 deficiency is diffuse, without evidence of focal lesions, and present from fetal stages despite apparent normality at birth

  3. Specific mutations of MCT8 located in transmembrane helix 2 (del230F, V235M, and ins236V) increase the capacity of MCT8 variants to dimerize.

  4. we report 4 Allan-Herndon-Dudley syndrome patients in unrelated Turkish families harboring novel MCT8 mutations

  5. two SNPs in MCT8 were related to circulating thyroid hormone (show PTH Antibodies) levels in men but not in women: the rs5937843 polymorphism (G/T) was inversely associated with FT4 levels and the rs6647476 (T/C) polymorphism related negatively to circulating FT3

  6. A reduction in MCT8 expression in the intrauterine growth retardation fetal brain could further compromise Thyroid hormone (show PTH Antibodies)-dependent brain development.

  7. We describe three new SLC16A2 mutations associated with different levels of clinical severity in patients with psychomotor retardation disorders.

  8. Monocarboxylate transporter 8 modulates the viability and invasive capacity of human placental cells and fetoplacental growth in mice.

  9. A boy with Allan-Herndon-Dudley syndrome and his heterozygous mother had a point mutation in exon 3 of the MCT8 gene 1201G>A:G401R which changes the properties of the protein.

  10. MCT8 mutations in Allan-Herndon-Dudley Syndrome patients may have tissue-specific effects on thyroid hormone (show PTH Antibodies) transport.

Monocarboxylate Transporter 8 (MCT8) Antigen Profile

Protein Summary

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.

Gene names and symbols associated with MCT8

  • solute carrier family 16, member 2 (monocarboxylic acid transporter 8) (SLC16A2) antibody
  • solute carrier family 16 (monocarboxylic acid transporters), member 2 (Slc16a2) antibody
  • solute carrier family 16, member 2 (thyroid hormone transporter) (SLC16A2) antibody
  • solute carrier family 16, member 2 (thyroid hormone transporter) (Slc16a2) antibody
  • AHDS antibody
  • AW105741 antibody
  • DXS128 antibody
  • DXS128E antibody
  • MCT7 antibody
  • MCT 7 antibody
  • Mct8 antibody
  • MCT 8 antibody
  • MRX22 antibody
  • XPCT antibody

Protein level used designations for MCT8

monocarboxylate transporter 8 , MCT 8 , Monocarboxylate transporter 8 (MCT 8) (X-linked PEST-containing transporter) , X-linked PEST-containing transporter , solute carrier family 16 member 2 , monocarboxylate transporter 7 , solute carrier family 16 (monocarboxylic acid transporters), member 2 , solute carrier family 16, member 2 (monocarboxylic acid transporter 8)

GENE ID SPECIES
535872 Bos taurus
20502 Mus musculus
6567 Homo sapiens
259248 Rattus norvegicus
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