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Browse our Iodotyrosine Deiodinase (IYD) ELISA Kits

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Iodotyrosine Deiodinase ELISA Kits (IYD)
On are 4 Iodotyrosine Deiodinase (IYD) ELISA Kits from 1 different suppliers available. Additionally we are shipping Iodotyrosine Deiodinase Antibodies (15) and Iodotyrosine Deiodinase Proteins (8) and many more products for this protein. A total of 30 Iodotyrosine Deiodinase products are currently listed.
0610009A07Rik, AI265638, C6orf71, Dehal1, dJ422F24.1, IYD-1, MGC85450, RGD1309288, TDH4

Iodotyrosine Deiodinase (IYD) ELISA Kits by Reactivity

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Xenopus laevis Iodotyrosine Deiodinase (IYD) interaction partners

  1. findings suggest that IYD transcription is activated by TH receptors early during intestinal remodeling to ensure efficient iodine recycling at the climax of metamorphosis when high levels of TH are needed for proper transformations of different organs.

Human Iodotyrosine Deiodinase (IYD) interaction partners

  1. The rate-limiting processes that contribute to the ability of flavin to promote reductive dehalogenation in human IYD.

  2. A switch between one- and two-electron chemistry of iodotyrosine deiodinase is controlled by substrate.

  3. Iodotyrosine deiodinase defect identified via genome-wide approach.

  4. high activity of human saliva (show RAG1AP1 ELISA Kits) peroxidase with iodide as a substrate may play a crucial role in the bioavailability and metabolism of biologically active iodide.

  5. Mutations in DEHAL1 leads to hypothyroidism, goiter and mental retardation (Review)

  6. molecular cloning and investigation of the localization and activity of DEHAL1

  7. the cytoplasmic tail of DEHAL1 could play a role in the stability of the protein

  8. Diffuse cytoplasmatic localisation or downregulation of DEHAL1 expression in thyroid cancers suggests alteration or loss of DEHAL1 function during thyroid cell dedifferentiation.

  9. homozygous mutations in DEHAL1 appear to cause human iodotyrosine deiodinase deficiency, leading to hereditary hypothyroidism and goiter

  10. This study describes a functional mutation within IYD, demonstrating the molecular basis of the iodine wasting form of congenital hypothyroidism

Mouse (Murine) Iodotyrosine Deiodinase (IYD) interaction partners

  1. At least for Metazoa, IYD should provide a new marker for tracing the evolutionary development of iodinated amino acids as regulatory signals through the tree of life.

  2. Data show that the structures provide a molecular basis for understanding thyroid disease based on mutations of IYD.

Iodotyrosine Deiodinase (IYD) Antigen Profile

Antigen Summary

This gene encodes an enzyme that catalyzes the oxidative NADPH-dependent deiodination of mono- and diiodotyrosine, which are the halogenated byproducts of thyroid hormone production. The N-terminus of the protein functions as a membrane anchor. Mutations in this gene cause congenital hypothyroidism due to dyshormonogenesis type 4, which is also referred to as deiodinase deficiency, or iodotyrosine dehalogenase deficiency, or thyroid hormonogenesis type 4. Alternative splicing results in multiple transcript variants.

Alternative names and synonyms associated with Iodotyrosine Deiodinase (IYD)

  • iodotyrosine deiodinase (IYD) Elisa Kit
  • iodotyrosine deiodinase (iyd) Elisa Kit
  • iodotyrosine deiodinase (Iyd) Elisa Kit
  • 0610009A07Rik Elisa Kit
  • AI265638 Elisa Kit
  • C6orf71 Elisa Kit
  • Dehal1 Elisa Kit
  • dJ422F24.1 Elisa Kit
  • IYD-1 Elisa Kit
  • MGC85450 Elisa Kit
  • RGD1309288 Elisa Kit
  • TDH4 Elisa Kit

Protein level used designations for IYD

iodotyrosine deiodinase , iodotyrosine dehalogenase 1 , IYD-1 , iodotyrosine dehalogenase 1 protein

421631 Gallus gallus
447152 Xenopus laevis
472159 Pan troglodytes
476244 Canis lupus familiaris
496718 Xenopus (Silurana) tropicalis
534110 Bos taurus
705471 Macaca mulatta
389434 Homo sapiens
70337 Mus musculus
308129 Rattus norvegicus
403124 Sus scrofa
100127058 Pongo abelii
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