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Transthyretin (TTR) (N-Term) Peptide

TTR Reactivité: Humain Hôte: Synthetic BP
N° du produit ABIN8114579
168,15 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour Transthyretin (TTR) (N-Term) Peptide (ABIN8114579)

Antigène

TTR (Transthyretin (TTR))

Origine

Humain

Source

  • 4
  • 1
Synthetic

Application

Blocking Peptide (BP)
  • Protein Region

    N-Term

    Fonction

    TTR Peptide - N-terminal region

    Séquence

    CPLMVKVLDA VRGSPAINVA VHVFRKAADD TWEPFASGKT SESGELHGLT
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Commentaires

    This is a synthetic peptide designed for use in combination with anti-TTHY Antibody (ARP75166_P050),. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications. Please inquire for more details.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 µL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Buffer

    Lyophilized powder

    Stock

    -20 °C

    Stockage commentaire

    For longer periods of storage, store at -20 °C. Avoid repeat freeze-thaw cycles.
  • Antigène

    TTR (Transthyretin (TTR))

    Sujet

    Background Information: This gene encodes one of the three prealbumins, which include alpha-1-antitrypsin, transthyretin and orosomucoid. The encoded protein, transthyretin, is a homo-tetrameric carrier protein, which transports thyroid hormones in the plasma and cerebrospinal fluid. It is also involved in the transport of retinol (vitamin A) in the plasma by associating with retinol-binding protein. The protein may also be involved in other intracellular processes including proteolysis, nerve regeneration, autophagy and glucose homeostasis. Mutations in this gene are associated with amyloid deposition, predominantly affecting peripheral nerves or the heart, while a small percentage of the gene mutations are non-amyloidogenic. The mutations are implicated in the etiology of several diseases, including amyloidotic polyneuropathy, euthyroid hyperthyroxinaemia, amyloidotic vitreous opacities, cardiomyopathy, oculoleptomeningeal amyloidosis, meningocerebrovascular amyloidosis and carpal tunnel syndrome.

    Alternative Symbols: CTS, ATTR, CTS1, PALB, TBPA, HEL111, HsT2651

    Poids moléculaire

    16kDa

    ID gène

    7276

    NCBI Accession

    NP_000362

    UniProt

    P02766
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