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Transthyretin (TTR) (N-Term) Peptid

TTR Reaktivität: Human Wirt: Synthetic BP
Produktnummer ABIN8114579
168,15 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 6 bis 9 Werktagen

Kurzübersicht für Transthyretin (TTR) (N-Term) Peptid (ABIN8114579)

Target

TTR (Transthyretin (TTR))

Spezies

Human

Quelle

  • 4
  • 1
Synthetic

Applikation

Blocking Peptide (BP)
  • Protein Region

    N-Term

    Verwendungszweck

    TTR Peptide - N-terminal region

    Sequenz

    CPLMVKVLDA VRGSPAINVA VHVFRKAADD TWEPFASGKT SESGELHGLT
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Kommentare

    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.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

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

    Buffer

    Lyophilized powder

    Lagerung

    -20 °C

    Informationen zur Lagerung

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

    TTR (Transthyretin (TTR))

    Hintergrund

    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

    Molekulargewicht

    16kDa

    Gen-ID

    7276

    NCBI Accession

    NP_000362

    UniProt

    P02766
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