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Transmembrane Protease, Serine 3 (TMPRSS3) (N-Term) Peptid

TMPRSS3 Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN8114416
168,15 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 6 bis 9 Werktagen

Kurzübersicht für Transmembrane Protease, Serine 3 (TMPRSS3) (N-Term) Peptid (ABIN8114416)

Target

TMPRSS3 (Transmembrane Protease, Serine 3 (TMPRSS3))

Spezies

Human

Quelle

  • 10
Synthetic

Applikation

Blocking Peptide (BP), Western Blotting (WB)
  • Protein Region

    N-Term

    Verwendungszweck

    TMPRSS3 Peptide - N-terminal region

    Sequenz

    MGENDPPAVE APFSFRSLFG LDDLKISPVA PDADAVAAQI LSLLPLKFFP
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Kommentare

    This is a synthetic peptide designed for use in combination with anti-TMPRSS3 Antibody(ARP57683_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

    TMPRSS3 (Transmembrane Protease, Serine 3 (TMPRSS3))

    Hintergrund

    Background Information: This gene encodes a protein that belongs to the serine protease family. The encoded protein contains a serine protease domain, a transmembrane domain, a LDL receptor-like domain, and a scavenger receptor cysteine-rich domain. Serine proteases are known to be involved in a variety of biological processes, whose malfunction often leads to human diseases and disorders. This gene was identified by its association with both congenital and childhood onset autosomal recessive deafness. This gene is expressed in fetal cochlea and many other tissues, and is thought to be involved in the development and maintenance of the inner ear or the contents of the perilymph and endolymph. This gene was also identified as a tumor associated gene that is overexpressed in ovarian tumors. Alternatively spliced transcript variants have been described.

    Alternative Symbols: DFNB10, DFNB8, ECHOS1, TADG12

    Molekulargewicht

    50kDa

    Gen-ID

    64699

    NCBI Accession

    NP_076927

    UniProt

    P57727
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