Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

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

TMPRSS3 Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN8114416
168,15 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour Transmembrane Protease, Serine 3 (TMPRSS3) (N-Term) Peptide (ABIN8114416)

Antigène

TMPRSS3 (Transmembrane Protease, Serine 3 (TMPRSS3))

Origine

Humain

Source

  • 10
Synthetic

Application

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

    N-Term

    Fonction

    TMPRSS3 Peptide - N-terminal region

    Séquence

    MGENDPPAVE APFSFRSLFG LDDLKISPVA PDADAVAAQI LSLLPLKFFP
  • 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-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.

    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

    TMPRSS3 (Transmembrane Protease, Serine 3 (TMPRSS3))

    Sujet

    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

    Poids moléculaire

    50kDa

    ID gène

    64699

    NCBI Accession

    NP_076927

    UniProt

    P57727
Vous êtes ici:
Chat with us!