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Claudin 5 (CLDN5) (C-Term) Peptide

CLDN5 Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN975043

Aperçu rapide pour Claudin 5 (CLDN5) (C-Term) Peptide (ABIN975043)

Antigène

Claudin 5 (CLDN5)

Origine

Humain

Source

  • 2
Synthetic

Application

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

    C-Term

    Attributs du produit

    This is a synthetic peptide designed for use in combination with anti-CLDN5 antibody (Catalog #: ARP33627_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.

    Purification

    Purified
  • Indications d'application

    Each Investigator should determine their own optimal working dilution for specific applications.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

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

    Concentration

    1 mg/mL

    Buffer

    Final peptide concentration is 1 mg/mL in PBS.

    Conseil sur la manipulation

    Avoid repeated freeze-thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

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

    Claudin 5 (CLDN5)

    Sujet

    CLDN5 is a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets. Mutations in this gene have been found in patients with velocardiofacial syndrome.This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets. Mutations in this gene have been found in patients with velocardiofacial syndrome. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

    Alias Symbols: AWAL, BEC1, CPETRL1, TMVCF

    Protein Interaction Partner: CLDN3,CLDN5,MPDZ,TJP1,CLDN1,CLDN3,TJP1

    Protein Size: 218

    Poids moléculaire

    23 kDa

    ID gène

    7122

    NCBI Accession

    NM_003277, NP_003268

    UniProt

    O00501
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