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Extracellular Matrix Protein 1 (ECM1) (Middle Region) Peptide

ECM1 Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN2182498
  • Antigène Tous les produits ECM1
    ECM1 (Extracellular Matrix Protein 1 (ECM1))
    Protein Region
    Middle Region
    Origine
    Humain
    Source
    • 1
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Séquence
    QDRSQGGWGH RLDGFPPGRP SPDNLNQICL PNRQHVVYGP WNLPQSSYSH
    Attributs du produit
    This is a synthetic peptide designed for use in combination with anti-ECM1 Antibody. 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
    Optimal working dilution should be determined by the investigator.
    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 repeat freeze-thaw cycles.
    Stock
    -20 °C
    Stockage commentaire
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Antigène
    ECM1 (Extracellular Matrix Protein 1 (ECM1))
    Synonymes
    URBWD Peptide, ECM Peptide, EMILIN4 Peptide, GPIa* Peptide, MMRN Peptide, AI663821 Peptide, p85 Peptide, extracellular matrix protein 1 Peptide, multimerin 1 Peptide, ECM1 Peptide, MMRN1 Peptide, Ecm1 Peptide
    Sujet
    This gene encodes a soluble protein that is involved in endochondral bone formation, angiogenesis, and tumor biology. It also interacts with a variety of extracellular and structural proteins, contributing to the maintenance of skin integrity and homeostasis. Mutations in this gene are associated with lipoid proteinosis disorder (also known as hyalinosis cutis et mucosae or Urbach-Wiethe disease) that is characterized by generalized thickening of skin, mucosae and certain viscera. Alternatively spliced transcript variants encoding distinct isoforms have been described for this gene.

    Alias Symbols: -

    Protein Size: 170
    Poids moléculaire
    18 kDa
    ID gène
    1893
    NCBI Accession
    NM_022664, NP_073155
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