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

ECM1 Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN2182498
  • Target Alle ECM1 Produkte
    ECM1 (Extracellular Matrix Protein 1 (ECM1))
    Protein Region
    Middle Region
    Spezies
    Human
    Quelle
    • 1
    Synthetic
    Applikation
    Blocking Peptide (BP), Western Blotting (WB)
    Sequenz
    QDRSQGGWGH RLDGFPPGRP SPDNLNQICL PNRQHVVYGP WNLPQSSYSH
    Produktmerkmale
    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.
    Aufreinigung
    Purified
  • Applikationshinweise
    Optimal working dilution should be determined by the investigator.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Konzentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Handhabung
    Avoid repeat freeze-thaw cycles.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    ECM1 (Extracellular Matrix Protein 1 (ECM1))
    Synonyme
    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
    Hintergrund
    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
    Molekulargewicht
    18 kDa
    Gen-ID
    1893
    NCBI Accession
    NM_022664, NP_073155
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