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ECM1 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

ECM1 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2731598
  • Antigène Voir toutes ECM1 Protéines
    ECM1 (Extracellular Matrix Protein 1 (ECM1))
    Type de proteíne
    Recombinant
    Attributs du protein
    Transcript Variant 1
    Origine
    • 5
    • 4
    • 1
    • 1
    Humain
    Source
    • 5
    • 2
    • 2
    • 1
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette ECM1 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human Secretory component / ECM1 (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Pureté
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product ECM1 Protéine
  • Indications d'application
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Commentaires

    The tag is located at the C-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Stock
    -80 °C
    Stockage commentaire
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Antigène
    ECM1 (Extracellular Matrix Protein 1 (ECM1))
    Autre désignation
    Secretory Component,ecm1 (ECM1 Produits)
    Synonymes
    URBWD Protein, ECM Protein, EMILIN4 Protein, GPIa* Protein, MMRN Protein, AI663821 Protein, p85 Protein, extracellular matrix protein 1 Protein, multimerin 1 Protein, ECM1 Protein, MMRN1 Protein, Ecm1 Protein
    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.
    Poids moléculaire
    58.8 kDa
    NCBI Accession
    NP_004416
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