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

ECM1 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2731598
  • Target See all ECM1 Proteins
    ECM1 (Extracellular Matrix Protein 1 (ECM1))
    Protein Type
    Recombinant
    Protein Characteristics
    Transcript Variant 1
    Origin
    • 5
    • 4
    • 1
    • 1
    Human
    Source
    • 5
    • 2
    • 2
    • 1
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This ECM1 protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human Secretory component / ECM1 (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product ECM1 Protein
  • Application Notes
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Comment

    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.
    Storage
    -80 °C
    Storage Comment
    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.
  • Target
    ECM1 (Extracellular Matrix Protein 1 (ECM1))
    Alternative Name
    Secretory Component,ecm1 (ECM1 Products)
    Synonyms
    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
    Background
    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.
    Molecular Weight
    58.8 kDa
    NCBI Accession
    NP_004416
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