Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

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

Recombinant ECM1 protein expressed in HEK-293 Cells.
Catalog No. ABIN2731598

Quick Overview for ECM1 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag) (ABIN2731598)

Target

See all ECM1 Proteins
ECM1 (Extracellular Matrix Protein 1 (ECM1))

Protein Type

Recombinant

Origin

  • 5
  • 4
  • 1
  • 1
Human

Source

  • 7
  • 2
  • 1
  • 1
HEK-293 Cells

Application

Antibody Production (AbP), Standard (STD)

Purity

> 80 % as determined by SDS-PAGE and Coomassie blue staining
  • Protein Characteristics

    Transcript Variant 1

    Purification tag / Conjugate

    This ECM1 protein is labelled with Myc-DYKDDDDK Tag.

    Characteristics

    • Recombinant human Secretory component / ECM1 (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
  • Want other Options for this Protein ?

    !
    Discover Our Predefined Custom Proteins and Custom Protein Services!

    Your project requires further customization? Contact us and discover our custom protein solutions

  • 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

    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
You are here:
Chat with us!