Recombinant Mouse Active Heparanase/HPSE Protein, CF

R&D Systems | Catalog # 9788-GH

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Key Product Details

  • R&D Systems NS0-derived Recombinant Mouse Active Heparanase/HPSE Protein (9788-GH)
  • Quality control testing to verify active proteins with lot specific assays by in-house scientists
  • All R&D Systems proteins are covered with a 100% guarantee

Source

NS0

Accession Number

Q6YGZ1

Applications

Enzyme Activity
View all Heparanase/HPSE Proteins and Enzymes »

Product Specifications

Source

Mouse myeloma cell line, NS0-derived mouse Heparanase/HPSE protein
Asp28-Ile535, with an N-terminal 6-His tag

Purity

>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.

Endotoxin Level

<1.0 EU per 1 μg of the protein by the LAL method.

N-terminal Sequence Analysis

Glu146 and Lys150

Predicted Molecular Mass

43 kDa (50 kDa subunit) and 9 kDa (8 kDa subunit)

SDS-PAGE

40-58 kDa (50 kDa subunit) and 8-12 kDa (8 kDa subunit), reducing conditions

Activity

Measured by its ability to release biotinylated heparan sulfate from Recombinant Human Syndecan‑4 (Catalog # 2918-SD).
20 ng rmHPSE digestion will result in >50% of OD reduction compared with the Negative Control.

Formulation, Preparation, and Storage

9788-GH
Formulation Supplied as a 0.2 μm filtered solution in Tris, NaCl and E64.
Reconstitution
Shipping The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.
Stability & Storage Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
  • 6 months from date of receipt, -20 to -70 °C as supplied.
  • 3 months, -20 to -70 °C under sterile conditions after opening.

Background: Heparanase/HPSE

Heparanase (HPSE) selectively cleaves heparan sulfate (HS) at specific sites on HS proteoglycans (HSPGs) (1, 2, 3, 4). The enzyme is synthesized as an inactive 65 kDa proenzyme that is secreted via the Golgi apparatus and associates with the cell membrane through interaction with HSPGs (5). It is then endocytosed and transferred to lysosomes (6) where cathepsin L activates it by removing an internal inhibitory peptide, forming a heterodimer composed of an 8 kDa and a 50 kDa subunit (7, 8). Under certain stimuli, the active enzyme is transferred back to the cell surface, where it participates in extracellular matrix degradation and remodeling (9). HPSE facilitates cell migration associated with metastasis, wound healing and inflammation (10). An increase in its activity is associated with an increase in VEGF activity, which further enhances angiogenesis (11). HPSE also enhances shedding of syndecans and increases endothelial invasion and angiogenesis in myelomas (12). It acts as a procoagulant by increasing the generation of activation factor X in the presence of tissue factor and activation factor VII (13). In addition, it increases cell adhesion to the extracellular matrix (ECM), independent of its enzymatic activity (14). HPSE is highly expressed in placenta and spleen and weakly expressed in lymph node, thymus, peripheral blood leukocytes, bone marrow, endothelial cells, fetal liver and tumor tissues (15). Mouse HPSE shows 76% identity to human HPSE at amino acid sequence. The enzyme activity of recombinant mouse HPSE was assayed using recombinant syndecan 4 that was biotinylated at the non-reducing end of its HS chains (catalogue ES020) in ELISA format (16).

Alternate Names

Endo-glucoronidase, HPA1, HPR1, HPSE, HSE1

Entrez Gene IDs

10855 (Human); 15442 (Mouse); 64537 (Rat)

Gene Symbol

HPSE

UniProt

Q6YGZ1

Additional Heparanase/HPSE Products

Product Documents for Recombinant Mouse Active Heparanase/HPSE Protein, CF

Certificate of Analysis

To download a Certificate of Analysis, please enter a lot or batch number in the search box below.

Note: Certificate of Analysis not available for kit components.

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Manufacturing Specifications

  1. Vlodavsky, I. et al. (1999) Nat. Med. 5:793.
  2. Hulett, M.D. et al. (1999) Nat. Med. 5:803.
  3. Gong, F. et al. (2003) J. Biol. Chem. 278:35152.
  4. Peterson, S.B. and Liu, J. (2010) J. Biol. Chem. 285:14504.
  5. Nadav L. et al. (2002) J. Cell Sci. 115:2179.
  6. Gingis-Velitski, S. et al. (2004) J. Biol. Chem. 279:44084.
  7. Abboud-Jarrous, G. et al. (2008) J. Biol. Chem. 283:18167.
  8. Zetser, A. et al. (2004) J. Cell Sci. 117:2249.
  9. Zcharia E. et al. (2001) J. Mammary Gland Biol. Neoplasia 6:311.
  10. Fux, L. et al. (2009) Trends Biochem. Sci. 34:511.
  11. Cohen-Kaplan, V. et al. (2008) Int. J. Cancer 123:2566.
  12. Purushothaman, A. et al. (2010) Blood 115:2449.
  13. Nadir, Y. et al. (2010) Haematologica 95:1927.
  14. Goldshmidt, O. et al. (2003) FASEB J. 17:1015.
  15. Kussie, P.H. et al. (1999) Biochem. Biophys. Res. Commun. 261:183.
  16. Wu, Z.L. et al. (2017) Glycobiology 27:518.

Product Specific Notices for Recombinant Mouse Active Heparanase/HPSE Protein, CF

For research use only

Citations for Recombinant Mouse Active Heparanase/HPSE Protein, CF

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Protocols

View specific protocols for Recombinant Mouse Active Heparanase/HPSE Protein, CF (9788-GH):

Materials
  • Assay Buffer: 50 mM Sodium Acetate, pH 5.0
  • Recombinant Mouse Heparanase/HPSE (rmHPSE) (Catalog # 9788-GH)
  • HPSE Substrate/ (Catalog # ES020)
  • Human Syndecan-4 DuoSet Kit (Catalog # DY2918)
  • 96-well Clear Plate (Catalog # DY990)
  • Plate Reader (Model: SpectraMax Plus by Molecular Devices) or equivalent

    And the following materials that are routinely used in ELISA

  • Coating Buffer (Catalog # DY006)
  • Wash Buffer (25X) (Catalog # WA126)
  • Reagent Diluent (10X) (Catalog # DY995)
  • Substrate Reagent Pack (Catalog # DY999)
  • Stop Solution (Catalog # DY994)
  1. Prepare an ELISA plate by following the DuoSet kit protocol.
  2. Dilution factor determination:
    a. Dilute the HPSE Substrate stock 100-fold in Reagent Diluent (this will be the first dilution point).
    b. Further prepare a 2-fold serial dilution series of the above diluted HPSE Substrate with Reagent Diluent for 6 points.
    c. Load 100 µL of each point onto the prepared ELISA plate in duplicate. Load 100 µL of Reagent Diluent to 2 separate wells for blank control.
    d. Cover the plate and incubate at room temperature for 2 hours.
    e. Follow the DuoSet Assay Procedure from step 4 to step 9 to complete the assay.
    f. Determine the dilution factor (n) that achieves an OD between 1.8-3.0.
  3. rmHPSE Activity Detection:
    a. Dilute the HPSE Substrate stock by n/10-fold in Assay Buffer.
    b. Combine 10 µL of rmHPSE with 10 µL of the diluted HPSE Substrate in a vial. For negative control, combine 10 µL of  Assay Buffer and 10 µL of the diluted HPSE Substrate in a vial.
    c. Incubate reactions and negative control at 37 °C for 2 hours.
    d. After incubation, heat all reactions and negative control at 95 °C for 2 minutes to inactivate rmHPSE.
    e. Add 220 µL of Reagent Diluent to each reaction and negative control. Mix well.
    f. Load 100 µL of each sample onto the prepared ELISA plate in duplicate.
    g. Cover the plate and incubate for 2 hours at room temperature.
    h. Follow the DuoSet Assay Procedure from step 4 to step 9 to complete the assay.
  4. Calculate % OD reduction compared with the negative control:

    [1-(OD of the wells of rmHPSE treated/OD of the wells of negative control)] x 100 = % OD reduction

Per Reaction:

  • rmHPSE: 20 ng

FAQs

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Associated Pathways

Articular Cartilage Extracellular Matrix Articular Cartilage Extracellular Matrix Thumbnail