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Ongericimab

(Synonyms: JS002)
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Based on 1 Customer Validation

Ongericimab (JS002) is a humanized anti-PCSK9 monoclonal antibody. Ongericimab has lipid-lowering efficacy. Ongericimab can be used in research of hypercholesteremia and hyperlipidemia.

For research use only. We do not sell to patients.

  • Storage:
    Shipping with dry ice

    Please store the product under the recommended conditions in the Certificate of Analysis.

  • Experimental Validation Results for Ongericimab
  • Experimental Validation Results for Ongericimab
  • Experimental Validation Results for Ongericimab
  • Ongericimab Chemical Structure
    Ongericimab Chemical Structure
CAS No.: 2145096-91-7
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Tel: 609-228-6898 E-mail: [email protected] [email protected]

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Ongericimab Product Recommendations:

To place orders, for customer services and technical support, please contact:

609-228-6898
[email protected] [email protected]
Find Your Local Distributor Your local distributor: Hycultec GmbHHycultec
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Assay Types
  • 1/16

    Human IgG4 kappa

  • 1/16

    Immobilized PCSK9 Protein, Human (HEK293, C-His, HY-P70545A) can bind Ongericimab. The EC50 for this effect is 5.198 ng/mL.

  • 1/16

    Flow Cytometry analysis of Hela cells labelling PCSK9 (red) with Ongericimab (anti-PCSK9) (HY-P99773). Cells were fixed with 4% paraformaldehyde and permeabilised with 90% methanol. Then cells were stained with the primary antibody at 1/200 dilution for an hour at 4℃. Goat Anti-Human IgG H&L (AF488) (HY-P83776) was used as the secondary antibody at 1/1,000 dilution for 30 minutes at 4℃. Human IgG4 kappa (HY-P99003, blue) was used as the isotype control, cells without incubation with primary antibody were used as the unlabeled control (black).

  • Ongericimab Chemical Structure
    1/16
  • Ongericimab
  • Immobilized PCSK9 Protein, Human (HEK293, C-His, HY-P70545A) can bind Ongericimab. The EC50 for this effect is 5.198 ng/mL.
  • Flow Cytometry analysis of Hela cells labelling PCSK9 (red) with Ongericimab (anti-PCSK9) (HY-P99773). Cells were fixed with 4% paraformaldehyde and permeabilised with 90% methanol. Then cells were stained with the primary antibody at 1/200 dilution for an hour at 4℃. Goat Anti-Human IgG H&L (AF488) (HY-P83776) was used as the secondary antibody at 1/1,000 dilution for 30 minutes at 4℃. Human IgG4 kappa (HY-P99003, blue) was used as the isotype control, cells without incubation with primary antibody were used as the unlabeled control (black).