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Sovipostobart

(Synonyms: BMS-986249)
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Based on 1 Customer Validation

Sovipostobart is an immunoglobulin G1-kappa, anti-CTLA-4 human monoclonal antibody with cleavable prodomain. Sovipostobart is an immunostimulant and antineoplastic.

Nur für Forschungszwecke. Wir verkaufen nicht an Patienten.

  • Reinheit : 96.528%
  • CAS. Nr.: 2649371-19-5
  • Molecular Weight:153.531 kDa
  • Speicherung:
    Shipping with dry ice

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

  • Experimental Validation Results for Sovipostobart
  • Experimental Validation Results for Sovipostobart
  • Experimental Validation Results for Sovipostobart
  • Sovipostobart Chemical Structure
    Sovipostobart Chemical Structure
CAS. Nr.: 2649371-19-5
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Tel: 609-228-6898 E-mail: [email protected] [email protected]

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Sovipostobart Product Recommendations:

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

609-228-6898
[email protected] [email protected]
Finden Sie Ihren Händler vor Ort Your local distributor: Hycultec GmbHHycultec
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Assay Types
  • 1/16

    Human IgG1 kappa

  • 1/16

    Immobilized CTLA-4 Protein, Human (HEK293, HY-P72959) can bind Sovipostobart. The EC50 for this effect is 17.01 ng/mL.

  • 1/16

    Flow Cytometry analysis of Raji cells labelling CTLA4 (red) with Sovipostobart (anti-CTLA4) (HY-P990080). 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 IgG1 kappa (HY-P99001, blue) was used as the isotype control, cells without incubation with primary antibody were used as the unlabeled control (black).

  • Sovipostobart Chemical Structure
    1/16
  • Sovipostobart
  • Immobilized CTLA-4 Protein, Human (HEK293, HY-P72959) can bind Sovipostobart. The EC50 for this effect is 17.01 ng/mL.
  • Flow Cytometry analysis of Raji cells labelling CTLA4 (red) with Sovipostobart (anti-CTLA4) (HY-P990080). 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 IgG1 kappa (HY-P99001, blue) was used as the isotype control, cells without incubation with primary antibody were used as the unlabeled control (black).