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DCBY02

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Based on 1 publication(s) in Google Scholar

DCBY02 is a monoclonal antibody targeting CD93 expressed in CHO cells. DCBY02 has a heavy chain of the mlgG type and a light chain of the mkappa type, with a predicted molecular weight (MW) of 150 kDa. The isotype control for DCBY02 can be referenced as Mouse IgG1 kappa, Isotype Control.

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  • Pureza: 98.71%
  • Peso molecular:145.78 kDa
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    Please store the product under the recommended conditions in the Certificate of Analysis.

  • Experimental Validation Results for DCBY02
  • Experimental Validation Results for DCBY02
  • DCBY02 Chemical Structure
    DCBY02 Chemical Structure
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Encuentre su distribuidor local Your local distributor: Hycultec GmbHHycultec
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  • 1/16

    Immobilized hu-CD93-ECD-his can bind DCBY02. The EC50 for this effect is 19.92 ng/mL.

  • 1/16

    Flow Cytometry analysis of THP-1 cells labelling DCBY02 (red) with DCBY02 Antibody (anti-DCBY02)(HY-P990572). 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-Mouse IgG H&L (AF488) (HY-P8005) was used as the secondary antibody at 1/1,000 dilution for 30 minutes at 4℃. Mouse IgG Isotype Control isotype Control (HY-P80757, blue) was used as the isotype control, cells without incubation with primary antibody were used as the unlabeled control (black).

  • DCBY02 Chemical Structure
    1/16
  • DCBY02
  • Immobilized hu-CD93-ECD-his can bind DCBY02. The EC50 for this effect is 19.92 ng/mL.
  • Flow Cytometry analysis of THP-1 cells labelling DCBY02 (red) with DCBY02 Antibody (anti-DCBY02)(HY-P990572). 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-Mouse IgG H&L (AF488) (HY-P8005) was used as the secondary antibody at 1/1,000 dilution for 30 minutes at 4℃. Mouse IgG Isotype Control isotype Control (HY-P80757, blue) was used as the isotype control, cells without incubation with primary antibody were used as the unlabeled control (black).