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Anti-TREM2 Antibody (AL2p-58)

Customer Review

Based on 1 Customer Validation

Anti-TREM2 Antibody (AL2p-58) is a humanized IgG1 monoclonal antibody targeting TREM2. Anti-TREM2 Antibody (AL2p-58) can be used for the research of neuroinflammation. Recommend Isotype Controls: Human IgG1 kappa, Isotype Control (HY-P99001).

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

  • Purity : 97.43%
  • Molecular Weight:147.2 kDa
  • Storage:

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

  • Experimental Validation Results for Anti-TREM2 Antibody (AL2p-58)
  • Anti-TREM2 Antibody (AL2p-58) Chemical Structure
    Anti-TREM2 Antibody (AL2p-58) Chemical Structure
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To place orders, for customer services and technical support, please contact: MedChemExpress USA

Tel: 609-228-6898 E-mail: [email protected] [email protected]

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Anti-TREM2 Antibody (AL2p-58) 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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Top Publications Citing

Use of MCE Products

All TREM receptor Isoforms

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  • 1/16

    Flow Cytometry analysis of THP-1 cells labelling TREM2 (red) with Anti-TREM2 Antibody (HY-P991174). 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 IgG1 kappa (HY-P99001, blue) was used as the isotype control, cells without incubation with primary antibody were used as the unlabeled control (black).

  • Anti-TREM2 Antibody (AL2p-58) Chemical Structure
    1/16
  • Anti-TREM2 Antibody (AL2p-58)
  • Flow Cytometry analysis of THP-1 cells labelling TREM2 (red) with Anti-TREM2 Antibody (HY-P991174). 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 IgG1 kappa (HY-P99001, blue) was used as the isotype control, cells without incubation with primary antibody were used as the unlabeled control (black).