Human PD-L2 (CD273) Antibody (clone 24F.10C12)

Mouse IgG2a - Recombinant

ABOUT

Recombinant anti-human PD-L2 - For Bio IC™ assay and detection

Anti-hPD-L2-mIgG2a is a recombinant monoclonal antibody (mAb) designed for use with PD-1/PD-L2 cellular assays to study immune checkpoint (IC) modulation. This mAb is derived from the 24F.10C12 clone, targeting the human programmed death ligand 2 (hPD-L2, aka CD273).

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Anti-hPD-L2-mIgG2a can be used as a benchmark antibody in our PD-1/PD-L2 Bio IC™ cellular assay, which is designed to screen antagonists, such as antibodies, Fc-fusion proteins, or small molecules, targeting the PD-1/PD-L2 axis. In addition, it is suitable for use in flow cytometry (see figures).

 

Key features

  • Each lot is functionally tested and validated
  • The complete sequence of the antibody construct has been verified
  • Absence of endotoxins determined by the EndotoxDetect™ assay

All products are for research use only, and not for human or veterinary use.

SPECIFICATIONS

Specifications

Target

PD-L2, CD273

Target species

Human

Species
Human
Isotype
mIgG2a
kappa
Clone
24F.10C12
Molecular weight
145 kDa
Tag
Tag-free
Source
CHO cells
Purification
Protein A
Formulation buffer

Sodium phosphate buffer with glycine, saccharose, and stabilizing agents

Preservative
Azide-free
Purity
≥ 95%
Appearance (form)
Lyophilized
Reconstitution buffer
Sterile water (not provided)
Endotoxin

Negative (tested using EndotoxDetect™ assay)

Tested applications

PD-1/PD-L2 Bio IC™ assay, flow cytometry

Quality control

Each lot is functionally tested by flow cytometry.

CONTENTS

Contents

  • Product: 
    Anti-hPD-L2-mIgG2a
  • Cat code: 
    hpdl2-mab10
  • Quantity: 
    100 µg

Shipping & Storage

  • Shipping method:  Room temperature
  • Storage:

    • -20 °C
    Stability: -20 °C for up to 1 year

    Caution:

    • Avoid repeated freeze-thaw cycles

Details

Programmed cell death ligand 2 (PD-L2), also known as cluster of differentiation 273 (CD273) or B7-DC, is a transmembrane protein that is mostly expressed by antigen-presenting cells, such as dendritic cells and macrophages [1]. It serves as a second ligand for programmed cell death protein 1 (PD-1), complementing PD-L1 in mediating peripheral immune tolerance and maintaining immune homeostasis during infection [1, 2].

When PD-L2 binds to PD-1 on T cells, it inhibits T cell receptor (TCR) signaling, reduces cytokine production, and limits T cell proliferation—mechanisms essential for preventing excessive immune activation. Like PD-L1, PD-L2 is also co-opted by cancer cells and tumor-associated immune cells to suppress T cell-dependent anti-tumor immunity [2,3]. 

Elevated PD-L2 expression has been observed in various malignancies, including lung, colorectal, as well as breast cancers, and is often associated with poor prognosis [4]. The continuous exploration of the clinical application of PD-L2 has brought exciting prospects for promoting cancer treatment, including small molecules, PD-L2-specific vaccines, and monoclonal antibodies (mAbs) [4]. However, the clinical approval of PD-L2-specific therapeutics for tumor treatment remains elusive, necessitating further investigation and discovery [4].

 

References

1. Latchman, Y. et al. 2001. PD-L2 is a second ligand for PD-1 and inhibits T cell activation. Nat Immunol 2, 261–268.
2. Yearley, J.H. et al. 2017. PD-L2 expression in human tumors: relevance to anti-PD-1 therapy in cancer. Clin Cancer Res 23, 3158–3167.
3. Rozali, E.N. et al. 2012. Programmed death ligand 2 in cancer-induced immune suppression. Clin Dev Immunol 2012, 656340.
4. Yang Y, et al. 2024. Programmed cell death-ligand 2: new insights in cancer. Front Immunol. 2024 Mar 28;15:1359532.

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