Anti-IL-13-Rα2-mc-MMAE ADC

CAT#: ADC-028CL

This ADC product is composed of an anti-IL-13-Rα2 antibody conjugated via mc linker to MMAE. It has demonstrated a response in IL-13-Ra2 expressing cancer treatment.

Gene Expression
Figure 1 IF staining of human cell line BJ Figure 2 IF staining of human cell line U-2 OS Figure 3 RNA cell line category: Group enriched (PC-3, U-2197, U-251 MG, U-87 MG)

Specifications

  • Antibody Overview
  • Humanized Anti-IL-13-Ra2 lgG1 Antibody
  • Linker
  • Mc (maleimidocaproyl)
  • Linker Class/Description
  • Class: Noncleavable linkers
    Description: Noncleavable linker is considered noncleavable-meaning linker cleavage, and payload release does not depend on the differential properties between the plasma and some cytoplasmic compartments. Instead, the release of the cytotoxic drug is postulated to occur after internalization of the ADC via antigen-mediated endocytosis and delivery to lysosomal compartment, where the antibody is degraded to the level of amino acids through intracellular proteolytic degradation.
  • Drug
  • N,2-dimethylalanyl-N-{(1 S,2R)-4-{(2S)-2-[(1 R,2R)-3-{[(1 S)-1-carboxy-2-phenylethyl]amino}-1-methoxy-2-methyl-3-oxopropyl]pyrrolidin-1-yl}-2-methoxy-1-[(1 S)-1-methylpropyl]-4-oxobutyl}-N-methyl-L-valinamide, trifluoroacetic acid salt

Target

  • Introduction
  • The protein encoded by this gene is closely related to Il13RA1, a subuint of the interleukin 13 receptor complex. This protein binds IL13 with high affinity, but lacks cytoplasmic domain, and does not appear to function as a signal mediator. It is reported to play a role in the internalization of IL13. [provided by RefSeq, Jul 2008]
  • Alternative Names
  • IL13RA2; interleukin 13 receptor, alpha 2; CT19; IL-13R; IL13BP; CD213A2; interleukin-13 receptor subunit alpha-2; IL-13RA2; IL-13R-alpha-2; IL-13R subunit alpha-2; cancer/testis antigen 19; IL-13 receptor subunit alpha-2; interleukin 13 binding protein; interleukin-13-binding protein; interleukin 13 receptor alpha 2 chain;
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Breast cancer biomarkers at key points during disease progression
Stable Noncleavable Linker
Comparing this noncleavable mc linker version to the cleavable version was very informative. This product showed exceptional stability. Drug release was strictly dependent on lysosomal degradation of the hu08 antibody, which we confirmed in our IL-13-Rα2 models.
Breast cancer biomarkers at key points during disease progression
High Affinity For IL-13-Rα2
The antibody hu08 binds IL-13-Rα2 with high affinity. Since this receptor lacks a cytoplasmic domain for signaling, it is an interesting target for internalization studies. The MMAF payload effectively inhibited cell division in our target cells.

Q&As

  1. What distinguishes the mc linker from cleavable linkers?

    A: The mc (maleimidocaproyl) linker is a noncleavable linker. Its cleavage and payload release do not depend on differential plasma vs. cytoplasmic properties. Instead, release occurs after the ADC is internalized and the antibody is degraded to amino acids in the lysosome.

  2. What gene encodes the target antigen for the hu08 antibody?

    A: The target antigen IL-13-Rα2 is encoded by the IL13RA2 gene. This protein is closely related to the IL13RA1 subunit but lacks a cytoplasmic signaling domain and is involved in the internalization of interleukin 13.

View the frequently asked questions answered by Creative Biolabs Support.

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