Anti-cyCD79b (clone 10D10)-MCC-DM1 ADC

CAT#: ADC-216LZY

This ADC product is composed of an anti-cyCD79b antibody (clone 10D10) conjugated via MCC linker to DM1 (10D10-MCC-DM1). It has demonstrated a response in non-Hodgkin's lymphoma ofcynomolgus monkey treatment by a MOA (Mechanism of Action) of microtubules depolymerizing.

Gene Expression
Figure 1 IF staining of human cell line REH Figure 2 IHC staining of human lymph node Figure 3 IHC staining of human lymph node Figure 4 IF staining of human cell line A-431 Figure 5 IF staining of human cell line U-2 OS Figure 6 Colon Figure 7 Lymph node Figure 8 RNA cell line category: Cell line enhanced (Daudi, REH, U-698)

Specifications

  • Antibody Overview
  • Mouse/Human Chimeric Anti-cynomolgus monkeyCD79b mAb (10D10)
  • Clone
  • 10D10
  • Linker
  • MCC(Maleimidomethyl cyclohexane-1-carboxylate))
  • Linker Class/Description
  • Class: Noncleavable linker
    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
  • DM1(N2'-deacetyl-N2'-(3-mercapto-1-oxopropyl)-maytansine)
  • Drug Class/Description
  • Class: Maytansinoid
    Description: Maytansinoids are a group of cytotoxins structurally similar to rifamycin, geldanamycin, and ansatrienin. The eponymous natural cytotoxic agent maytansine is a 19-member lactam (ansa
    macrolide) structure originally isolated from the Ethiopian shrub Maytenus ovatus. Maytansinoids can bind to tubulin at or near the vinblastine-binding site, which interfere the formation of microtubules and depolymerize already formed microtubules, inducing mitotic arrest in the intoxicated cells

Target

  • Introduction
  • The B lymphocyte antigen receptor is a multimeric complex that includes the antigen-specific component, surface immunoglobulin (Ig). Surface Ig non-covalently associates with two other proteins, Ig-alpha and Ig-beta, which are necessary for expression and function of the B-cell antigen receptor. This gene encodes the Ig-beta protein of the B-cell antigen component. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
  • Alternative Names
  • CD79B; CD79b molecule, immunoglobulin-associated beta; B29; IGB; AGM6; B-cell antigen receptor complex-associated protein beta chain; Ig-beta; B-cell-specific glycoprotein B29; immunoglobulin-associated B29 protein; CD79b antigen (immunoglobulin-associated beta);
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Breast cancer biomarkers at key points during disease progression
Ideal For Cross-Species Study
This chimeric anti-cynomolgus monkey CD79b antibody is perfect for our cross-species reactivity studies. The 10D10 clone binds effectively to the target, and the conjugation to DM1 allowed us to assess the efficacy of microtubule depolymerization in non-human primate cell models relevant to non-Hodgkin's lymphoma.
Breast cancer biomarkers at key points during disease progression
Stable MCC Linker Performance
The MCC linker used in this conjugate is noncleavable, which was a requirement for our study design. We needed to ensure that the release of the cytotoxic DM1 occurred only after internalization and lysosomal degradation. The product performed reliably, showing good stability and specific activity in our assays.

Q&As

  1. What species reactivity does the 10D10 clone exhibit?

    A: The 10D10 antibody clone is specific for cynomolgus monkey CD79b. It is a mouse/human chimeric antibody designed for research involving non-human primate models, particularly for studies related to non-Hodgkin's lymphoma in cynomolgus monkeys.

  2. What is the stability of the MCC linker?

    A: The MCC linker is a noncleavable linker. It is designed to be stable in the bloodstream, preventing premature release of the payload. The release of the cytotoxic drug occurs only after the ADC is internalized and degraded within the lysosomal compartment of the target cell.

View the frequently asked questions answered by Creative Biolabs Support.

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