Anti-Mesothelin (MDX-1382)-Duocarmycins ADC (MDX-1204)
CAT#: ADC-L013
This ADC product is composed of an anti-mesothelin antibody (MDX-1382) conjuagated to Duocarmycins (MDX-1382-Duocarmycins). It has demonstrated a response in ovarian and pancreatic cancers treatment by a MOA (Mechanism of Action) of Bind to DNA minor groove and cause DNA damage.
Specifications
- Antibody Overview
- Fully human IgG1 monoclonal antibody that binds to mesothelin
- Clone
- MDX-1382
- Antibody Conjugation
- Human
- Linker
- cleavable di-peptide linker
- Linker Class/Description
- Peptide linkers, belonging to Enzymatically cleavable linkers, combine greater systemic stability with rapid enzymatic release of the drug in the target cell. The scission of peptidic bonds relies on lysosomal proteolytic enzymes, which have very low activities in blood due to endogenous inhibitors and the unfavorably high pH value of blood.
- Drug
- Duocarmycins
- Drug Class/Description
- Duocarmycins belong to the minor-groove-binding DNA-alkylating agents (DNA MGBA). The natural duocarmycins are isolated from the culture broth of Streptmyces sp and a series of derivatives has also been synthesized
Target
- Introduction
- This gene encodes a preproprotein that is proteolytically processed to generate two protein products, megakaryocyte potentiating factor and mesothelin. Megakaryocyte potentiating factor functions as a cytokine that can stimulate colony formation of bone marrow megakaryocytes. Mesothelin is a glycosylphosphatidylinositol-anchored cell-surface protein that may function as a cell adhesion protein. This protein is overexpressed in epithelial mesotheliomas, ovarian cancers and in specific squamous cell carcinomas. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed.
- Alternative Names
- MPF; SMRP
- Gene ID
- 10232
- UniProt ID
- Q13421
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Q&As
-
What is the mechanism of action for the Duocarmycins payload?
A: Duocarmycins belong to the class of minor-groove-binding DNA-alkylating agents. They bind to the minor groove of DNA and cause DNA damage. The natural forms are isolated from Streptomyces, and they are distinct from tubulin inhibitors.
-
How does the cleavable peptide linker function in this ADC?
A: The peptide linker combines systemic stability with rapid enzymatic release. The scission of the peptidic bonds relies on lysosomal proteolytic enzymes. These enzymes have very low activity in the blood due to endogenous inhibitors and pH, ensuring the drug is released only in the target cell.
View the frequently asked questions answered by Creative Biolabs Support.
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Datasheet
MSDS
COA
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