DiPODS
DiPODS is a thiolate-targeted bioconjugation reagent with irreversible covalent binding activity. DiPODS can rebridge the broken disulfide bonds in antibodies/Fab fragments. DiPODS enables site-specific bioconjugation to generate homogeneous immunoconjugates. DiPODS can conjugate with various payloads via the primary amine at the end of its side chain. DiPODS is applicable to breast cancer-related research.
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- CAS. Nr.: 2756320-37-1
- Formel: C23H32N6O11S2
- Molecular Weight:632.66
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Speicherung:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biologische Aktivität
Beschreibung
In Vitro
FabHER2-DiPODS-FITC (0.8 mg/mL; 30 min) retains specific binding to HER2-positive BT474 human breast cancer cells and exhibits higher immunoreactivity than a non-site-specific lysine-conjugated analogue[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
Chemical Information
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CAS. Nr. 2756320-37-1
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Molecular Weight 632.66
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Formel C23H32N6O11S2
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SMILES
O=C(CCOCCOCCOCCOCCN)NC1=CC(C2=NN=C(S(=O)(C)=O)O2)=CC(C3=NN=C(S(=O)(C)=O)O3)=C1
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Versand
Room temperature in continental US; may vary elsewhere.
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Speicherung
Please store the product under the recommended conditions in the Certificate of Analysis.
Protokoll
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Breast Cancer Modeling
Breast cancer is a heterogeneous cancer, and it has been distinguished into four subtypes: luminal A, luminal B, HER2-positive and basal-like. Molecular mutations, epigenetic alterations, hormone exposure and immune microenvironment are related to the progression of breast cancer.
Reinheit & Dokumentation
Verweise
Calculators
Konzentration (Stammlösung) × Volumen (Stammlösung) = Konzentration (Ziellösung) × Volumen (Ziellösung)