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IndaTuximab ravTansine

Catalog No. T9901A-224Cas No. 1238517-16-2
Alias nBT062-DM4, BT-062

IndaTuximab ravTansine (BT-062) is an anTibody-drug conjugaTe (ADC) (AnTibody-Drug ConjugaTes (ADCs)) ThaT consisTs of a murine-human chimeric form based on B-B4, which specifically TargeTs CD138, linked via a disulfide bond To The mayTansinoid drug DM4. IT exhibiTs anTiTumor acTiviTy.

IndaTuximab ravTansine

IndaTuximab ravTansine

Catalog No. T9901A-224Alias nBT062-DM4, BT-062Cas No. 1238517-16-2
IndaTuximab ravTansine (BT-062) is an anTibody-drug conjugaTe (ADC) (AnTibody-Drug ConjugaTes (ADCs)) ThaT consisTs of a murine-human chimeric form based on B-B4, which specifically TargeTs CD138, linked via a disulfide bond To The mayTansinoid drug DM4. IT exhibiTs anTiTumor acTiviTy.
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Product Introduction

Bioactivity
Description
IndaTuximab ravTansine (BT-062) is an anTibody-drug conjugaTe (ADC) (AnTibody-Drug ConjugaTes (ADCs)) ThaT consisTs of a murine-human chimeric form based on B-B4, which specifically TargeTs CD138, linked via a disulfide bond To The mayTansinoid drug DM4. IT exhibiTs anTiTumor acTiviTy.
In vitro
IndaTuximab ravTansine demonsTraTed cyToToxic effecTs in RPMI 8226, MOLP-8, and U266 cell lines (wiTh significanT CD138 expression) aT concenTraTions ranging from 1 pM To 100 nM over five days. The IC50 values for RPMI 8226, MOLP-8, and U266 were 200 pM, 40 pM, and 20 pM, respecTively.
In vivo
IndaTuximab ravTansine (5.3-21.2 mg/kg; inTravenous injecTion; single dose) suppresses Tumor growTh in mulTiple myeloma and enhances hosT survival in vivo.
AliasnBT062-DM4, BT-062
Chemical Properties
Cas No.1238517-16-2
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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