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Sacituzumab (Powder)

(Synonyms: Sacituzumab, 1796566-95-4) Copy Product Info
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Synonyms: Sacituzumab, 1796566-95-4

Catalog No. T35397P Copy Product Info
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Sacituzumab (Powder) is an antibody inhibitor and a humanized monoclonal antibody targeting trophoblast cell surface antigen 2 (TROP2), serving as a component of the antibody-drug conjugate sacituzumab govitecan, used for research and treatment of TROP2-high-expressing tumors such as triple-negative breast cancer.
Sacituzumab (Powder)
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Pack SizePriceUSA StockGlobal StockQuantity
1 mg$1792 weeks2 weeks
5 mg$5642 weeks2 weeks
10 mg$9022 weeks2 weeks
25 mg$1,3802 weeks2 weeks
50 mg$1,8602 weeks2 weeks
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction

Bioactivity
Description
Sacituzumab (Powder) is an antibody inhibitor and a humanized monoclonal antibody targeting trophoblast cell surface antigen 2 (TROP2), serving as a component of the antibody-drug conjugate sacituzumab govitecan, used for research and treatment of TROP2-high-expressing tumors such as triple-negative breast cancer.
In vitro
Methods: The in vitro activity of Sacituzumab was verified by cell viability assays and antibody-dependent cell-mediated cytotoxicity (ADCC) experiments. Trop-2-positive cervical cancer cells (CVX8, ADX3) and negative cells (ADX2) were incubated with 2 μg/mL Sacituzumab for 72 hours, respectively.
Results: Sacituzumab showed no direct cytotoxicity in the absence of effector cells, but could mediate significant ADCC by peripheral blood lymphocytes against Trop-2-positive cells.[1]
Methods: Trop-2-positive cervical cancer cells (CVX8, ADX3) and negative cells (ADX2) were incubated with 2 μg/mL Sacituzumab for 72 hours.
Results: Its IC₅₀ was 55–68 times higher than that of the ADC, with no direct cytotoxicity in the absence of effector cells; however, it could mediate significant ADCC by peripheral blood lymphocytes against Trop-2-positive cells (57.9%±5.5%).[2]
In vivo
Methods: MDA-MB-468 triple-negative breast cancer cells were inoculated into SCID/NCr mice. Sacituzumab (25 mg/kg, dissolved in physiological saline) was administered by intravenous injection twice weekly for 3 weeks.
Results: Tumor burden was reduced in the treatment group, all mice survived to 60 days, showing significant difference compared with the vehicle control group (P < 0.0001). [3]
SynonymsSacituzumab, 1796566-95-4
Reactivity
Human
Application
Functional assay
FormulationLyophilized from a sterile solution in a buffered formulation system (e.g., phosphate-, citrate-, or amino acid-based). Please refer to the CoA for lot-specific composition.
Endotoxin<1.0 EU/mg
Related Conjugates and Formulations
Conjucates
Unconjugated
Antigen Details
Gene ID
Uniprot ID
TargetTROP2
Antibody Information
IsotypeHuman IgG1 kappa
Recommended Isotype Control
Storage & Solubility Information
Storage-20°C for 1 year Shipping with blue ice/Shipping at ambient temperature.

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Keywords

Related Tags: Sacituzumab (Powder) chemical structure | Sacituzumab (Powder) in vivo | Sacituzumab (Powder) in vitro