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Lipid C16-C
Catalog No. TCL-02360 Copy Product Info
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Lipid C16-C is an ionizable cationic lipid utilized in creating lipid nanoparticles (LNPs) for mRNA delivery both in vitro and in vivo. LNPs with lipid C16-C are preferentially directed to the liver and spleen in mice over other organs such as the lungs, kidneys, lymph nodes, and heart. These LNPs, when encapsulating mRNA for HER2-targeting chimeric antigen receptor (CAR), prompt CAR expression in human macrophages ex vivo and have shown to induce cytotoxic effects in HER2-expressing SKOV3 ovarian cancer cells in vitro.
Lipid C16-C
Copy Product Info🥰Excellent
Catalog No. TCL-02360
Lipid C16-C is an ionizable cationic lipid utilized in creating lipid nanoparticles (LNPs) for mRNA delivery both in vitro and in vivo. LNPs with lipid C16-C are preferentially directed to the liver and spleen in mice over other organs such as the lungs, kidneys, lymph nodes, and heart. These LNPs, when encapsulating mRNA for HER2-targeting chimeric antigen receptor (CAR), prompt CAR expression in human macrophages ex vivo and have shown to induce cytotoxic effects in HER2-expressing SKOV3 ovarian cancer cells in vitro.
Lipid C16-C
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
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
Chemical Properties
Storage & Solubility Information
| Description | Lipid C16-C is an ionizable cationic lipid utilized in creating lipid nanoparticles (LNPs) for mRNA delivery both in vitro and in vivo. LNPs with lipid C16-C are preferentially directed to the liver and spleen in mice over other organs such as the lungs, kidneys, lymph nodes, and heart. These LNPs, when encapsulating mRNA for HER2-targeting chimeric antigen receptor (CAR), prompt CAR expression in human macrophages ex vivo and have shown to induce cytotoxic effects in HER2-expressing SKOV3 ovarian cancer cells in vitro. |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year |
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In Vivo Formulation Calculator (Clear solution)
Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, and a total of 10 animals are to be administered, using a formulation of 
10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.Stock Solution Preparation:
Dissolve 2 mg of the compound in 100 μL DMSO to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
Preparation of the In Vivo Formulation:
1) Add 100 μL of the DMSO stock solution to 400 μL PEG300 and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O and mix thoroughly until a homogeneous solution is obtained.
This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
Dose Conversion
You can also refer to dose conversion for different animals. More Dose Conversion
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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