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DMA4-H228
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Catalog No. TCL-02164
DMA4-H228 is an ionizable cationic lipidoid employed in creating lipid nanoparticles (LNPs) for mRNA delivery in vivo. These LNPs, enriched with DMA4-H228, specifically accumulate in antigen-presenting cells within the mouse spleen. When encapsulating mRNA for ovalbumin, these LNPs activate splenic antigen-presenting cells and elevate serum IFN-α levels in mice. Additionally, in a B16/F10-OVA murine melanoma model, such LNPs reduce tumor volume, increase intratumoral CD8+ T cells, and elevate serum anti-ovalbumin IgG titers.
DMA4-H228
DMA4-H228
😃Good
Catalog No. TCL-02164
DMA4-H228 is an ionizable cationic lipidoid employed in creating lipid nanoparticles (LNPs) for mRNA delivery in vivo. These LNPs, enriched with DMA4-H228, specifically accumulate in antigen-presenting cells within the mouse spleen. When encapsulating mRNA for ovalbumin, these LNPs activate splenic antigen-presenting cells and elevate serum IFN-α levels in mice. Additionally, in a B16/F10-OVA murine melanoma model, such LNPs reduce tumor volume, increase intratumoral CD8+ T cells, and elevate serum anti-ovalbumin IgG titers.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | DMA4-H228 is an ionizable cationic lipidoid employed in creating lipid nanoparticles (LNPs) for mRNA delivery in vivo. These LNPs, enriched with DMA4-H228, specifically accumulate in antigen-presenting cells within the mouse spleen. When encapsulating mRNA for ovalbumin, these LNPs activate splenic antigen-presenting cells and elevate serum IFN-α levels in mice. Additionally, in a B16/F10-OVA murine melanoma model, such LNPs reduce tumor volume, increase intratumoral CD8+ T cells, and elevate serum anti-ovalbumin IgG titers. |
| 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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