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18:0 mPEG750 PE ammonium

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Catalog No. TCl-00443
Alias 474922-77-5

18:0 mPEG750 PE (ammonium) serves as a PEG lipid functional terminal for synthesizing liposomes (LPs) in the design of conjugated polymer nanoparticles. Liposomal nanoparticles (LNPs) featuring biotin modification and carboxyl terminals can couple with other biomolecules. These functionalized nanoparticles are applicable for targeting specific cellular proteins. Utilizing streptavidin as a linker, the biotinylated PEG lipid-conjugated polymer nanoparticles can bind with biotinylated antibodies on cell surface receptors, enabling fluorescence-based imaging and sensing applications.

18:0 mPEG750 PE ammonium

18:0 mPEG750 PE ammonium

😃Good
Catalog No. TCl-00443Alias 474922-77-5
18:0 mPEG750 PE (ammonium) serves as a PEG lipid functional terminal for synthesizing liposomes (LPs) in the design of conjugated polymer nanoparticles. Liposomal nanoparticles (LNPs) featuring biotin modification and carboxyl terminals can couple with other biomolecules. These functionalized nanoparticles are applicable for targeting specific cellular proteins. Utilizing streptavidin as a linker, the biotinylated PEG lipid-conjugated polymer nanoparticles can bind with biotinylated antibodies on cell surface receptors, enabling fluorescence-based imaging and sensing applications.
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Bioactivity
Description
18:0 mPEG750 PE (ammonium) serves as a PEG lipid functional terminal for synthesizing liposomes (LPs) in the design of conjugated polymer nanoparticles. Liposomal nanoparticles (LNPs) featuring biotin modification and carboxyl terminals can couple with other biomolecules. These functionalized nanoparticles are applicable for targeting specific cellular proteins. Utilizing streptavidin as a linker, the biotinylated PEG lipid-conjugated polymer nanoparticles can bind with biotinylated antibodies on cell surface receptors, enabling fluorescence-based imaging and sensing applications.
Alias474922-77-5
Chemical Properties
Molecular Weight750(Average)
Formula(C2H4O)nC43H84NO10P.H3N
Storage & Solubility Information
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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
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 μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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2 Enter the in vivo formulation:
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