N-(2-(2,5-Bis((3-aminopropyl)amino)pentanamido)ethyl)-N,N-dimethyl-2,3-bis((Z)-octadec-9-en-1-yloxy)propan-1-aminium chloride tetrahydrochloride
98%
- Product Code: 215104
CAS:
913194-16-8
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| Density: | Storage Condition: | 2-8°C |
Product Description:
Used in gene delivery and nucleic acid transfection, this compound functions as a cationic lipid transfection reagent. Its structure enables efficient binding and condensation of genetic material such as DNA, RNA, or siRNA, facilitating cellular uptake through endocytosis. The presence of multiple amine groups allows for protonation in acidic environments, promoting endosomal escape via the proton sponge effect, which enhances transfection efficiency. It is particularly effective in non-viral gene therapy research and in vitro gene expression studies due to its low cytotoxicity and high delivery performance in a variety of cell lines. Its biodegradable ether-linked alkyl chains contribute to improved stability and reduced toxicity compared to ester-based lipids. Commonly applied in pharmaceutical development and molecular biology for delivering therapeutic genes or silencing target genes.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 25mg | 10-20 days | ฿35,000.00 |
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N-(2-(2,5-Bis((3-aminopropyl)amino)pentanamido)ethyl)-N,N-dimethyl-2,3-bis((Z)-octadec-9-en-1-yloxy)propan-1-aminium chloride tetrahydrochloride
Used in gene delivery and nucleic acid transfection, this compound functions as a cationic lipid transfection reagent. Its structure enables efficient binding and condensation of genetic material such as DNA, RNA, or siRNA, facilitating cellular uptake through endocytosis. The presence of multiple amine groups allows for protonation in acidic environments, promoting endosomal escape via the proton sponge effect, which enhances transfection efficiency. It is particularly effective in non-viral gene therapy research and in vitro gene expression studies due to its low cytotoxicity and high delivery performance in a variety of cell lines. Its biodegradable ether-linked alkyl chains contribute to improved stability and reduced toxicity compared to ester-based lipids. Commonly applied in pharmaceutical development and molecular biology for delivering therapeutic genes or silencing target genes.
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