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DMG-PEG 2000

SKU: orb1298372

描述

DMG-PEG2000 is a lipid-PEG conjugate used to formulate lipid nanoparticles (LNPs) for nucleic acid delivery. It enhances mucus penetration for oral plasmid DNA delivery in vivo and improves the transfection efficiency of siRNA-loaded liposomes in both in vitro and in vivo research applications.

研究领域

Metabolism Research

图片与验证

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关键属性

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CAS 号160743-62-4
MW2526
纯度≥98% (May vary between batches)
分子式(C2H4O)nC32H62O5
SMILESN.CCCCCCCCCCCCCC(=O)OCC(COCCOC)OC(=O)CCCCCCCCCCCCC
靶点Others,Liposome
溶解性Ethanol:100 mg/mL (39.59 mM);DMSO:60 mg/mL (23.75 mM);10% DMSO+40% PEG300+5% Tween 80+45% Saline:2 mg/mL (0.79 mM)

客户验证数据

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反应性分布

最新实验

3 Results
稀释
样本
摘要
In vitro
Rat
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Lipid nanoparticles (LNPs)
DMG-PEG 2000 is used as a...
In vitro
Mouse
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Lipid nanoparticles (LNPs)
DMG-PEG 2000 is used as a...
In vivo
Mouse
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Lipid nanoparticles (LNPs)
DMG-PEG 2000 is used as a...

生物活性

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体内
METHODS: To study the permeability of NP-3, a single dose of NP-3 (150 μg DNA per mouse) was administered orally to mice. RESULTS: The NP-3 group maintained high luciferase expression in the liver, lung, and intestinal regions within 12 to 24 hours after administration. In addition, NP-3 showed a 1.5-fold higher signal intensity than the NP-1 or NP-2 groups within 12 to 24 hours after oral administration.

储存与操作

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储存-20°C
有效期12 months from date of receipt.
免责声明For research use only

别名

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therapy, T2D, type II diabete, 293T, A549, DMG PEG 2000, DMGPEG 2000, DMG-PEG 2000, DMG-PEG2000, DMG-PEG-2000, HeLa, HepG2, Inhibitor, inhibit, lPEI/DNA nanoparticle, nucleic acid

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关键属性

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实验方案信息

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25 mg
¥ 910.00
50 mg
¥ 1,170.00
100 mg
¥ 1,430.00
发货Usually dispatched within 5-10 working days
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