DMG-PEG 2000

DMG-PEG 2000 (DMG-PEG2000) 可用于脂质纳米颗粒制备,用于口服质粒 DNA 的体内传递途径,提高纳米颗粒的黏液渗透性和传递效率。它也可用于 siRNA 转染的脂质体的制备,能够提高转染效率。

CAS号

160743-62-4

分子式

C34H69NO6

主要靶点

Others

仅限科研使用

Cat No : CM02245

Print datasheet

Synonyms

DMG-PEG2000



产品信息

DMG-PEG2000 is a lipid excipient that has been used in combination with other lipids in the formation of lipid nanoparticles. Formulations containing DMG-PEG2000 have been used in the development of lipid nanoparticles for the delivery of mRNA-based vaccines.

CAS号 160743-62-4
分子式 C34H69NO6
主要靶点 Others
主要通路 其他
分子量 587.927
纯度 , 此纯度可做参考,具体纯度与批次有关系,可咨询客服
储存条件 Powder: -20°C for 3 years | In solvent: -80°C for 1 year
别名 DMG-PEG2000

溶解度

DMSO:100 mg/mL (Need ultrasonic)

参考文献

1.Tianqi Nie, et al. Surface Coating Approach to Overcome Mucosal Entrapment of DNA Nanoparticles for Oral Gene Delivery of Glucagon-like Peptide 1.ACS Appl Mater Interfaces. 2019 Aug 21;11(33):29593-29603.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量   浓度   体积   分子量 *
=
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The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
×
=
×
C1   V1   C2   V2