DC Chemicals

DC49882 · Updated 28 October 2026

cKK-E12

Instructions for Use

Before use

Check the supplied lot number, batch COA, approved SDS, quantity and retest date. Pure form: −20 °C, 1 year; In solvent: −80 °C, 6 months; −20 °C, 1 month. Sealed and protected from light.

For small quantities of viscous or oily lipid, volumetric transfer can reduce weighing losses. Confirm solvent compatibility and solubility before preparing a stock; calculated volumes do not establish solubility.

Stock-solution planning

Volume (mL) = mass (mg) × 1000 / [molecular weight × concentration (mM)].

Mass10 mM20 mM
10 mg1.0064 mL0.5032 mL
25 mg2.5161 mL1.2580 mL
50 mg5.0321 mL2.5161 mL
100 mg10.0642 mL5.0321 mL

Literature formulation reference

ComponentDC Chemicals productMolecular weightMolar ratioMass at 1 µmol total lipid (mg)
cKK-E12DC49882993.62Not assignedNot calculable from disclosed data
DSPCDC57005790.15Not assignedNot calculable from disclosed data
CholesterolDCD-041386.65Not assignedNot calculable from disclosed data
PEG-lipid (identity unassigned)Not uniquely mappedNot establishedNot assignedNot calculable from disclosed data

Main text identifies cKK-E12, DSPC, cholesterol and a PEG-lipid. The complete 2014 SI was not retrieved, so molar ratios, PEG identity/MW, N/P and lipid:RNA mass ratio are not assigned. A familiar 50:10:38.5:1.5 recipe is not assumed to be the verified original formulation.

Read the complete study conditions, biological results, tolerability and figures →

References

  1. Dong Y, Love KT, Dorkin JR et al. Lipopeptide nanoparticles for potent and selective siRNA delivery in rodents and nonhuman primates. PNAS 111, 3955–3960 (2014). DOI: 10.1073/pnas.1322937111.
  2. Correction: additional funding acknowledgments. PNAS 111, 5753 (2014). DOI: 10.1073/pnas.1404711111.