Your shopping cart is currently empty

eGFP(cy5) mRNA is a chemically modified synthetic mRNA designed for high-sensitivity tracking of gene delivery processes. The compound features a dual-functional design: its nucleotide sequence encodes the enhanced Green Fluorescent Protein (eGFP) to quantify translation efficiency, while the mRNA backbone is covalently labeled with the near-infrared fluorophore Cy5. This dual-labeling system enables researchers to distinguish the physical distribution of mRNA (uptake/endocytosis, visualized as Cy5 red signal) from its functional biological activity (protein expression, visualized as eGFP green signal) at the single-cell level. It is widely utilized in lipid nanoparticle (LNP) formulation optimization, endocytic pathway elucidation, and tissue distribution studies.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 100 μg | Inquiry | Inquiry | Inquiry | |
| 100 μg * 10 | Inquiry | Inquiry | Inquiry |
| Description | eGFP(cy5) mRNA is a chemically modified synthetic mRNA designed for high-sensitivity tracking of gene delivery processes. The compound features a dual-functional design: its nucleotide sequence encodes the enhanced Green Fluorescent Protein (eGFP) to quantify translation efficiency, while the mRNA backbone is covalently labeled with the near-infrared fluorophore Cy5. This dual-labeling system enables researchers to distinguish the physical distribution of mRNA (uptake/endocytosis, visualized as Cy5 red signal) from its functional biological activity (protein expression, visualized as eGFP green signal) at the single-cell level. It is widely utilized in lipid nanoparticle (LNP) formulation optimization, endocytic pathway elucidation, and tissue distribution studies. |
| In vitro | In cancer cell models (e.g., A549, HepG2), eGFP(cy5) mRNA delivered via LNPs allowed for the profiling of endocytic escape; flow cytometry and confocal microscopy revealed that while over 90% of cells were Cy5-positive (indicating successful uptake), only a fraction showed eGFP expression, highlighting the "lost in translation" phenomenon during intracellular trafficking [1][3]. |
| In vivo | In mouse models of lung fibrosis and liver distribution, systemic or local administration of LNP-encapsulated eGFP(cy5) mRNA demonstrated robust accumulation in liver macrophages and lung tissues; Cy5 signals confirmed organ-specific localization, while eGFP fluorescence quantified the extent of functional protein synthesis in different cell types [1][2]. |
| Research Background | Upon transfection into cells, eGFP mRNA enables intracellular expression of enhanced green fluorescent protein (eGFP). The wild-type protein (GFP) was originally discovered in 1962 by Osamu Shimomura from the jellyfish Aequorea victoria. GFP exhibits unique auto-fluorescent properties that require no cofactors or substrates beyond molecular oxygen. Consequently, GFP is frequently fused to proteins of interest to monitor their expression and localization. However, GFP has significant limitations in practical applications. To address these, molecular biologists developed an engineered variant termed eGFP, which maintains identical secondary structure to GFP. Crucially, eGFP incorporates codon optimization for enhanced expression in mammalian cells. |
| Storage | store at low temperature | In solvent: -80°C for 1 year |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
| Size | Quantity | Unit Price | Amount | Operation |
|---|

Copyright © 2015-2026 TargetMol Chemicals Inc. All Rights Reserved.